Muscadine or amla extracts standardized to ellagic acid content ameliorate glucolipotoxicity associated β-cell dysfunction via inhibition of IL-1β and improved insulin secretion

Abstract Glucolipotocixity induces IL-1 β secretion which impairs pancreatic β-cell insulin secretion. Ellagic acid and urolithin A have strong anti-inflammatory effect on cells. Muscadine and amla are very good sources of ellagic acid. The present study examined the effect of ellagic acid, ellagic...

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Main Authors: Srikanth Earpina, Karen McDonough, Millicent Yeboah-Awudzi, Kristina J. Cook, Sita Aggarwal, Jack N. Losso
Format: Article
Language:English
Published: BMC 2020-05-01
Series:Food Production, Processing and Nutrition
Subjects:
Online Access:http://link.springer.com/article/10.1186/s43014-020-00023-z
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author Srikanth Earpina
Karen McDonough
Millicent Yeboah-Awudzi
Kristina J. Cook
Sita Aggarwal
Jack N. Losso
author_facet Srikanth Earpina
Karen McDonough
Millicent Yeboah-Awudzi
Kristina J. Cook
Sita Aggarwal
Jack N. Losso
author_sort Srikanth Earpina
collection DOAJ
description Abstract Glucolipotocixity induces IL-1 β secretion which impairs pancreatic β-cell insulin secretion. Ellagic acid and urolithin A have strong anti-inflammatory effect on cells. Muscadine and amla are very good sources of ellagic acid. The present study examined the effect of ellagic acid, ellagic acid-rich muscadine or amla extract, or urolothin A on inflammation in β cells under glucolipotoxic conditions. Rat NIT-1 β cells were incubated in glucolipotoxic conditions (33.3 mM glucose, 250 μM palmitic acid or 33.3 mM glucose + 250 μM palmitic acid with or without ellagic acid, ellagic acid-rich muscadine or amla extracts standardized to its ellagic acid content, or urolithin A). Inflammatory status was evidenced by ELISA analysis of insulin and IL-1β secretion. Ellagic acid-rich muscadine or amla extracts dose-dependently stimulated insulin secretion and down-regulated IL-1β better than pure ellagic acid, or urolithin A. Urolithin A did not statistically stimulate insulin secretion and did not inhibit IL-1β.
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spelling doaj.art-419e0a0910a0470b9492ec90c89df3dd2022-12-21T18:22:37ZengBMCFood Production, Processing and Nutrition2661-89742020-05-012111110.1186/s43014-020-00023-zMuscadine or amla extracts standardized to ellagic acid content ameliorate glucolipotoxicity associated β-cell dysfunction via inhibition of IL-1β and improved insulin secretionSrikanth Earpina0Karen McDonough1Millicent Yeboah-Awudzi2Kristina J. Cook3Sita Aggarwal4Jack N. Losso5Chronic Degenerative Disease Prevention Laboratory, School of Nutrition and Food Science, Louisiana State University AgCenter, Louisiana State University SystemSchool of Animal Science, Louisiana State University AgCenter, Louisiana State University SystemChronic Degenerative Disease Prevention Laboratory, School of Nutrition and Food Science, Louisiana State University AgCenter, Louisiana State University SystemChronic Degenerative Disease Prevention Laboratory, School of Nutrition and Food Science, Louisiana State University AgCenter, Louisiana State University SystemWilliam Hansel Cancer Prevention, Pennington Biomedical Research Center, Louisiana State University SystemChronic Degenerative Disease Prevention Laboratory, School of Nutrition and Food Science, Louisiana State University AgCenter, Louisiana State University SystemAbstract Glucolipotocixity induces IL-1 β secretion which impairs pancreatic β-cell insulin secretion. Ellagic acid and urolithin A have strong anti-inflammatory effect on cells. Muscadine and amla are very good sources of ellagic acid. The present study examined the effect of ellagic acid, ellagic acid-rich muscadine or amla extract, or urolothin A on inflammation in β cells under glucolipotoxic conditions. Rat NIT-1 β cells were incubated in glucolipotoxic conditions (33.3 mM glucose, 250 μM palmitic acid or 33.3 mM glucose + 250 μM palmitic acid with or without ellagic acid, ellagic acid-rich muscadine or amla extracts standardized to its ellagic acid content, or urolithin A). Inflammatory status was evidenced by ELISA analysis of insulin and IL-1β secretion. Ellagic acid-rich muscadine or amla extracts dose-dependently stimulated insulin secretion and down-regulated IL-1β better than pure ellagic acid, or urolithin A. Urolithin A did not statistically stimulate insulin secretion and did not inhibit IL-1β.http://link.springer.com/article/10.1186/s43014-020-00023-zMuscadineAmlaEllagic acidNIT-1 pancreatic β-cells; glucosePalmitic acidGlucolipotoxicity
spellingShingle Srikanth Earpina
Karen McDonough
Millicent Yeboah-Awudzi
Kristina J. Cook
Sita Aggarwal
Jack N. Losso
Muscadine or amla extracts standardized to ellagic acid content ameliorate glucolipotoxicity associated β-cell dysfunction via inhibition of IL-1β and improved insulin secretion
Food Production, Processing and Nutrition
Muscadine
Amla
Ellagic acid
NIT-1 pancreatic β-cells; glucose
Palmitic acid
Glucolipotoxicity
title Muscadine or amla extracts standardized to ellagic acid content ameliorate glucolipotoxicity associated β-cell dysfunction via inhibition of IL-1β and improved insulin secretion
title_full Muscadine or amla extracts standardized to ellagic acid content ameliorate glucolipotoxicity associated β-cell dysfunction via inhibition of IL-1β and improved insulin secretion
title_fullStr Muscadine or amla extracts standardized to ellagic acid content ameliorate glucolipotoxicity associated β-cell dysfunction via inhibition of IL-1β and improved insulin secretion
title_full_unstemmed Muscadine or amla extracts standardized to ellagic acid content ameliorate glucolipotoxicity associated β-cell dysfunction via inhibition of IL-1β and improved insulin secretion
title_short Muscadine or amla extracts standardized to ellagic acid content ameliorate glucolipotoxicity associated β-cell dysfunction via inhibition of IL-1β and improved insulin secretion
title_sort muscadine or amla extracts standardized to ellagic acid content ameliorate glucolipotoxicity associated β cell dysfunction via inhibition of il 1β and improved insulin secretion
topic Muscadine
Amla
Ellagic acid
NIT-1 pancreatic β-cells; glucose
Palmitic acid
Glucolipotoxicity
url http://link.springer.com/article/10.1186/s43014-020-00023-z
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