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: 3165
Function: getPubMedXML

File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global

File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword

File: /var/www/html/index.php
Line: 317
Function: require_once

Astaxanthin Modulates Inflammation in Type 2 Diabetes via Regulation of microRNAs, Lysophosphatidylcholine, and α-Hydroxybutyrate. | LitMetric

Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Astaxanthin is a carotenoid compound that has several beneficial qualities, including antioxidant, anti-inflammatory, antiapoptotic, and antidiabetic effects. This study examined the effects of astaxanthin supplementation on inflammation-related microRNAs, lysophosphatidylcholine, and α-hydroxybutyrate in individuals with Type 2 diabetes. Fifty people with Type 2 diabetes volunteered in a placebo-controlled, randomized, double-blind clinical trial. Subjects were randomly determined to consume either 10 mg of astaxanthin ( = 25) or a placebo ( = 25) for 12 weeks. Quantitative real-time PCR was employed to assess the expression of inflammation-related microRNAs in peripheral blood mononuclear cells both before and after the intervention, and we employed ELISA to ascertain the serum levels of lysophosphatidylcholine and α-hydroxybutyrate. After 12 weeks of supplementation, in comparison with placebo, astaxanthin supplementation resulted in a noteworthy decrease ( < 0.05) in hsa-miR-21, hsa-miR-34a, and hsa-miR-155 expression. In addition, astaxanthin supplementation substantially decreased ( < 0.05) the levels of lysophosphatidylcholine and α-hydroxybutyrate compared with the placebo. These changes suggest that astaxanthin may contribute to the modulation of inflammatory processes and the enhancement of metabolic homeostasis. Moreover, relative to the placebo, astaxanthin supplementation considerably diminished serum plasma glucose, HbA1c, lipid profile, and albumin-to-creatinine ratio levels. In conclusion, the current investigation indicates that astaxanthin supplementation at a dosage of 10 mg per day might be a useful strategy for ameliorating inflammation-related diabetic complications and insulin resistance in Type 2 diabetes patients. Considering the potential role of microRNAs in regulating inflammation and metabolic dysfunction in Type 2 diabetes, these findings suggest that astaxanthin supplementation may modulate inflammation-related microRNAs and metabolic markers, potentially contributing to the management of inflammatory processes and metabolic dysregulation in Type 2 diabetes. Iranian Registry of Clinical Trials (IRCT): IRCT20190305042939N1.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12390588PMC
http://dx.doi.org/10.1155/ije/5878361DOI Listing

Publication Analysis

Top Keywords

type diabetes
24
astaxanthin supplementation
24
lysophosphatidylcholine α-hydroxybutyrate
16
inflammation-related micrornas
12
astaxanthin
10
micrornas lysophosphatidylcholine
8
levels lysophosphatidylcholine
8
placebo astaxanthin
8
inflammatory processes
8
supplementation
7

Similar Publications