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November 19, 2022NutrientsOpen Access

EEI supplementation significantly attenuated body and liver weight gain, glucose intolerance, and insulin resistance, while improving liver function and modulating gene expression related to insulin signaling, inflammation, and lipid metabolism.

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Why the study?

Interruptins A and B exhibit anti-diabetic, anti-inflammatory, and anti-oxidative effects, but the therapeutic ability and mechanisms of an interruptin-enriched Cyclosorus terminans extract in obese rats remained to be investigated.

Does extract enriched by interruptins A and B (EEI) from Cyclosorus terminans improve insulin resistance and NAFLD in HFD-induced obese rats?

Population

High-fat diet-induced obese rats

Comparison

Extract enriched by interruptins A and B (EEI) treatment

Design

Animal study

Follow-up

2 weeks

Authors

SSSujinda SongtraiWPWasana PratchayasakulBABusarin Arunsak

Discussion

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Overview

Hypothesis-generating for interruptins in obesity-related metabolic disease; prospective human studies needed before clinical adoption.

Structured PICO

Does extract enriched by interruptins A and B (EEI) from Cyclosorus terminans improve insulin resistance and NAFLD in HFD-induced obese rats?

P
Population
High-fat diet (HFD)-induced obese rats
I
Intervention
Extract enriched by interruptins A and B (EEI) from Cyclosorus terminans for 2 weeks
C
Comparator
null
O
Outcome
Insulin resistance and non-alcoholic fatty liver disease (NAFLD) parameters (body and liver weight gain, glucose intolerance, insulin resistance, liver function)surrogate

Extract enriched by interruptins A and B from Cyclosorus terminans ameliorates HFD-induced insulin resistance and NAFLD in rats by modulating insulin signaling, inflammation, and lipid metabolism pathways.

Cite This Study

Songtrai et al. (2022) studied this question.

synapsesocial.com/papers/6a70f0bea528af2d65c3d2eehttps://doi.org/10.3390/nu14224895
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