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ERRATUM article

Front. Pharmacol., 31 August 2022
Sec. Gastrointestinal and Hepatic Pharmacology

Erratum: Dihydromyricetin-encapsulated liposomes inhibit exhaustive exercise-induced liver inflammation by orchestrating M1/M2 macrophage polarization

  • Frontiers Media SA, Lausanne, Switzerland

An Erratum on
Dihydromyricetin-encapsulated liposomes inhibit exhaustive exercise-induced liver inflammation by orchestrating M1/M2 macrophage polarization

by Zhou X, Yi L, Lang H, Zhang J, Zhang Q, Yu L, Zhu J and Mi M (2022). Front. Pharmacol. 13:887263. doi: 10.3389/fphar.2022.887263

Due to a production error, there was a mistake in Figure 1 as published. An incorrect version of Figure 1P was used in the original article. The corrected Figure 1 appears below.

FIGURE 1
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FIGURE 1. DHM administration ameliorated EE-induced liver inflammation and its efficacy was influenced by the dosing interval (A) Schematic diagram of the experimental design (B) The body weights of the mice were recorded (C) The liver index represents the ratio of liver weight to body weight (D–G) Serum levels of ALT, AST, GGT, and TBIL were examined (H–M) The expression of the inflammatory cytokines TNF-α, IL-1β, and IL-6 in mouse serum samples (H–J) and mouse liver samples (K–M) was examined by ELISA (N–O) The mRNA expression levels of Tnfa and Il1b were detected by qRT–PCR (P) Liver inflammation was examined by H&E and IHC for TNF-α and IL-1β (Q–S) The expression of the inflammatory cytokines TNF-α, IL-1β, and IL-6 in mouse liver samples was examined by ELISA. Data are presented as the mean ± SEM (n = 5). *p < 0.05, **p < 0.01, compared to the control group; #p < 0.05, ##p < 0.01, compared to the EE group. Scale bar, 100 μm.

The publisher apologizes for this mistake. The original version of this article has been updated.

Keywords: dihydromyricetin, exhaustive exercise, liposome, liver inflammation, macrophage polarization

Citation: Frontiers Production Office (2022) Erratum: Dihydromyricetin-encapsulated liposomes inhibit exhaustive exercise-induced liver inflammation by orchestrating M1/M2 macrophage polarization. Front. Pharmacol. 13:1003574. doi: 10.3389/fphar.2022.1003574

Received: 26 July 2022; Accepted: 26 July 2022;
Published: 31 August 2022.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

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