A PHP Error was encountered

Severity: Warning

Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests

Filename: helpers/my_audit_helper.php

Line Number: 197

Backtrace:

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3145
Function: getPubMedXML

File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global

File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword

File: /var/www/html/index.php
Line: 316
Function: require_once

Phytochemical Analysis of Triphala Extract, In Vitro and In Silico Evaluation of Pancreatic Lipase Inhibition for Obesity Management. | LitMetric

Phytochemical Analysis of Triphala Extract, In Vitro and In Silico Evaluation of Pancreatic Lipase Inhibition for Obesity Management.

Plant Foods Hum Nutr

Department of Food Safety and Analytical Quality Control Laboratory, CSIR-Central Food Technological Research Institute, Mysore, 570020, India.

Published: February 2025

Pancreatic lipase (PL) inhibition is a prominent pharmacological strategy for managing obesity, as it reduces the hydrolysis of dietary triglycerides (TAG) into free fatty acids and monoglycerides. Orlistat, an FDA-approved drug, achieves a 30% reduction in body fat through irreversible covalent inhibition of PL. However, the gastrointestinal side effects limit its long-term use. To address these issues, we explored inhibition using natural compounds from Triphala (TRI), a renowned Ayurvedic formulation comprising three plants - Emblica officinalis (EO), Terminalia bellirica (TB), and Terminalia chebula (TC). This study investigated PL inhibition by an 80% hydro-ethanolic extract of individual herbs (EO, TB, TC) as well as, Triphala (TRI) and its fractions and identified key bioactive compounds - Ellagic acid, Chebulic acid and Corilagin via LC-MS/MS. Qualitative and quantitative phytochemical analyses revealed that TF1 is rich in phenols and tannins and exhibited significant PL inhibition compared to individual herb extracts. Additionally, Ellagic acid, Chebulic acid and Corilagin of TF1 demonstrated notable PL-inhibition, with IC values 58.41 ± 1.92 µg/mL, 125.33 ± 2.80 and 257.81 ± 2.10 µg/mL respectively. Furthermore, the PL inhibition kinetics showed that these bioactives and TRI fractions exhibited mixed inhibition, in contrast to the competitive inhibition of Orlistat (positive control). Molecular docking and 100 ns molecular dynamic simulations of PL-inhibitor complexes revealed that the bioactives bind to key residues in the PL active site. Among the three bioactives, Chebulic acid has better binding energy, primarily due to its substantial electrostatic interactions with the gatekeeper residue D80 of the PL active site. These findings highlight the potential of Triphala bioactives, particularly Chebulic acid and Ellagic acid, to effectively inhibit PL and provide a strategy to manage obesity.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s11130-025-01303-0DOI Listing

Publication Analysis

Top Keywords

chebulic acid
16
ellagic acid
12
inhibition
9
pancreatic lipase
8
lipase inhibition
8
triphala tri
8
tri fractions
8
acid chebulic
8
acid corilagin
8
active site
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!