Fang Zheng
Professor
University of Arkansas for Medical Sciences
faculty
Pharmacology & Toxicology, College of Medicine
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Biography and Research Information
OverviewAI-generated summary
Fang Zheng, Professor in Pharmacology & Toxicology at the University of Arkansas for Medical Sciences, studies the mechanisms of neurological disorders and the impact of various compounds on the central nervous system. His research is supported by a $335,471 NIH/National Institute of Neurological Disorders and Stroke grant focused on the role of the endothelial NPYR1-TRPC3-ET1 signaling axis in neurovascular coupling dysfunction. Zheng's work investigates the involvement of ion channels, such as Transient Receptor Potential Canonical (TRPC) channels, in conditions like depression and epilepsy. This includes examining how these channels contribute to hyperexcitability and neuronal cell death in the hippocampus, and the pharmacological differences between various TRPC channel subtypes.
His recent publications explore the effects of venlafaxine on gut microbiota in a mouse model of depression, the self-assembly and stability of Vitamin D3 mediated peptides, and the role of pericyte depolarization in brain capillaries. Zheng also investigates the effects of synthetic cannabinoid receptor agonists on electroencephalographic seizures. With an h-index of 23 and over 2,400 citations across 63 publications, his research network includes collaborators such as Kevin D. Phelan and U Thaung Shwe from the University of Arkansas for Medical Sciences.
Metrics
- h-index: 23
- Publications: 63
- Citations: 2,446
Selected Publications
- Increased luminal pressure in brain capillaries drives TRPC3-dependent depolarization and constriction of transitional pericytes (2025) DOI
- Investigating Contributions of Canonical Transient Receptor Potential Channel 3 to Hippocampal Hyperexcitability and Seizure-Induced Neuronal Cell Death (2024) DOI
- Increased Susceptibility to Pilocarpine-Induced Status Epilepticus and Reduced Latency in TRPC1/4 Double Knockout Mice (2023) DOI
- Pharmacological Differences between Native Homomeric Transient Receptor Potential Canonical Type 4 Channels and Heteromeric Transient Receptor Potential Canonical Type 1/4 Channels in Lateral Septal Neurons (2023) DOI
- Canonical Transient Receptor Potential Channel 3 Contributes to Cerebral Blood Flow Changes Associated with Cortical Spreading Depression in Mice (2023) DOI
- Convulsant doses of abused synthetic cannabinoid receptor agonists AB-PINACA, 5F-AB-PINACA, 5F-ADB-PINACA and JWH-018 do not elicit electroencephalographic (EEG) seizures in male mice (2022) DOI
- Canonical Transient Receptor Potential Channels as Novel Targets for Antiepileptic Drugs (2022) DOI
Federal Grants 1 $335,471 total
The Role of the Endothelial NPYR1-TRPC3-ET1 Signaling Axis in Neurovascular Coupling Dysfunction
Research Interests
I have a long-standing interest in the pathophysiology of epilepsy and stroke. Initially trained as a channel biophysicist, I have also acquired experience and knowledge in molecular biology, biochemistry and pharmacology over the years. This allows me to adopt a multidisciplinary approach in my research. I have a equally long-standing interest in the functional roles of metabotropic glutamate receptor (mGluR), and this interest has led to my recent focus on transient receptor potential (TRPC) channels for the last 6 years. We have demonstrated the unique roles of various TRPC family members in seizure and excitotoxicity.
Grants & Funding
- The role of TRPC3 channels in neurovascular coupling and peri-infarct depression UAMS College of Medicine Principal Investigator
- The role of TRPC3 channels in periinfarct depression and stroke UAMS Stroke - Foundation Principal Investigator
- The Role of Endothelial TRPC3 Channels in Neurovascular Coupling NIH Principal Investigator
- The role of TRPC3 channels in neurovascular coupling and peri-infarct depression UAMS College of Medicine Principal Investigator
- ZINC-DEPENDENT APPARENT DESENSITIZATION OF NMDA RECEPTOR NIH Principal Investigator
- Neuroscience Research Center Core Facility at UAMS NIH Co-Investigator
- The role of the endothelial NPYR1-TRPC3-ET1 signaling axis in neurovascular coupling dysfunction NIH Principal Investigator
- MODULATION OF NMDA RECEPTORS BY TYROSINE KINASES NIH Principal Investigator
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