The gut–kidney axis is regulated by astragaloside IV to inhibit cyclosporine A-induced nephrotoxicity

AS-IV improved CICN through the coexpression of the gut-transcriptome-metabolome network. The six pathways related to energy metabolism driven by <i>L. reuteri</i>, including the <i>citrate cycle</i>, <i>ascorbate and alderate metabolism</i>, <i>proximal tube bicarbonate metabolism</i>, <i>glycolysis/gluconeogenesis, ferroptosis, drug metabolism-cytochrome P450</i>, are important mechanisms.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2025-01-27
DOI
https://doi.org/10.3389/fphar.2025.1518481
Citations
8
Primary Topic
Metabolism and Genetic Disorders
Type
article
Field-Weighted Citation Impact
10.55

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article

The gut–kidney axis is regulated by astragaloside IV to inhibit cyclosporine A-induced nephrotoxicity

Le Zhou, Ranran Gao, Cong Han, Wei Li
8 citations
Frontiers in Pharmacology
Metabolism and Genetic Disorders
10.55
article

The gut–kidney axis is regulated by astragaloside IV to inhibit cyclosporine A-induced nephrotoxicity

Le Zhou, Ranran Gao, Cong Han, Wei Li
article en
8 citations

Abstract

AS-IV improved CICN through the coexpression of the gut-transcriptome-metabolome network. The six pathways related to energy metabolism driven by <i>L. reuteri</i>, including the <i>citrate cycle</i>, <i>ascorbate and alderate metabolism</i>, <i>proximal tube bicarbonate metabolism</i>, <i>glycolysis/gluconeogenesis, ferroptosis, drug metabolism-cytochrome P450</i>, are important mechanisms.

Frontiers in PharmacologyVol. 16
Shandong University of Traditional Chinese Medicine (CN), Affiliated Hospital of Shandong University of Traditional Chinese Medicine (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation
Openalex Percentile: Top 2%
Metabolism and Genetic Disorders
10.55
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