Betahistine co-treatment ameliorates dyslipidemia induced by chronic olanzapine treatment in rats through modulation of hepatic AMPKα-SREBP-1 and PPARα-dependent pathways-Reference-Cited by-同舟云学术

Betahistine co-treatment ameliorates dyslipidemia induced by chronic olanzapine treatment in rats through modulation of hepatic AMPKα-SREBP-1 and PPARα-dependent pathways

Published:2015-10 Issue: Volume:100 Page:36-46
ISSN:1043-6618
Container-title:Pharmacological Research
language:en
Short-container-title:Pharmacological Research

Author:

Liu Xuemei,Lian Jiamei,Hu Chang-Hua,Deng Chao

Funder

Australian National Health and Medical Research Council

Publisher

Elsevier BV

Subject

Pharmacology

Reference70 articles.

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1. PCSK9 dysregulates cholesterol homeostasis and triglyceride metabolism in olanzapine‐induced hepatic steatosis via both receptor‐dependent and receptor‐independent pathways;The FASEB Journal;2024-02-15

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3. Activation of the PERK-CHOP signaling pathway during endoplasmic reticulum stress contributes to olanzapine-induced dyslipidemia;Acta Pharmacologica Sinica;2023-10-25

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5. Epigenetic Histone Methylation of PPARγ and CPT1A Signaling Contributes to Betahistine Preventing Olanzapine-Induced Dyslipidemia;International Journal of Molecular Sciences;2023-05-23