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EDITORIAL article

Front. Physiol., 28 August 2024
Sec. Avian Physiology
This article is part of the Research Topic The Role of the Pancreas in Poultry View all 6 articles

Editorial: The role of the pancreas in poultry

  • 1Moscow Timiryazev Agricultural Academy, Moscow, Russia
  • 2All-Russian Scientific Research and Technological Institute of Poultry, Russian Academy of Agricultural Sciences, Moscow, Russia

Editorial on the Research Topic
The role of the pancreas in poultry

The pancreas in poultry secretes continuously a secretion that hydrolyzes proteins, fats and carbohydrates to monomers that can be absorbed into the blood (Batoev, 2001; Batoev, 2018; Berdnikov et al., 2009). Both during fasting and after a meal, pancreatic secretion is regulated by nervous and hormonal pathways (Pavlov, 1951). Feeding serves as a powerful stimulator of pancreatic secretion. The period of reflex phase regulation of pancreatic secretion in broiler chickens begins in the first minutes of feed intake and lasts up to 90 min from the moment of feeding (Vertiprakhov et al., 2018). At this time, the regulation of the pancreas is provided reflexively, and the feed consumed by the bird ends up in the goiter or stomach, and pancreatic juice is intensively secreted into the intestine under the influence of impulses arriving via parasympathetic fibers from the digestive center in the medulla oblongata, where they come from the receptors of the oral cavity (Vertiprakhov and Egorov, 2016). In this case, depending on the strength of the stimulus acting on oral receptors, the level of pancreatic secretion changes, i.e., this period is conditioned by gustatory sensations from the quality of feed. Feed intake increases pancreatic juice secretion 2–3 times compared to the preprandial period (Vertiprakhov and Ovchinnikova; Vertiprakhov et al.).

Studies on chickens and other birds have shown that the avian gustatory system consists of taste buds that are not assembled in papillae but are located mostly (60%) in the upper palate, hidden in the crevices of salivary ducts (Liu et al., 2018). Chickens appear to have an acute sense of taste that allows them to distinguish food amino acids, fatty acids, sugars, quinine, calcium and salt among others. A chemosensory system linked to the enteroendocrine system has been found in the gastrointestinal tract and hypothalamus of birds that mediates a dialog between the gut and the brain relevant to the control of food intake (Cheled-Shoval et al., 2015; Niknafs and Roura, 2018). Experimental data using real-time PCR showed the expression of taste receptor genes in chickens. The expression of these genes suggests the involvement of taste pathways for the perception of carbohydrates, amino acids and bitter compounds in the gastrointestinal tract of chickens. Umami taste is one of the five basic taste qualities, along with sweet, bitter, sour, and salty, and is determined by several amino acids and their salts, including monocalic glutamate (MPG) (Yoshida et al., 2015). The fact that the secretory function of the pancreas in chickens responds to flavor additives to feed is proved by experiments on birds with pancreatic duct fistula (Vertiprakhov, 2022). Thus, the presence of receptors in the bird’s mouth cavity is the beginning of the reflex arc, which is directed to the medulla oblongata and determines the reflex phase of digestion regulation, which lasts from 0 to 60–90 min after feeding in chickens (Vertiprakhov, 2022).

The neurohumoral phase of regulation of pancreatic secretion begins 60–90 min after feeding (Vertiprakhov and Borisenko, 2019), which is associated with the release of secretin and cholecystokinin in the intestine when acidic food enters the intestine from the stomach, which stimulate the release of pancreatic juice and its enzymes (DeGolier et al., 1999). In ducks, a peptide that activates pituitary receptors has been found to be involved in regulation (Wang and Cui, 2007). In the brainstem, vagovagal enteropancreatic reflexes can be modulated by incoming signals from higher brain centers, in particular, the hypothalamic-cholinergic system, with tonic stimulation of preganglionary neurons of the dorsal motor nucleus of the vagus nerve, which affects the function of the pancreas (Singer and Niebergall-Roth, 2009).

The role of pancreatic enzymes in animal blood in the regulation of pancreatic secretion is still a matter of debate. The hypothesis of Laporte and Tremolieres (Laporte and Tremolieres, 1971) is interesting in this respect. Trypsin and chymotrypsin in the duodenum were found to have an inhibitory effect on pancreatic enzyme secretion in rats (Kuzmina et al.). In addition, the feedback mechanism is mediated by neurons including the cholinergic pathway (Lui et al., 1986). Experiments conducted on chickens showed that 60 min after feeding, serum trypsin activity increased, while amylase and lipase activities remained at preprandial levels (Vertiprakhov and Grozina, 2018). A correlation was found in the postprandial period: trypsin levels in the postprandial period increased simultaneously in intestine and blood, in parallel with nitric oxide levels, indicating the participation of pancreatic enzymes in the regulation of pancreatic secretory function in poultry (Fisinin et al., 2018; Vertiprakhov and Ovchinnikova). The increase in trypsin activity closely correlates with the content of deposited NO in blood, which indicates the participation of trypsin in the processes of metabolic regulation in animals and humans along with the parasympathetic nervous system.

It is known that pancreatic juice entering the duodenum contains two pools of enzymes: newly synthesized and reconstituted (Vertiprakhov et al., 2016). The rate of enzyme synthesis does not keep up with exosecretion, which was shown when considering the enzyme-secretory activity of the pancreas (Rothman et al., 2002). Consequently, deficits in enzyme synthesis are compensated for by enzyme reduction. The data on the presence of active digestive enzymes in poultry blood were confirmed by biochemical studies.

The results of the experiment on poultry differ significantly from the data obtained on rats (Laporte and Tremolieres, 1971; Korotko and Baibekova, 1989), which showed an inverse relationship between the content of trypsin in blood and pancreatic juice. Specific bipolar islet-acinar cells with secretory and endocrine function, detected by ultrastructural analysis of the secretory cycle (Permyakov et al., 1973), suggest the possibility of simultaneous entry of trypsinogen into both the pancreatic duct and the bloodstream.

The pancreas performs endocrine function with the involvement of hormones such as insulin and glucagon. Insulin is synthesized in β-cells of the pancreas (Moore and Cooper, 1991; Norton et al., 2022). Insulin secretion is related to metabolic rate in broilers (Vertiprakhov et al., 2023). Tissue metabolism has shown a unique effect of insulin on amino acid metabolism (Qaid et al., 2016).

Insulin is a hormone produced by the pancreas in response to high blood glucose levels. It plays a crucial role in the regulation of glucose metabolism in the body (Saltiel and Kahn, 2001). In chickens, insulin has been shown to have several effects, including the following.

1) Glucose uptake: insulin stimulates the transport of glucose from the bloodstream into cells. In chickens, this is especially important for muscle cells, which use a lot of glucose for energy production during movement and growth (Qaid et al., 2016).

2) Lipid metabolism: insulin also regulates lipid metabolism in chickens by promoting the accumulation of excess fat in adipose tissue and inhibiting the breakdown of stored fat for energy (Saltiel and Kahn, 2001).

3) Growth and development: insulin is a key regulator of chick growth and development, especially in the early stages of life. It promotes cell division and differentiation, resulting in increased muscle and bone growth (Hill and Milner, 1985).

4) Reproduction: insulin also plays a role in reproduction in birds by regulating steroid hormone production and supporting oocyte development (Sliwowska et al., 2014).

Conclusion

The pancreas is an unpaired parenchymatous organ belonging to glands of mixed secretion, simultaneously performing exocrine and endocrine functions, as well as participating in the regulation of carbohydrate, protein and fat metabolism in tissues. The exocrine (secretory) part of the pancreas produces digestive juice with enzymes (trypsin, lipase, amylase, proteases, etc.), which enter the duodenal lumen through its exit ducts, subsequently entering the blood, where they perform the role of hormone-like substances in the regulation of metabolism, which is confirmed by the expression of trypsin in many organs and tissues, as well as the presence of special PAR-receptors.

Author contributions

VV: Writing–original draft, Project administration, Methodology. AG: Writing–review and editing, Validation, Software, Conceptualization. VF: Writing–review and editing, Supervision, Resources, Investigation.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

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.

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Keywords: trypsin, pancreas, poultry, taste sensations, feed nutrition

Citation: Vertiprakhov V, Grozina A and Fisinin V (2024) Editorial: The role of the pancreas in poultry. Front. Physiol. 15:1463203. doi: 10.3389/fphys.2024.1463203

Received: 11 July 2024; Accepted: 20 August 2024;
Published: 28 August 2024.

Edited and reviewed by:

Krystyna Pierzchała-Koziec, University of Agriculture in Krakow, Poland

Copyright © 2024 Vertiprakhov, Grozina and Fisinin. 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: Vladimir Vertiprakhov, vertiprakhov63@mail.ru

Disclaimer: 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.