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Syzygium cumini Leaf Extract Reverts Hypertriglyceridemia via Downregulation of the Hepatic XBP-1s/PDI/MTP Axis in Monosodium L-Glutamate-Induced Obese Rats

Syzygium cumini is used worldwide for the treatment of metabolic syndrome-associated outcomes. Previously, we described the antihypertriglyceridemic effect of the hydroethanolic extract of S. cumini leaf (HESc) in monosodium L-glutamate- (MSG-) induced obese rats. This study sought to investigate th...

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Autores principales: França, Lucas Martins, Coêlho, Caio Fernando Ferreira, Freitas, Larissa Nara Costa, Souza, Ivana Letícia Santos, Chagas, Vinicyus Teles, Debbas, Victor, de Lima, Thais Martins, de Souza, Heraldo Possolo, Laurindo, Francisco Rafael Martins, Paes, Antonio Marcus de Andrade
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446099/
https://www.ncbi.nlm.nih.gov/pubmed/31015892
http://dx.doi.org/10.1155/2019/9417498
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author França, Lucas Martins
Coêlho, Caio Fernando Ferreira
Freitas, Larissa Nara Costa
Souza, Ivana Letícia Santos
Chagas, Vinicyus Teles
Debbas, Victor
de Lima, Thais Martins
de Souza, Heraldo Possolo
Laurindo, Francisco Rafael Martins
Paes, Antonio Marcus de Andrade
author_facet França, Lucas Martins
Coêlho, Caio Fernando Ferreira
Freitas, Larissa Nara Costa
Souza, Ivana Letícia Santos
Chagas, Vinicyus Teles
Debbas, Victor
de Lima, Thais Martins
de Souza, Heraldo Possolo
Laurindo, Francisco Rafael Martins
Paes, Antonio Marcus de Andrade
author_sort França, Lucas Martins
collection PubMed
description Syzygium cumini is used worldwide for the treatment of metabolic syndrome-associated outcomes. Previously, we described the antihypertriglyceridemic effect of the hydroethanolic extract of S. cumini leaf (HESc) in monosodium L-glutamate- (MSG-) induced obese rats. This study sought to investigate the molecular mechanisms underlying the antihypertriglyceridemic effect of HESc in MSG-obese rats. Newborn male Wistar rats were injected subcutaneously with MSG (4.0 g/kg/day, obese group) or saline 1.25% (1.0 mL/kg/day, lean group), from 2nd through 10th postnatal day. At 8 weeks old, obese rats started to be orally treated with HESc (0.5 or 1.0 g/kg/day, n = 7) or saline 0.9% (1 mL/kg/day, n = 7). Lean rats received saline solution (1 mL/kg/day, n = 7). Upon 8-week treatment, animals were euthanized for blood and tissue collection. Another set of adult nonobese Wistar rats was used for the assessment of HESc acute effects on Triton WR1339-induced hypertriglyceridemia. HESc reduced weight gain, as well as adipose tissue fat pads, without altering food intake of obese rats. HESc restored fasting serum glucose, triglycerides, total cholesterol, and free fatty acids, as well as insulin sensitivity, to levels similar to lean rats. Additionally, HESc halved the triglyceride content into very low-density lipoprotein particles, as well as healed liver steatosis, in obese rats. Hepatic protein expression of the endoplasmic reticulum chaperone GRP94 was decreased by HESc, which also downregulated the hepatic triglyceride secretion pathway by reducing the splicing of X-box binding protein 1 (XBP-1s), as well as protein disulfide isomerase (PDI) and microsomal triglyceride transfer protein (MTP) translational levels. This action was further corroborated by the acute inhibitory effect of HESc on triglyceride accumulation on Triton WR1339-treated rats. Our data support the downregulation of the XBP-1s/PDI/MTP axis in the liver of MSG-obese rats as a novel feasible mechanism for the antihypertriglyceridemic effect promoted by the polyphenolic phytocomplex present in S. cumini leaf.
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spelling pubmed-64460992019-04-23 Syzygium cumini Leaf Extract Reverts Hypertriglyceridemia via Downregulation of the Hepatic XBP-1s/PDI/MTP Axis in Monosodium L-Glutamate-Induced Obese Rats França, Lucas Martins Coêlho, Caio Fernando Ferreira Freitas, Larissa Nara Costa Souza, Ivana Letícia Santos Chagas, Vinicyus Teles Debbas, Victor de Lima, Thais Martins de Souza, Heraldo Possolo Laurindo, Francisco Rafael Martins Paes, Antonio Marcus de Andrade Oxid Med Cell Longev Research Article Syzygium cumini is used worldwide for the treatment of metabolic syndrome-associated outcomes. Previously, we described the antihypertriglyceridemic effect of the hydroethanolic extract of S. cumini leaf (HESc) in monosodium L-glutamate- (MSG-) induced obese rats. This study sought to investigate the molecular mechanisms underlying the antihypertriglyceridemic effect of HESc in MSG-obese rats. Newborn male Wistar rats were injected subcutaneously with MSG (4.0 g/kg/day, obese group) or saline 1.25% (1.0 mL/kg/day, lean group), from 2nd through 10th postnatal day. At 8 weeks old, obese rats started to be orally treated with HESc (0.5 or 1.0 g/kg/day, n = 7) or saline 0.9% (1 mL/kg/day, n = 7). Lean rats received saline solution (1 mL/kg/day, n = 7). Upon 8-week treatment, animals were euthanized for blood and tissue collection. Another set of adult nonobese Wistar rats was used for the assessment of HESc acute effects on Triton WR1339-induced hypertriglyceridemia. HESc reduced weight gain, as well as adipose tissue fat pads, without altering food intake of obese rats. HESc restored fasting serum glucose, triglycerides, total cholesterol, and free fatty acids, as well as insulin sensitivity, to levels similar to lean rats. Additionally, HESc halved the triglyceride content into very low-density lipoprotein particles, as well as healed liver steatosis, in obese rats. Hepatic protein expression of the endoplasmic reticulum chaperone GRP94 was decreased by HESc, which also downregulated the hepatic triglyceride secretion pathway by reducing the splicing of X-box binding protein 1 (XBP-1s), as well as protein disulfide isomerase (PDI) and microsomal triglyceride transfer protein (MTP) translational levels. This action was further corroborated by the acute inhibitory effect of HESc on triglyceride accumulation on Triton WR1339-treated rats. Our data support the downregulation of the XBP-1s/PDI/MTP axis in the liver of MSG-obese rats as a novel feasible mechanism for the antihypertriglyceridemic effect promoted by the polyphenolic phytocomplex present in S. cumini leaf. Hindawi 2019-03-21 /pmc/articles/PMC6446099/ /pubmed/31015892 http://dx.doi.org/10.1155/2019/9417498 Text en Copyright © 2019 Lucas Martins França et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
França, Lucas Martins
Coêlho, Caio Fernando Ferreira
Freitas, Larissa Nara Costa
Souza, Ivana Letícia Santos
Chagas, Vinicyus Teles
Debbas, Victor
de Lima, Thais Martins
de Souza, Heraldo Possolo
Laurindo, Francisco Rafael Martins
Paes, Antonio Marcus de Andrade
Syzygium cumini Leaf Extract Reverts Hypertriglyceridemia via Downregulation of the Hepatic XBP-1s/PDI/MTP Axis in Monosodium L-Glutamate-Induced Obese Rats
title Syzygium cumini Leaf Extract Reverts Hypertriglyceridemia via Downregulation of the Hepatic XBP-1s/PDI/MTP Axis in Monosodium L-Glutamate-Induced Obese Rats
title_full Syzygium cumini Leaf Extract Reverts Hypertriglyceridemia via Downregulation of the Hepatic XBP-1s/PDI/MTP Axis in Monosodium L-Glutamate-Induced Obese Rats
title_fullStr Syzygium cumini Leaf Extract Reverts Hypertriglyceridemia via Downregulation of the Hepatic XBP-1s/PDI/MTP Axis in Monosodium L-Glutamate-Induced Obese Rats
title_full_unstemmed Syzygium cumini Leaf Extract Reverts Hypertriglyceridemia via Downregulation of the Hepatic XBP-1s/PDI/MTP Axis in Monosodium L-Glutamate-Induced Obese Rats
title_short Syzygium cumini Leaf Extract Reverts Hypertriglyceridemia via Downregulation of the Hepatic XBP-1s/PDI/MTP Axis in Monosodium L-Glutamate-Induced Obese Rats
title_sort syzygium cumini leaf extract reverts hypertriglyceridemia via downregulation of the hepatic xbp-1s/pdi/mtp axis in monosodium l-glutamate-induced obese rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446099/
https://www.ncbi.nlm.nih.gov/pubmed/31015892
http://dx.doi.org/10.1155/2019/9417498
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