Guoshen Cao

ORCID: 0009-0007-7378-6306
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Adipose Tissue and Metabolism
  • Mitochondrial Function and Pathology
  • Plant biochemistry and biosynthesis
  • Lipoproteins and Cardiovascular Health
  • RNA modifications and cancer
  • Coenzyme Q10 studies and effects
  • Diabetes Treatment and Management
  • Cancer, Hypoxia, and Metabolism
  • Peroxisome Proliferator-Activated Receptors
  • Pancreatic function and diabetes
  • ATP Synthase and ATPases Research
  • Diet and metabolism studies
  • Birth, Development, and Health
  • Diabetes Management and Research
  • Muscle metabolism and nutrition
  • Platelet Disorders and Treatments
  • Computational Drug Discovery Methods
  • Renal and related cancers
  • Cell Adhesion Molecules Research

University of Utah
2022-2024

China Pharmaceutical University
2016-2017

State Key Laboratory of Natural Medicine
2016-2017

Carbohydrates and lipids provide the majority of substrates to fuel mitochondrial oxidative phosphorylation. Metabolic inflexibility, defined as an impaired ability switch between these fuels, is implicated in a number metabolic diseases. Here, we explore mechanism by which physical inactivity promotes inflexibility skeletal muscle. We developed mouse model sedentariness, small cage (SMC), that, unlike other classic models disuse mice, faithfully recapitulated responses that occur humans....

10.1172/jci167371 article EN cc-by Journal of Clinical Investigation 2024-04-23

The free fatty acid receptor 1 (FFA1) plays a key role in amplifying glucose-stimulated insulin secretion pancreatic β-cells.

10.1039/c6ra07356e article EN RSC Advances 2016-01-01

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a progressive disorder marked by lipid accumulation, leading to steatohepatitis (MASH). A key feature of the transition MASH involves oxidative stress resulting from defects in mitochondrial phosphorylation (OXPHOS). Here, we show that pathological alterations composition inner membrane (IMM) directly instigate electron transfer inefficiency promote stress. Specifically, cardiolipin (CL) was downregulated with MASLD/MASH...

10.1101/2024.10.10.617517 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-10-10

Intro: Alport Syndrome (AS) is a rare hereditary disorder characterized by progressive renal impairment and sensorineural hearing loss, resulting from mutations in the genes that encode COL4 synthesis. X-linked (XLAS) most common form of AS, comprising an estimated 80% all human AS cases (the others being various forms autosomal recessive or dominant AS), caused on COL4A5 gene. However, to date, there are no animal models XLAS. Methods: To facilitate comprehensive preclinical investigations...

10.1152/physiol.2024.39.s1.1956 article EN Physiology 2024-05-01

Abstract Carbohydrates and lipids provide the majority of substrates to fuel mitochondrial oxidative phosphorylation (OXPHOS). Metabolic inflexibility, defined as an impaired ability switch between these fuels, is implicated in a number metabolic diseases. Here we explore mechanism by which physical inactivity promotes inflexibility skeletal muscle. We developed mouse model sedentariness small cage (SMC) that, unlike other classic models disuse mice, faithfully recapitulates responses that...

10.1101/2022.11.01.514767 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-11-02
Coming Soon ...