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REVIEW article

Front. Microbiol., 11 March 2022
Sec. Food Microbiology
This article is part of the Research Topic The interplay between food and intestinal microbiota: How they impact on the well-being status of the host View all 7 articles

Polysaccharide Regulation of Intestinal Flora: A Viable Approach to Maintaining Normal Cognitive Performance and Treating Depression

\r\nXinzhou WangXinzhou Wang1Lu Cheng*Lu Cheng2*Yanan LiuYanan Liu1Ruilin ZhangRuilin Zhang1Zufang WuZufang Wu1Peifang WengPeifang Weng1Peng Zhang,*Peng Zhang1,3*Xin Zhang*\r\nXin Zhang1*
  • 1Department of Food Science and Engineering, Ningbo University, Ningbo, China
  • 2Department of Food Science, Rutgers, The State University of New Jersey, Newark, NJ, United States
  • 3Department of Student Affairs, Xinyang Normal University, Xinyang, China

The intestinal tract of a healthy body is home to a large variety and number of microorganisms that will affect every aspect of the host’s life. In recent years, polysaccharides have been found to be an important factor affecting intestinal flora. Polysaccharides are widely found in nature and play a key role in the life activities of living organisms. In the intestinal tract of living organisms, polysaccharides have many important functions, such as preventing the imbalance of intestinal flora and maintaining the integrity of the intestinal barrier. Moreover, recent studies suggest that gut microbes can influence brain health through the brain-gut axis. Therefore, maintaining brain health through polysaccharide modulation of gut flora deserves further study. In this review, we outline the mechanisms by which polysaccharides maintain normal intestinal flora structure, as well as improving cognitive function in the brain via the brain-gut axis by virtue of the intestinal flora. We also highlight the important role that gut microbes play in the pathogenesis of depression and the potential for treating depression through the use of polysaccharides to modulate the intestinal flora.

Introduction

So far, gut microbiota has been studied for decades. There is a large amount of experimental data confirming the key role of gut microbes in a living organism and calling the gut microbiome “the second genome of the human body” (Zhu et al., 2010), which shows the importance of intestinal flora is greatly recognized in academic circles. Nowadays, research on the association of intestinal flora with various diseases has developed rapidly, such as cancer, type 2 diabetes, and even neurodegenerative diseases (Liu et al., 2018; Sanchez-Alcoholado et al., 2020; Shi et al., 2020). Therefore, in addition to traditional treatment, the regulation of intestinal flora has become a new option for the treatment of related diseases. There are many factors that influence gut microbiology, such as age, antibiotic therapy, and diet (Rinninella et al., 2019), among which dietary factors occupy a significant position and have received the most widespread social attention. The influence of diet on intestinal flora is huge; different nutrients in different foods can promote the growth of some microorganisms in the intestine and inhibit the growth of others (Zmora et al., 2019). The study noted that the fecal microbiota of Italian children on a Western diet pattern consisted mainly of Salmonella and Escherichia. Still, the fecal microbiota of South American children on a traditional plant-based diet pattern consisted mainly of Prevotella enterotype (Conlon and Bird, 2014). In recent years, researchers have found that polysaccharides, either in food ingredients or artificially extracted from specific plants, play an important role in regulating intestinal flora and can provide effective treatment for related diseases.

Polysaccharides are widely found in nature, primarily in plants, animals, and microorganisms (Yang et al., 2020; Barnes et al., 2021; Cai et al., 2021; Murayama and Sugiura, 2021). Humans can obtain polysaccharides by ingesting the corresponding foods and obtain energy through a series of digestion and absorption, such as the starch in cereal foods, which is a critical source of energy (Lovegrove et al., 2017). After scientists’ unremitting research, the antioxidant, anti-aging and immunity-regulating functions of polysaccharides have been widely used (Tian et al., 2020; Ren et al., 2021). In addition to these well-known functions of polysaccharides, scientists have found that polysaccharides and intestinal microorganisms have an interactive relationship. Not all polysaccharides consumed from food can be digested and absorbed by the body. Some of the non-digestible but fermentable polysaccharides are used by intestinal microorganisms to produce various metabolites, such as short-chain fatty acids (SCFAs) (Ahmadi et al., 2017). SCFAs, as the main metabolites of intestinal microorganisms, occupy a critical position in intestinal physiology (Ahmadi et al., 2017; Dupraz et al., 2021). After several years of research, the role of SCFAs has not only been limited to regulating the body’s metabolism but also been found to play an essential role in gut-brain communication (van de Wouw et al., 2018; Silva et al., 2020).

With the progress and development of science, many experiments have demonstrated the interaction between gut microorganisms and the brain (Martin et al., 2018). In a study, the pathogenesis of irritable bowel syndrome (IBS) well demonstrated a bidirectional effect between the nervous system and the gut (Shaidullov et al., 2021). The central nervous system (CNS) in IBS patients might have abnormalities in processing signals from the intestine, and researchers found that a therapeutic effect could be achieved by regulating the patient’s intestinal flora (Mayer et al., 2014). In an experiment on germ-free (GF) mice, it was found that most chemicals in the blood of GF mice were synthesized by intestinal microorganisms and that these chemicals could affect the behavior and neuroendocrine response of GF mice (Galland, 2014). In addition, researchers have found that gut microbes contribute to brain development (Galland, 2014; Mohajeri et al., 2018). Therefore, regulation of intestinal flora becomes a viable new approach for the treatment of related brain disorders (Zhu et al., 2020). Typical diseases include cognitive dysfunction and depression, and scientists have likewise discovered a link between gut flora and these disorders and suggested the possibility of treating them by regulating gut flora (Galland, 2014; Mohajeri et al., 2018).

The mystery of using polysaccharides to regulate the gut microbiota to maintain normal cognitive function in the brain and improve depression has been gradually unraveled by scientists in recent years. This provides a new approach to treating depression and maintaining normal cognitive function. In this review, we review scientific findings on the regulation of gut microbial structure by polysaccharides, the utilization of polysaccharides by gut microbes, and the effects of gut microbes on the brain via the brain-gut axis. In addition, we will further explore the potential of modulating gut microbiota through polysaccharides to treat depression and maintain normal cognitive performance and provide an outlook on the development of this method in the future.

Polysaccharides and the Effect of Polysaccharides on Intestinal Microbiota

Polysaccharides

The structure of polysaccharides is relatively complex, and natural polysaccharides are composed of many monosaccharide residues, which are interconnected by oligosaccharide bonds (Cui, 2005; Verma et al., 2019). Although the structure of polysaccharides is very complex, with the development of science and technology, we have clarified the molecular structure of a part of polysaccharides and the related sugar units that make up polysaccharides (Cui, 2005). From the source, polysaccharides can be divided into plant polysaccharides, animal polysaccharides, and microbial polysaccharides (Verma et al., 2019). For instance, starch is a common polysaccharide in life, which is derived from rice, are polymerized from glucose (Li and Gilbert, 2018). Starch usually includes amylose and amylopectin, the difference between which is that amylose has a small number of long-chain branches and low molecular weights, while amylopectin has a large number of short-chain branches and high molecular weights (Li and Gilbert, 2018). Natural polysaccharides have the advantages of being non-toxic, stable, and easy to obtain, and are valued by various fields (Li and Gilbert, 2018). Nowadays, in addition to the functional foods we know, polysaccharides have a wide range of applications (Dai et al., 2021; Qi et al., 2021). With the further exploration of polysaccharide functions, polysaccharides have been used for treating related diseases, such as obesity and type 2 diabetes (Wu et al., 2019; Chen et al., 2020). In recent years, scientists have also discovered that polysaccharides have the ability to regulate the structure of intestinal flora and protect intestinal health (Ahmadi et al., 2017). These findings open a new door to the study of polysaccharides. Researches on polysaccharides are continuing, and more potential will be explored in the future.

Utilization of Polysaccharides by the Intestinal Microbiota

Some polysaccharides obtained from the outside world cannot be digested and absorbed by the human body. These polysaccharides can be divided into two categories: fermentable and unfermentable. In contrast, unfermentable polysaccharides will eventually be discharged as waste, and fermentable polysaccharides can be degraded by intestinal microorganisms and eventually absorbed and used by the human body (Ahmadi et al., 2017). Previous research have pointed out some polysaccharides are required to be degradated by intestinal microorganisms for further utilization, such as resistant starch, levan, and mannan (Ye et al., 2020). Among the identified intestinal microorganisms, some of them are thought to be able to utilize polysaccharides, which they degrade by producing the corresponding enzymes (Bernalier-Donadille, 2010; Cockburn and Koropatkin, 2016), such as Bacteroides. Bacteroides occupy a large proportion of the intestinal microorganisms and are able to produce large amounts of carbohydrate-active enzymes (CAZymes) (Hemsworth et al., 2016; Ye et al., 2020). The researchers have found that CAZymes can degrade various polysaccharides and form fermentable monosaccharides, which facilitates the eventual absorption and utilization of polysaccharides by the body (Ye et al., 2020). Studies have demonstrated that certain intestinal microorganisms can provide themselves with a carbon source by fermenting polysaccharides, which will facilitate the production of important metabolites by intestinal microorganisms, such as SCFAs (Yao et al., 2020a). The utilization of polysaccharides by intestinal microorganisms is shown in Figure 1. SCFAs are important metabolites of intestinal microorganisms (Yao et al., 2020a); they are composed of a small hydrocarbon chain and a carboxylic acid moiety; the common SCFAs include butyric acid, acetic acid, propionic acid, etc. (Correa-Oliveira et al., 2016). SCFAs are relevant to our health. Studies have proven that SCAFs have weight loss and hypoglycemic effects, and can be used to treat obesity and type 2 diabetes (Murugesan et al., 2018; Sanna et al., 2019), as well as to regulate immune cell function and enhance immunity (Correa-Oliveira et al., 2016; Yao et al., 2020b). Moreover, in a recent study, researchers found that SCFAs also played an important role in the microbe-gut-brain axis (Dalile et al., 2019). The impact of SCFAs on microbial-gut-brain communication is dramatic (Dalile et al., 2019; Silva et al., 2020). In the past, a large number of studies have demonstrated that SCFAs can act on free fatty acid receptor 2 (FFAR2) and free fatty acid receptor 3 (FFAR3); among them, FFAR2 is mainly expressed in immune cells, and FFAR3 is mainly expressed in the sympathetic nervous system (Dalile et al., 2019). In addition, SCFAs also affect brain function by acting on the CNS, and based on this, researchers have found that SCFAs can relieve chronic psychological stress and have a therapeutic effect on related neurological disorders, such as depression and Parkinson’s disease (PD) (van de Wouw et al., 2018; Shin et al., 2020; Silva et al., 2020). With the continuous development of science and technology, the research on the utilization of polysaccharides by intestinal flora and the function of their metabolites will be further developed in the future.

FIGURE 1
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Figure 1. Utilization of polysaccharides by intestinal microorganisms.

Shaping of Intestinal Flora by Polysaccharides

Among the many factors that influence the structure of the intestinal flora, diet is considered to be the easiest one to manipulate and most likely to reshape the intestinal flora. Polysaccharides, as part of the daily diet, also have a regulatory effect on the structure of the intestinal flora (Ho Do et al., 2021). The human body has to consume a certain amount of carbohydrates every day. Because the human body lacks the corresponding enzymes, some of the complex carbohydrates cannot be digested and absorbed by the body (Xu et al., 2013; Ho Do et al., 2021). As a representative of complex carbohydrates, part of polysaccharides can serve as an essential source of nutrients for intestinal microorganisms and influence the growth of related intestinal microorganisms, and thus regulating the structure of intestinal flora (Xu et al., 2013). In addition, polysaccharides also promotes the production of metabolites by intestinal microorganisms, which in turn changes the living environment of microorganisms, further shaping the structure of the intestinal flora (Xu et al., 2013). For example, Li et al. (2019) shown that the structure of the intestinal flora of rats could be significantly changed by adding a certain amount of grifola frondosa polysaccharides to the feed. In another experiment, Xu et al. (2017) used Ganoderma lucidum polysaccharides (GLP) to treat mice with intestinal flora disorders due to a high-fat diet and found that the treatment with GLP increased the abundance of Enterococcus in the intestines of the mice, which had a moderating effect on the intestinal flora structure of the mice. In addition, a large number of similar experiments have confirmed the shaping effect of polysaccharides on the structure of intestinal flora. For example, the study on coix polysaccharides found that it could promote the proliferation of Lactobacillus and Bifidobacterium in the intestine and increase the total amount of SCFAs, thus changing the structure of intestinal flora (Yin et al., 2018). In another experiment, researchers found by simulating gastrointestinal digestion and fermentation that Pleurotus eryngii polysaccharide (PEP) could not be digested by the gastrointestinal tract, but could be metabolized and utilized by intestinal microorganisms and produce the metabolites SCFAs, which also indicated that modulation of PEP polysaccharides could change the composition structure of intestinal microorganisms, as shown by a significant increase in the relative abundance of Firmicutes (Ma et al., 2021). Moreover, the ocean also contains many polysaccharides that we can study and use, and among them, seaweed polysaccharides have been studied most extensively. A study on brown seaweed showed that polysaccharides extracted from brown seaweed can be metabolized by intestinal microorganisms to produce SCFAs, and that the abundance of the phylum Firmicutes and Bacteroidetes was significantly increased in the intestine after brown seaweed polysaccharides modulation (Chen et al., 2018). Summarizing the above experimental results, we can easily conclude that polysaccharides that are not digested by the gastrointestinal tract but are fermentable can regulate the composition of the intestinal microorganisms. The role of polysaccharides in shaping the intestinal flora structure is still under investigation, and regulating the structure of the intestinal flora through the use of polysaccharides will be applied in an increasing number of fields in the future.

Gut Microbiota’s Function: Maintaining Normal Cognitive Function Through the Brain-Gut Axis

The Role of Intestinal Microbes in the Brain-Gut Axis

Studies have confirmed that there are at least three parallel channels between the gut microbes and the CNS that keep them in communication, involving endocrine, neural, and immune signaling mechanisms. According to the results obtained so far, it has been found that the gut microbes regulate the CNS mainly through neuroendocrine and neuroimmune mechanisms and that the vagus nerve plays an important role in this process (Martin et al., 2018). Communication between gut microbes and the CNS is usually mediated by molecules of microbial origin, including the SCFAs, tryptophan metabolites, and secondary bile acids, which mainly transmit signals to enterochromaffin cells (ECCs) and enteroendocrine cells (EECs). These molecules of microbial origin will induce the secretion of intestinal hormones, such as peptide YY (PYY), γ-aminobutyric acid (GABA), glucagon-like peptide 1 (GLP1), and transmits signals to the brain via the vagus nerve or body circulation (Martin et al., 2018; Dalile et al., 2019). A small percentage of molecules of microbial origin also enter the body circulation or cross the blood-brain barrier; however, it is not clear whether these molecules can reach and act directly on the brain (Martin et al., 2018; Dalile et al., 2019). In addition, it has been shown that intestinal microorganisms can indirectly affect the hypothalamic-pituitary-adrenal axis (HPA) through the blood circulating in the body. The HPA axis is closely related to some common psychiatric disorders (Dinan and Cryan, 2017). According to the available research results, the role of gut microbial pairs in the brain-gut axis is shown in Figure 2. To further discover the role played by gut microbes in the brain-gut axis, scientists have conducted numerous additional experiments. IBS has been shown to be caused by altered messages from the gut microbes to the brain, and the brain-gut axis plays a critical role in the pathogenesis of IBS (Mayer et al., 2014). One study found that some IBS cases were associated with changes in the metabolism and microorganisms that bound primary bile acids and proteases produced by intestinal microorganisms (Mayer et al., 2014). Moreover, extensive experimental evidence has shown that gut microbes can influence brain development and function through the brain-gut axis (Mayer et al., 2015; Rogers et al., 2016). One study in mice pointed out that altering the gut flora of mice during a certain developmental period affected brain development. In another experiment, functional brain responses were found to be altered in healthy women who consumed probiotics for a long period of time, as evidenced by their reduced response to an emotion recognition task (Mayer et al., 2015). In addition, multiple sclerosis (MS) is also affected by commensal microbes in the gut that act on brain cells, and by studying mouse models of the disease. The scientists found that metabolites from gut microbes altered the behavior of microglia in the brain, which in turn modulated astrocyte activity to promote or prevent inflammation (Rothhammer et al., 2018). The role of gut microbes in the brain-gut axis is undoubtedly enormous. Based on this, scientists are proposing more and more treatments for neurological diseases by regulating gut flora. Some of these methods have already been applied, and some need to be explored more.

FIGURE 2
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Figure 2. The role of gut microbial pairs in the brain-gut axis.

The Relationship Between Gut Microbes and Cognitive Performance and Improvement of Cognitive Performance Through Regulation of Gut Flora

As research continues to advance, it is increasingly recognized that intestinal flora plays an important role in the communication between the intestine and the brain. Therefore, there are more and more researches aiming at improving brain function by regulating intestinal flora. In recent years, it has been found that intestinal flora has a close connection with the cognitive ability of the brain, and regulating intestinal flora can play a certain role in improving cognitive ability (Davidson et al., 2018; Go et al., 2021; Kim et al., 2021). Cognitive abilities usually refer to the human brain’s ability to extract, store and process information, including imagination, memory, learning, and analytical ability (Lovden et al., 2020). Cognitive ability is a predictor of a society’s economic success, and the longevity and health of its members are an important part of the response to a society’s good or bad fortune (Lovden et al., 2020). Scientists have done a lot of research in the field of improving cognitive ability, and improving cognitive ability by regulating intestinal flora is a very promising direction. A large amount of experimental data suggests that the early life of an organism is an important period of gut microbial colonization and that affecting this period in some way will lead to changes in the structure of the organism’s gut flora, leading to certain effects on its cognitive abilities. For instance, the ability of bird to learn to sing will be affected by restricting the nutritional intake of birds, thus altering the composition structure of the microorganisms in their gut (Davidson et al., 2018). A growing number of experiments have demonstrated that regulating intestinal flora is effective in improving cognitive deterioration. The study of Ni et al. (2019) found that the use of probiotics, such as Bifidobacterium and Lactobacillus, had a significant effect on the regulation of intestinal flora and was effective in enhancing cognitive abilities, including learning and memory, in the elderly.

Diet is an important factor influencing gut flora, and there is a large amount of experimental data demonstrating that regulating gut flora through diet can have an impact on the cognitive ability of the brain (Zhang et al., 2020; Romanenko et al., 2021). In one experiment, researchers altered the intestinal flora of mice by changing their diet and found that mice fed a diet with beef had a significant improvement in memory, while another experiment showed that a diet high in sucrose led to impaired cognitive flexibility in mice (Leigh and Morris, 2020). In an experiment by Kang et al. (2014), they investigated the effects of exercise and a high-fat diet on the intestinal flora of mice and the effects of changes in intestinal flora on cognitive function, and the results showed that both exercise and a high-fat diet would have a significant effect on the composition of intestinal microorganisms, including the Bacteroidetes and Firmicutes, which are the most predominant in the intestine, and found that changes in intestinal flora through exercise could significantly improve cognitive decline due to dysbiosis caused by a high-fat diet. In addition, the researchers found that the regulation of intestinal flora by polysaccharides could greatly improve cognitive performance. Su et al. (2018) found that the composition of intestinal microorganisms in the mice treated with Flammulina velutipes polysaccharides (FVP) was significantly altered compared to the control group, as evidenced by an increase in the abundance of Actinobacteria, Erysipelotrichia, and Bacteroidia, and a decrease in the abundance of Clostridia, and that the FVP treated mice exhibited better learning and memory abilities. In another experiment, researchers found that Cistanche deserticola polysaccharides could inhibit oxidative stress and peripheral inflammation by restoring intestinal flora homeostasis due to D-galactose-induced aging in a mouse model, thereby improving cognitive function in mice (Gao et al., 2021). There are many other similar studies; for example, a polysaccharide extracted from Astragalus membranaceus has been shown to treat cognitive impairment by altering the intestinal flora of diabetic mice (Liu et al., 2019). The method of improving cognitive ability by regulating intestinal flora has received significant attention and will be applied in more and more fields.

As the role of intestinal flora in brain-gut communication becomes more apparent, researchers have found a strong link between intestinal flora and Alzheimer’s disease (AD) (Vogt et al., 2017). AD is a progressive neurodegenerative disease and a major cause of dementia. Patients with AD have significantly impaired cognitive abilities, which can manifest as memory loss and dramatic changes in daily behavior (MahmoudianDehkordi et al., 2019; Askarova et al., 2020). Until now, there has been no particularly good treatment for AD (MahmoudianDehkordi et al., 2019). This suggests that our understanding of AD still needs to be further developed. Based on the critical role that gut microbes play in the brain-gut axis, scientists are turning their attention to preventing and treating AD by regulating gut microbes (Xu and Wang, 2016; El Sayed et al., 2021). Studies have confirmed that AD pathology is characterized by extracellular plaques composed of amyloid-β peptides and intracellular neurofibrillary tangles composed of hyperphosphorylated tau protein. Based on the pathogenesis of AD, researchers have found that modulating gut microbes can affect brain amyloid deposition by studying AD mouse models (Jiang et al., 2017; Bostanciklioglu, 2019). In addition, the researchers found significant changes in intestinal flora diversity in AD patients, including decreases in the Firmicutes and Bifidobacterium and an increase in Bacteroidetes (Vogt et al., 2017). By using a comprehensive computational approach, the experiment demonstrated that the metabolites of intestinal microorganisms in humans might be an important mechanistic link between environmental exposure and various aspects of AD (Xu and Wang, 2016). In addition, experiments by MahmoudianDehkordi et al. (2019) similarly found a strong link between gut microbes and AD. It was found that serum concentrations of primary bile acids were lower in AD patients compared to normal elderly, while secondary bile acids, deoxycholic acid and its conjugated forms, produced by intestinal microbial metabolism, were higher. As the experiment progressed, the researchers found that the higher the levels of these secondary conjugated bile acids, the worse the cognitive function. Many experiments can give us some insight that the role played by intestinal microorganisms and their metabolites in the brain-gut axis have a certain influence on the pathogenesis of AD, and we can purposefully regulate the composition of the intestinal flora or influence the production of intestinal microbial metabolites to prevent the pathogenesis of AD, and the exploration of this field needs to be further advanced.

Given the important role of gut microorganisms in the brain-gut axis and the regulatory role of diet on gut flora, we can propose the hypothesis that the regulatory effect on gut flora can be achieved by changing the structure of the diet, such as increasing the intake of polysaccharides in the diet, and then improving cognitive performance and preventing some common diseases of cognitive decline through the effect of gut flora and its metabolites on the brain-gut axis. The regulation of gut flora as a new approach to improve cognitive performance has great scope for exploration in the future.

Polysaccharides, Gut Microbiota, and Depression

The Relationship Between Gut Microbiota and Depression

Depression is one of the most common mental illnesses in everyday life and poses a serious health risk (LeMoult and Gotlib, 2019). Depression is often thought to be related to the regulation of neurotransmitters. To date, the causes of depression remain poorly understood, and multiple factors are involved in the development of depression (Malhi and Mann, 2018). Given the key role that gut microbes play in the brain-gut axis, scientists have identified a strong link between gut microbes and depression (Huang and Wu, 2021). According to the summary of a large amount of experimental data, the composition of gut microorganisms in depressed patients was significantly different compared to healthy controls in terms of the composition of gut microorganisms (Guo et al., 2019; Averina et al., 2020). The intestinal microbial diversity of depressed patients showed a significant decrease; more specifically, Ruminococcus, Bifidobacterium, Faecalibacterium, and Lactobacillus in the intestine of patients were at a lower level, and the level of Proteobacteria and Bacteroides was higher (Averina et al., 2020; Du et al., 2020), as illustrated in Figure 3. In general, there is a significant increase in harmful microorganisms and a decrease in beneficial microorganisms in the gut of depressed patients (Averina et al., 2020). The role played by gut microbes in the brain-gut axis has been mentioned above, and the metabolites produced by gut microbes can act as signaling substances to influence brain function. A study by Huang and Wu (2021) showed that gut microbes have a modulatory effect on brain neurotransmitters, and this modulation may have a role in the treatment of depression. In addition, in another experiment, researchers transplanted fecal flora from depressed patients into the intestines of GF mice and found that the mice showed depressive behavior, suggesting that changes in intestinal flora would lead to depression (Liu et al., 2020).

FIGURE 3
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Figure 3. Differences in intestinal flora between depressed and healthy people.

As we age, there is a certain aging of the intestinal flora in the human body, which is also associated with the development of depression (Linnemann and Lang, 2020). It was found that the core gut flora of older people showed some loss and weakness compared to younger people, such as differences in the abundance of Bifidobacteria (O’Toole and Jeffery, 2015; Kurilshikov et al., 2021). As mentioned above, gut flora can use dietary fiber in food to produce important metabolites such as SCFAs, which in turn affect the brain via the brain-gut axis. Thus, aging of the intestinal flora can impair the body’s ability to digest dietary fiber, resulting in malnutrition and neurodegeneration, leading to psychiatric disorders such as depression (Yahfoufi et al., 2020; Konjevod et al., 2021). From this, we can deduce that elderly people are more likely to suffer from depression due to the aging of intestinal flora, and can be prevented and treated by regulating the intestinal flora.

The Interaction of Polysaccharides With Gut Microbiota to Improve Depression

The Health risks of depression are enormous, and a large number of depressed patients around the world participate in depression treatment every year, but the effectiveness of treatment is not obvious, and the withdrawal rate from treatment is very high (Kessler, 2018; Alexopoulos, 2019). The causes of depression are very complex, and according to studies to date, depression has been found to occur mainly in relation to life circumstances, mental state, physical health status, age stage, and genetics (Molenaar et al., 2016; Cepeda et al., 2019; Arias de la Torre et al., 2021; Dall’Aglio et al., 2021). Traditional treatments for depression include medication, electroconvulsive therapy, and some form of psychotherapy. Although these methods can provide some relief from depression, there are still many problems, such as the lack of effectiveness of the treatment for some patients and the unbearable treatment process (Holtzheimer and Nemeroff, 2006). Therefore, scientists hope to find a treatment that is effective and easy to use with few side effects (Cohen and DeRubeis, 2018).

With the continued exploration of gut flora, scientists have found a strong link between gut flora and the onset of depression and have produced some alleviating therapeutic effects on depressed patients by regulating their gut flora (Wu et al., 2020). Among the many factors affecting the structure of intestinal flora, diet is undoubtedly one of the most important factors, and different food components will have different effects on the intestinal flora, among which polysaccharides have received the attention of scientists with the advantages of easy access, little harm, and obvious regulation of intestinal flora (Van den Abbeele et al., 2020; Ho Do et al., 2021). Today, there are many experimental results showing that polysaccharides have the ability to reverse depression-induced dysbiosis of intestinal flora, anti-inflammatory, promote the production of SCFAs, and maintain the integrity of the intestinal barrier, which would contribute to the treatment of depression (Van den Abbeele et al., 2020; Shen et al., 2021; Yan et al., 2021). For instance, Yan et al. found high levels of pro-inflammatory cytokines in the hippocampus and serum of depressed mice and a significant dysregulation of intestinal flora in their experiments (Yan et al., 2020). By using polysaccharides extracted from okra, it was found that it had a significant restorative effect on the intestinal flora of depressed mice, as shown by an upregulation of the proportion of the Firmicutes, as well as a downregulation of the relative proportions of Bacteroidetes and Actinobacteria. This modulation would help to strengthen the intestinal mucosal barrier, as well as maintain normal intestinal immune system function and reduce the inflammatory response in the intestine, which is effective in combating depression, and depressed mice showed some improvement in their depressive symptoms. In addition, the experiment also revealed a significant increase in SCFAs in mice treated with okra polysaccharides, which act as important communication mediators and exert a positive influence on antidepressant disorders. In other experiments, similar results were obtained. Chen et al. (2019) found that a water-soluble polysaccharide from Ginkgo biloba effectively reversed depression-induced gut flora dysbiosis and also increased the abundance of Lactobacillus, thus providing a therapeutic effect on depression.

So far, the research on polysaccharide modulation of intestinal flora for depression is not deep enough, and this field still has very much room for exploration. Thinking further, this method of regulating intestinal flora using polysaccharides can effectively maintain the homeostasis of intestinal flora, prevent the loss and weakening of core intestinal flora, and is more convenient, safer and more acceptable than traditional depression treatments, offering a new possibility for the treatment of depression and allowing more depressed patients to receive reasonable treatment, especially elderly depressed patients. However, it is still too early to make this method widely available, and we need to conduct more in-depth research to ensure the effectiveness of this method. In the future, we can imagine that a special polysaccharide product may appear in our daily life, which can target the regulation of depression-related microorganisms in human intestine, improve the composition structure of intestinal flora, induce relevant intestinal microorganisms to produce beneficial metabolites, and help us prevent or treat depression, and in medical treatment, polysaccharide will also become an effective means to treat depression.

Conclusion

Polysaccharides as a common food ingredient can effectively regulate the composition of microorganisms in the intestine and promote the production of metabolites from intestinal microorganisms. The metabolites of intestinal microorganisms can improve brain function through the brain-gut axis. According to recent experimental results, polysaccharides can effectively treat cognitive decline in the brain and improve depression by regulating intestinal flora, but the current research in this area is not thorough enough. In the future, the effects of polysaccharides on the regulation of gut bacteria and the production of gut microbial metabolites need to be further explored, which may provide a convenient, safe, and efficient treatment option for cognitive improvement and depression treatment.

Author Contributions

XW: conceptualization, validation, and writing–original draft. LC: supervision. YL, ZW, and PW: writing–original draft. RZ: conceptualization. PZ: supervision and writing–original draft. XZ: supervision, writing–review, and editing. All authors contributed to the article and approved the submitted version.

Funding

This work was sponsored by Zhejiang Provincial Key Research and Development Program (2020C02037) and the Ningbo Natural Science Foundation (2021J107).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Abbreviations

SCFAs, short-chain fatty acids; IBS, irritable bowel syndrome; CNS, central nervous system; GF, germ-free; CAZymes, carbohydrate-active enzymes; FFAR2, free fatty acid receptor 2; FFAR3, free fatty acid receptor 3; PD, Parkinson’s disease; GLP, Ganoderma lucidum polysaccharides; ECCs, enterochromaffin cells; EECs, enteroendocrine cells; PYY, peptide YY; GABA, γ-aminobutyric acid; GLP1, glucagon-like peptide 1; HPA, hypothalamic-pituitary-adrenal axis; FVP, Flammulina velutipes polysaccharides; AD, Alzheimer’s disease.

References

Ahmadi, S., Mainali, R., Nagpal, R., Sheikh-Zeinoddin, M., Soleimanian-Zad, S., Wang, S., et al. (2017). Dietary polysaccharides in the amelioration of gut microbiome dysbiosis and metabolic diseases. Obes. Control. Ther. 4. doi: 10.15226/2374-8354/4/2/00140

CrossRef Full Text | Google Scholar

Alexopoulos, G. S. (2019). Mechanisms and treatment of late-life depression. Transl. Psychiatry 9:188. doi: 10.1038/s41398-019-0514-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Arias de la Torre, J., Vilagut, G., Ronaldson, A., Dregan, A., Ricci-Cabello, I., Hatch, S. L., et al. (2021). Prevalence and age patterns of depression in the United Kingdom. A population-based study. J. Affect. Disord. 279, 164–172. doi: 10.1016/j.jad.2020.09.129

PubMed Abstract | CrossRef Full Text | Google Scholar

Askarova, S., Umbayev, B., Masoud, A. R., Kaiyrlykyzy, A., Safarova, Y., Tsoy, A., et al. (2020). The links between the gut microbiome, aging, modern lifestyle and Alzheimer’s disease. Front. Cell. Infect. Microbiol. 10:104. doi: 10.3389/fcimb.2020.00104

PubMed Abstract | CrossRef Full Text | Google Scholar

Averina, O. V., Zorkina, Y. A., Yunes, R. A., Kovtun, A. S., Ushakova, V. M., Morozova, A. Y., et al. (2020). Bacterial metabolites of human gut microbiota correlating with depression. Int. J. Mol. Sci. 21:9234. doi: 10.3390/ijms21239234

PubMed Abstract | CrossRef Full Text | Google Scholar

Barnes, W. J., Koj, S., Black, I. M., Archer-Hartmann, S. A., Azadi, P., Urbanowicz, B. R., et al. (2021). Protocols for isolating and characterizing polysaccharides from plant cell walls: a case study using rhamnogalacturonan-II. Biotechnol. Biofuels 14:142. doi: 10.1186/s13068-021-01992-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Bernalier-Donadille, A. (2010). Fermentative metabolism by the human gut microbiota. Gastroentérol. Clin. Biol. 34, 16–22. doi: 10.1016/S0399-8320(10)70016-6

CrossRef Full Text | Google Scholar

Bostanciklioglu, M. (2019). The role of gut microbiota in pathogenesis of Alzheimer’s disease. J. Appl. Microbiol. 127, 954–967. doi: 10.1111/jam.14264

PubMed Abstract | CrossRef Full Text | Google Scholar

Cai, B., Pan, J., Chen, H., Chen, X., Ye, Z., Yuan, H., et al. (2021). Oyster polysaccharides ameliorate intestinal mucositis and improve metabolism in 5-fluorouracil-treated S180 tumour-bearing mice. Carbohydr. Polym. 256:117545. doi: 10.1016/j.carbpol.2020.117545

PubMed Abstract | CrossRef Full Text | Google Scholar

Cepeda, M. S., Kern, D. M., and Nicholson, S. (2019). Treatment resistant depression in women with peripartum depression. BMC Pregnancy Childbirth 19:323. doi: 10.1186/s12884-019-2462-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, L., Xu, W., Chen, D., Chen, G., Liu, J., Zeng, X., et al. (2018). Digestibility of sulfated polysaccharide from the brown seaweed Ascophyllum nodosum and its effect on the human gut microbiota in vitro. Int. J. Biol. Macromol. 112, 1055–1061. doi: 10.1016/j.ijbiomac.2018.01.183

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, M., Xiao, D., Liu, W., Song, Y., Zou, B., Li, L., et al. (2020). Intake of Ganoderma lucidum polysaccharides reverses the disturbed gut microbiota and metabolism in type 2 diabetic rats. Int. J. Biol. Macromol. 155, 890–902. doi: 10.1016/j.ijbiomac.2019.11.047

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, P., Hei, M., Kong, L., Liu, Y., Yang, Y., Mu, H., et al. (2019). One water-soluble polysaccharide from Ginkgo biloba leaves with antidepressant activities via modulation of the gut microbiome. Food Funct. 10, 8161–8171. doi: 10.1039/c9fo01178a

PubMed Abstract | CrossRef Full Text | Google Scholar

Cockburn, D. W., and Koropatkin, N. M. (2016). Polysaccharide degradation by the intestinal microbiota and its influence on human health and disease. J. Mol. Biol. 428, 3230–3252. doi: 10.1016/j.jmb.2016.06.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Cohen, Z. D., and DeRubeis, R. J. (2018). Treatment selection in depression. Annu. Rev. Clin. Psychol. 14, 209–236. doi: 10.1146/annurev-clinpsy-050817-084746

PubMed Abstract | CrossRef Full Text | Google Scholar

Conlon, M. A., and Bird, A. R. (2014). The impact of diet and lifestyle on gut microbiota and human health. Nutrients 7, 17–44. doi: 10.3390/nu7010017

PubMed Abstract | CrossRef Full Text | Google Scholar

Correa-Oliveira, R., Fachi, J. L., Vieira, A., Sato, F. T., and Vinolo, M. A. (2016). Regulation of immune cell function by short-chain fatty acids. Clin. Transl. Immunology 5:73. doi: 10.1038/cti.2016.17

PubMed Abstract | CrossRef Full Text | Google Scholar

Cui, S. (2005). Structural analysis of polysaccharides. Food Carbohydr. doi: 10.1201/9780203485286.ch3

CrossRef Full Text | Google Scholar

Dai, L., Xi, X., Li, X., Li, W., Du, Y., Lv, Y., et al. (2021). Self-assembled all-polysaccharide hydrogel film for versatile paper-based food packaging. Carbohydr. Polym. 271:118425. doi: 10.1016/j.carbpol.2021.118425

PubMed Abstract | CrossRef Full Text | Google Scholar

Dalile, B., Van Oudenhove, L., Vervliet, B., and Verbeke, K. (2019). The role of short-chain fatty acids in microbiota-gut-brain communication. Nat. Rev. Gastroenterol. Hepatol. 16, 461–478. doi: 10.1038/s41575-019-0157-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Dall’Aglio, L., Lewis, C. M., and Pain, O. (2021). Delineating the genetic component of gene expression in major depression. Biological. Psychiatry 89, 627–636. doi: 10.1016/j.biopsych.2020.09.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Davidson, G. L., Cooke, A. C., Johnson, C. N., and Quinn, J. L. (2018). The gut microbiome as a driver of individual variation in cognition and functional behaviour. Philos. Trans. R. Soc. Lond. B Biol. Sci. 373:20170286. doi: 10.1098/rstb.2017.0286

PubMed Abstract | CrossRef Full Text | Google Scholar

Dinan, T. G., and Cryan, J. F. (2017). Brain-gut-microbiota axis and mental health. Psychosom. Med. 79, 920–926. doi: 10.1097/PSY.0000000000000519

PubMed Abstract | CrossRef Full Text | Google Scholar

Du, Y., Gao, X. R., Peng, L., and Ge, J. F. (2020). Crosstalk between the microbiota-gut-brain axis and depression. Heliyon 6:e04097. doi: 10.1016/j.heliyon.2020.e04097

PubMed Abstract | CrossRef Full Text | Google Scholar

Dupraz, L., Magniez, A., Rolhion, N., Richard, M. L., Da Costa, G., Touch, S., et al. (2021). Gut microbiota-derived short-chain fatty acids regulate IL-17 production by mouse and human intestinal gammadelta T cells. Cell Rep. 36:109332. doi: 10.1016/j.celrep.2021.109332

PubMed Abstract | CrossRef Full Text | Google Scholar

El Sayed, N. S., Kandil, E. A., and Ghoneum, M. H. (2021). Enhancement of Insulin/PI3K/Akt signaling pathway and modulation of gut microbiome by probiotics fermentation technology, a kefir grain product, in sporadic Alzheimer’s disease model in mice. Front. Pharmacol. 12:666502. doi: 10.3389/fphar.2021.666502

PubMed Abstract | CrossRef Full Text | Google Scholar

Galland, L. (2014). The gut microbiome and the brain. J. Med. Food 17, 1261–1272. doi: 10.1089/jmf.2014.7000

PubMed Abstract | CrossRef Full Text | Google Scholar

Gao, Y., Li, B., Liu, H., Tian, Y., Gu, C., Du, X., et al. (2021). Cistanche deserticola polysaccharides alleviate cognitive decline in aging model mice by restoring the gut microbiota-brain axis. Aging (Albany NY) 13, 15320–15335. doi: 10.18632/aging.203090

PubMed Abstract | CrossRef Full Text | Google Scholar

Go, J., Chang, D. H., Ryu, Y. K., Park, H. Y., Lee, I. B., Noh, J. R., et al. (2021). Human gut microbiota Agathobaculum butyriciproducens improves cognitive impairment in LPS-induced and APP/PS1 mouse models of Alzheimer’s disease. Nutr. Res. 86, 96–108. doi: 10.1016/j.nutres.2020.12.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Guo, Y., Xie, J. P., Deng, K., Li, X., Yuan, Y., Xuan, Q., et al. (2019). Prophylactic effects of bifidobacterium adolescentis on anxiety and depression-like phenotypes after chronic stress: a role of the gut microbiota-inflammation axis. Front. Behav. Neurosci. 13:126. doi: 10.3389/fnbeh.2019.00126

PubMed Abstract | CrossRef Full Text | Google Scholar

Hemsworth, G. R., Dejean, G., Davies, G. J., and Brumer, H. (2016). Learning from microbial strategies for polysaccharide degradation. Biochem. Soc. Trans. 44, 94–108. doi: 10.1042/BST20150180

PubMed Abstract | CrossRef Full Text | Google Scholar

Ho Do, M., Seo, Y. S., and Park, H. Y. (2021). Polysaccharides: bowel health and gut microbiota. Crit. Rev. Food Sci. Nutr. 61, 1212–1224. doi: 10.1080/10408398.2020.1755949

PubMed Abstract | CrossRef Full Text | Google Scholar

Holtzheimer, P. E., and Nemeroff, C. B. (2006). Advances in the treatment of depression. NeuroRX 3, 42–56. doi: 10.1016/j.nurx.2005.12.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Huang, F., and Wu, X. (2021). Brain neurotransmitter modulation by gut microbiota in anxiety and depression. Front. Cell Dev. Biol. 9:649103. doi: 10.3389/fcell.2021.649103

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiang, C., Li, G., Huang, P., Liu, Z., and Zhao, B. (2017). The gut microbiota and Alzheimer’s disease. J. Alzheimers Dis. 58, 1–15. doi: 10.3233/JAD-161141

PubMed Abstract | CrossRef Full Text | Google Scholar

Kang, S. S., Jeraldo, P. R., Kurti, A., Miller, M. E. B., Cook, M. D., Whitlock, K., et al. (2014). Diet and exercise orthogonally alter the gut microbiome and reveal independent associations with anxiety and cognition. Mol. Neurodegener. 9:36. doi: 10.1186/1750-1326-9-36

PubMed Abstract | CrossRef Full Text | Google Scholar

Kessler, R. C. (2018). The potential of predictive analytics to provide clinical decision support in depression treatment planning. Curr. Opin. Psychiatry. 31, 32–39. doi: 10.1097/YCO.0000000000000377

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, C. S., Cha, L., Sim, M., Jung, S., Chun, W. Y., Baik, H. W., et al. (2021). Probiotic supplementation improves cognitive function and mood with changes in gut microbiota in community-dwelling older adults: a randomized, double-blind, placebo-controlled, multicenter trial. J. Gerontol. A. Biol. Sci. Med. Sci. 76, 32–40. doi: 10.1093/gerona/glaa090

PubMed Abstract | CrossRef Full Text | Google Scholar

Konjevod, M., Nikolac Perkovic, M., Sáiz, J., Svob Strac, D., Barbas, C., and Rojo, D. (2021). Metabolomics analysis of microbiota-gut-brain axis in neurodegenerative and psychiatric diseases. J. Pharmaceut. Biomed. 194:113681. doi: 10.1016/j.jpba.2020.113681

PubMed Abstract | CrossRef Full Text | Google Scholar

Kurilshikov, A., Medina-Gomez, C., Bacigalupe, R., Radjabzadeh, D., Wang, J., Demirkan, A., et al. (2021). Large-scale association analyses identify host factorsinfluencing human gut microbiome composition. Nat. Genet. 53, 156–165. doi: 10.1038/s41588-020-00763-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Leigh, S. J., and Morris, M. J. (2020). Diet, inflammation and the gut microbiome: mechanisms for obesity-associated cognitive impairment. Biochim. Biophys. Acta Mol. Basis. Dis. 1866, 165767. doi: 10.1016/j.bbadis.2020.165767

PubMed Abstract | CrossRef Full Text | Google Scholar

LeMoult, J., and Gotlib, I. H. (2019). Depression: a cognitive perspective. Clin. Psychol. Rev. 69, 51–66. doi: 10.1016/j.cpr.2018.06.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, H., and Gilbert, R. G. (2018). Starch molecular structure: the basis for an improved understanding of cooked rice texture. Carbohydr. Polym. 195, 9–17. doi: 10.1016/j.carbpol.2018.04.065

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, L., Guo, W. L., Zhang, W., Xu, J. X., Qian, M., Bai, W. D., et al. (2019). Grifola frondosa polysaccharides ameliorate lipid metabolic disorders and gut microbiota dysbiosis in high-fat diet fed rats. Food Funct. 10, 2560–2572. doi: 10.1039/c9fo00075e

PubMed Abstract | CrossRef Full Text | Google Scholar

Linnemann, C., and Lang, U. E. (2020). Pathways connecting late-life depression and dementia. Front. Pharmacol. 11:279. doi: 10.3389/fphar.2020.00279

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, G., Liang, L., Yu, G., and Li, Q. (2018). Pumpkin polysaccharide modifies the gut microbiota during alleviation of type 2 diabetes in rats. Int. J. Biol. Macromol. 115, 711–717. doi: 10.1016/j.ijbiomac.2018.04.127

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, S., Guo, R., Liu, F., Yuan, Q., Yu, Y., and Ren, F. (2020). Gut microbiota regulates depression-like behavior in rats through the neuroendocrine-immune-mitochondrial pathway. Neuropsychiatr. Dis. Treat. 16, 859–869. doi: 10.2147/NDT.S243551

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, Y., Liu, W., Li, J., Tang, S., Wang, M., Huang, W., et al. (2019). A polysaccharide extracted from Astragalus membranaceus residue improves cognitive dysfunction by altering gut microbiota in diabetic mice. Carbohydr. Polym. 205, 500–512. doi: 10.1016/j.carbpol.2018.10.041

PubMed Abstract | CrossRef Full Text | Google Scholar

Lovden, M., Fratiglioni, L., Glymour, M. M., Lindenberger, U., and Tucker-Drob, E. M. (2020). Education and cognitive functioning across the life span. Psychol. Sci. Public Interest 21, 6–41. doi: 10.1177/1529100620920576

PubMed Abstract | CrossRef Full Text | Google Scholar

Lovegrove, A., Edwards, C. H., De Noni, I., Patel, H., El, S. N., Grassby, T., et al. (2017). Role of polysaccharides in food, digestion, and health. Crit. Rev. Food Sci. Nutr. 57, 237–253. doi: 10.1080/10408398.2014.939263

PubMed Abstract | CrossRef Full Text | Google Scholar

Ma, G., Xu, Q., Du, H., Muinde Kimatu, B., Su, A., Yang, W., et al. (2021). Characterization of polysaccharide from Pleurotus eryngii during simulated gastrointestinal digestion and fermentation. Food Chem. 370:131303. doi: 10.1016/j.foodchem.2021.131303

PubMed Abstract | CrossRef Full Text | Google Scholar

MahmoudianDehkordi, S., Arnold, M., Nho, K., Ahmad, S., Jia, W., Xie, G., et al. (2019). Altered bile acid profile associates with cognitive impairment in Alzheimer’s disease—An emerging role for gut microbiome. Alzheimers Dement. 15, 76–92. doi: 10.1016/j.jalz.2018.07.217

PubMed Abstract | CrossRef Full Text | Google Scholar

Malhi, G. S., and Mann, J. J. (2018). Depression. Lancet 392, 2299–2312. doi: 10.1016/s0140-6736(18)31948-2

CrossRef Full Text | Google Scholar

Martin, C. R., Osadchiy, V., Kalani, A., and Mayer, E. A. (2018). The brain-gut-microbiome axis. Cell. Mol. Gastroenterol. Hepatol. 6, 133–148. doi: 10.1016/j.jcmgh.2018.04.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Mayer, E. A., Savidge, T., and Shulman, R. J. (2014). Brain-gut microbiome interactions and functional bowel disorders. Gastroenterology 146, 1500–1512. doi: 10.1053/j.gastro.2014.02.037

PubMed Abstract | CrossRef Full Text | Google Scholar

Mayer, E. A., Tillisch, K., and Gupta, A. (2015). Gut/brain axis and the microbiota. J. Clin. Invest. 125, 926–938. doi: 10.1172/JCI76304

PubMed Abstract | CrossRef Full Text | Google Scholar

Mohajeri, M. H., La Fata, G., Steinert, R. E., and Weber, P. (2018). Relationship between the gut microbiome and brain function. Nutr. Rev. 76, 481–496. doi: 10.1093/nutrit/nuy009

PubMed Abstract | CrossRef Full Text | Google Scholar

Molenaar, D., Middeldorp, C. M., Willemsen, G., Ligthart, L., Nivard, M. G., and Boomsma, D. I. (2016). Evidence for gender-dependent genotype by environment interaction in adult depression. Behav. Genet. 46, 59–71. doi: 10.1007/s10519-015-9752-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Murayama, S., and Sugiura, Y. (2021). “Origin of soil polysaccharides, and ectomycorrhizal fungal sclerotia as sources of forest soil polysaccharides,” in Sclerotia Grains in Soils: A New Perspective from Pedosclerotiology, ed. M. Watanabe (Singapore: Springer), doi: 10.1007/978-981-33-4252-1_6

CrossRef Full Text | Google Scholar

Murugesan, S., Nirmalkar, K., Hoyo-Vadillo, C., Garcia-Espitia, M., Ramirez-Sanchez, D., and Garcia-Mena, J. (2018). Gut microbiome production of short-chain fatty acids and obesity in children. Eur. J. Clin. Microbiol. Infect. Dis. 37, 621–625. doi: 10.1007/s10096-017-3143-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Ni, Y., Yang, X., Zheng, L., Wang, Z., Wu, L., Jiang, J., et al. (2019). Lactobacillus and Bifidobacterium improves physiological function and cognitive ability in aged mice by the regulation of gut microbiota. Mol. Nutr. Food Res. 63:e1900603. doi: 10.1002/mnfr.201900603

PubMed Abstract | CrossRef Full Text | Google Scholar

O’Toole, P. W., and Jeffery, I. B. (2015). Gut microbiota and aging. Science 350, 1214–1215. doi: 10.1126/science.aac8469

PubMed Abstract | CrossRef Full Text | Google Scholar

Qi, X., Tong, X., Pan, W., Zeng, Q., You, S., and Shen, J. (2021). Recent advances in polysaccharide-based adsorbents for wastewater treatment. J. Clean. Prod. 315:128221. doi: 10.1016/j.jclepro.2021.128221

CrossRef Full Text | Google Scholar

Ren, L., Zhang, J., and Zhang, T. (2021). Immunomodulatory activities of polysaccharides from Ganoderma on immune effector cells. Food Chem. 340:127933. doi: 10.1016/j.foodchem.2020.127933

PubMed Abstract | CrossRef Full Text | Google Scholar

Rinninella, E., Raoul, P., Cintoni, M., Franceschi, F., Miggiano, G. A. D., Gasbarrini, A., et al. (2019). What is the healthy gut microbiota composition? A changing ecosystem across age, environment, diet, and diseases. Microorganisms 7:14. doi: 10.3390/microorganisms7010014

PubMed Abstract | CrossRef Full Text | Google Scholar

Rogers, G. B., Keating, D. J., Young, R. L., Wong, M. L., Licinio, J., and Wesselingh, S. (2016). From gut dysbiosis to altered brain function and mental illness: mechanisms and pathways. Mol. Psychiatry 21, 738–748. doi: 10.1038/mp.2016.50

PubMed Abstract | CrossRef Full Text | Google Scholar

Romanenko, M., Kholin, V., Koliada, A., and Vaiserman, A. (2021). Nutrition, gut microbiota, and Alzheimer’s disease. Front. Psychiatry 12:712673. doi: 10.3389/fpsyt.2021.712673

PubMed Abstract | CrossRef Full Text | Google Scholar

Rothhammer, V., Borucki, D. M., Tjon, E. C., Takenaka, M. C., Chao, C.-C., Ardura-Fabregat, A., et al. (2018). Microglial control of astrocytes in response to microbial metabolites. Nature 557, 724–728. doi: 10.1038/s41586-018-0119-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Sanchez-Alcoholado, L., Ordonez, R., Otero, A., Plaza-Andrade, I., Laborda-Illanes, A., Medina, J. A., et al. (2020). Gut microbiota-mediated inflammation and gut permeability in patients with obesity and colorectal cancer. Int. J. Mol. Sci. 21:6782. doi: 10.3390/ijms21186782

PubMed Abstract | CrossRef Full Text | Google Scholar

Sanna, S., van Zuydam, N. R., Mahajan, A., Kurilshikov, A., Vich Vila, A., Vosa, U., et al. (2019). Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases. Nat. Genet. 51, 600–605. doi: 10.1038/s41588-019-0350-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Shaidullov, I. F., Sorokina, D. M., Sitdikov, F. G., Hermann, A., Abdulkhakov, S. R., and Sitdikova, G. F. (2021). Short chain fatty acids and colon motility in a mouse model of irritable bowel syndrome. BMC Gastroenterol. 21:37. doi: 10.1186/s12876-021-01613-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Shen, F., Song, Z., Xie, P., Li, L., Wang, B., Peng, D., et al. (2021). Polygonatum sibiricum polysaccharide prevents depression-like behaviors by reducing oxidative stress, inflammation, and cellular and synaptic damage. J. Ethnopharmacol. 275:114164. doi: 10.1016/j.jep.2021.114164

PubMed Abstract | CrossRef Full Text | Google Scholar

Shi, H., Wang, Q., Zheng, M., Hao, S., Lum, J. S., Chen, X., et al. (2020). Supplement of microbiota-accessible carbohydrates prevents neuroinflammation and cognitive decline by improving the gut microbiota-brain axis in diet-induced obese mice. J. Neuroinflammation 17:77. doi: 10.1186/s12974-020-01760-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Shin, C., Lim, Y., Lim, H., and Ahn, T. B. (2020). Plasma short-chain fatty acids in patients with Parkinson’s disease. Mov. Disord. 35, 1021–1027. doi: 10.1002/mds.28016

PubMed Abstract | CrossRef Full Text | Google Scholar

Silva, Y. P., Bernardi, A., and Frozza, R. L. (2020). The role of short-chain fatty acids from gut microbiota in gut-brain communication. Front. Endocrinol. (Lausanne) 11:25. doi: 10.3389/fendo.2020.00025

PubMed Abstract | CrossRef Full Text | Google Scholar

Su, A., Yang, W., Zhao, L., Pei, F., Yuan, B., Zhong, L., et al. (2018). Flammulina velutipes polysaccharides improve scopolamine-induced learning and memory impairment in mice by modulating gut microbiota composition. Food Funct. 9, 1424–1432. doi: 10.1039/c7fo01991b

PubMed Abstract | CrossRef Full Text | Google Scholar

Tian, H., Liu, H., Song, W., Zhu, L., Zhang, T., Li, R., et al. (2020). Structure, antioxidant and immunostimulatory activities of the polysaccharides from Sargassum carpophyllum. Algal Res. 49:101853. doi: 10.1016/j.algal.2020.101853

CrossRef Full Text | Google Scholar

van de Wouw, M., Boehme, M., Lyte, J. M., Wiley, N., Strain, C., O’Sullivan, O., et al. (2018). Short-chain fatty acids: microbial metabolites that alleviate stress-induced brain-gut axis alterations. J. Physiol. 596, 4923–4944. doi: 10.1113/jp276431

PubMed Abstract | CrossRef Full Text | Google Scholar

Van den Abbeele, P., Verstrepen, L., Ghyselinck, J., Albers, R., Marzorati, M., and Mercenier, A. (2020). A novel non-digestible, carrot-derived polysaccharide (cRG-I) selectively modulates the human gut microbiota while promoting gut barrier integrity: an integrated in vitro approach. Nutrients 12:1917. doi: 10.3390/nu12071917

PubMed Abstract | CrossRef Full Text | Google Scholar

Verma, A., Tiwari, A., Panda, P. K., Saraf, S., Jain, A., and Jain, S. K. (2019). “Locust bean gum in drug delivery application,” in Natural Polysaccharides in Drug Delivery and Biomedical Applications, eds Md S Hasnain and A. K. Nayak (Cambridge, MA: Academic Press), doi: 10.1016/B978-0-12-817055-7.00008-X

CrossRef Full Text | Google Scholar

Vogt, N. M., Kerby, R. L., Dill-McFarland, K. A., Harding, S. J., Merluzzi, A. P., Johnson, S. C., et al. (2017). Gut microbiome alterations in Alzheimer’s disease. Sci. Rep. 7:13537. doi: 10.1038/s41598-017-13601-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, M., Tian, T., Mao, Q., Zou, T., Zhou, C. J., Xie, J., et al. (2020). Associations between disordered gut microbiota and changes of neurotransmitters and short-chain fatty acids in depressed mice. Transl. Psychiatry 10:350. doi: 10.1038/s41398-020-01038-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, T. R., Lin, C. S., Chang, C. J., Lin, T. L., Martel, J., Ko, Y. F., et al. (2019). Gut commensal Parabacteroides goldsteinii plays a predominant role in the anti-obesity effects of polysaccharides isolated from Hirsutella sinensis. Gut 68, 248–262. doi: 10.1136/gutjnl-2017-315458

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, R., and Wang, Q. Q. (2016). Towards understanding brain-gut-microbiome connections in Alzheimer’s disease. BMC Syst. Biol. 10:63. doi: 10.1186/s12918-016-0307-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, S., Dou, Y., Ye, B., Wu, Q., Wang, Y., Hu, M., et al. (2017). Ganoderma lucidum polysaccharides improve insulin sensitivity by regulating inflammatory cytokines and gut microbiota composition in mice. J. Funct. Foods 38, 545–552. doi: 10.1016/j.jff.2017.09.032

CrossRef Full Text | Google Scholar

Xu, X., Xu, P., Ma, C., Tang, J., and Zhang, X. (2013). Gut microbiota, host health, and polysaccharides. Biotechnol. Adv. 31, 318–337. doi: 10.1016/j.biotechadv.2012.12.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Yahfoufi, N., Matar, C., and Ismail, N. (2020). Adolescence and aging: impact of adolescence inflammatory stress and microbiota alterations on brain development, aging, and neurodegeneration. J. Gerontol. A-Biol. 75, 1251–1257. doi: 10.1093/gerona/glaa006

PubMed Abstract | CrossRef Full Text | Google Scholar

Yan, T., Nian, T., Liao, Z., Xiao, F., Wu, B., Bi, K., et al. (2020). Antidepressant effects of a polysaccharide from okra (Abelmoschus esculentus (L) Moench) by anti-inflammation and rebalancing the gut microbiota. Int. J. Biol. Macromol. 144, 427–440. doi: 10.1016/j.ijbiomac.2019.12.138

PubMed Abstract | CrossRef Full Text | Google Scholar

Yan, T., Wang, N., Liu, B., Wu, B., Xiao, F., He, B., et al. (2021). Schisandra chinensis ameliorates depressive-like behaviors by regulating microbiota-gut-brain axis via its anti-inflammation activity. Phytother. Res. 35, 289–296. doi: 10.1002/ptr.6799

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, X., Li, A., Li, X., Sun, L., and Guo, Y. (2020). An overview of classifications, properties of food polysaccharides and their links to applications in improving food textures. Trends Food Sci. Technol. 102, 1–15. doi: 10.1016/j.tifs.2020.05.020

CrossRef Full Text | Google Scholar

Yao, Y., Cai, X., Fei, W., Ye, Y., Zhao, M., and Zheng, C. (2020a). The role of short-chain fatty acids in immunity, inflammation and metabolism. Crit. Rev. Food Sci. Nutr. 62, 1–12. doi: 10.1080/10408398.2020.1854675

PubMed Abstract | CrossRef Full Text | Google Scholar

Yao, Y., Yan, L., Chen, H., Wu, N., Wang, W., and Wang, D. (2020b). Cyclocarya paliurus polysaccharides alleviate type 2 diabetic symptoms by modulating gut microbiota and short-chain fatty acids. Phytomedicine 77:153268. doi: 10.1016/j.phymed.2020.153268

PubMed Abstract | CrossRef Full Text | Google Scholar

Ye, M., Yu, J., Shi, X., Zhu, J., Gao, X., and Liu, W. (2020). Polysaccharides catabolism by the human gut bacterium -Bacteroides thetaiotaomicron: advances and perspectives. Crit. Rev. Food Sci. Nutr. 61, 3569–3588. doi: 10.1080/10408398.2020.1803198

PubMed Abstract | CrossRef Full Text | Google Scholar

Yin, H. M., Wang, S. N., Nie, S. P., and Xie, M. Y. (2018). Coix polysaccharides: gut microbiota regulation and immunomodulatory. Bioact. Carbohydr. Diet. Fibre 16, 53–61. doi: 10.1016/j.bcdf.2018.04.002

CrossRef Full Text | Google Scholar

Zhang, M., Zhao, D., Zhou, G., and Li, C. (2020). Dietary pattern, gut microbiota, and Alzheimer’s disease. J. Agric. Food Chem. 68, 12800–12809. doi: 10.1021/acs.jafc.9b08309

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, B., Wang, X., and Li, L. (2010). Human gut microbiome: the second genome of human body. Protein Cell 1, 718–725. doi: 10.1007/s13238-010-0093-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, S., Jiang, Y., Xu, K., Cui, M., Ye, W., Zhao, G., et al. (2020). The progress of gut microbiome research related to brain disorders. J. Neuroinflammation 17:25. doi: 10.1186/s12974-020-1705-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Zmora, N., Suez, J., and Elinav, E. (2019). You are what you eat: diet, health and the gut microbiota. Nat. Rev. Gastroenterol. Hepatol. 16, 35–56. doi: 10.1038/s41575-018-0061-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: polysaccharides, intestinal flora, brain-gut axis, cognitive, depression

Citation: Wang X, Cheng L, Liu Y, Zhang R, Wu Z, Weng P, Zhang P and Zhang X (2022) Polysaccharide Regulation of Intestinal Flora: A Viable Approach to Maintaining Normal Cognitive Performance and Treating Depression. Front. Microbiol. 13:807076. doi: 10.3389/fmicb.2022.807076

Received: 01 November 2021; Accepted: 21 February 2022;
Published: 11 March 2022.

Edited by:

Erica Pontonio, University of Bari Aldo Moro, Italy

Reviewed by:

Wei Li, Nanjing Agricultural University, China
Rodolfo Sardone, National Institute of Gastroenterology S. de Bellis Research Hospital (IRCCS), Italy

Copyright © 2022 Wang, Cheng, Liu, Zhang, Wu, Weng, Zhang and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Lu Cheng, lc894@scarletmail.rutgers.edu; Peng Zhang, zp017083@163.com; Xin Zhang, zhangxin@nbu.edu.cn

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