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Jinbao Wei

Researcher at Shanghai Jiao Tong University

Publications -  9
Citations -  136

Jinbao Wei is an academic researcher from Shanghai Jiao Tong University. The author has contributed to research in topics: Neuropathic pain & Visceral pain. The author has an hindex of 4, co-authored 8 publications receiving 70 citations. Previous affiliations of Jinbao Wei include Hubei University of Medicine.

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Effects of regulating intestinal microbiota on anxiety symptoms: A systematic review

TL;DR: More than half of the studies included showed it was positive to treat anxiety symptoms by regulation of intestinal microbiota, and it should be highlighted that the non-probiotic interventions were more effective than the probiotic interventions.
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Involvement of Oxytocin Receptor/Erk/MAPK Signaling in the mPFC in Early Life Stress-Induced Autistic-Like Behaviors.

TL;DR: It is found that juvenile rats subjected to 4 h daily NMS during postnatal days 1 to 20 exhibited autistic-like behavioral deficits without impairments in learning and memory functions and the potential for NMS-driven epigenetic tuning of OXTR expression is suggested.
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Spinal microglial β-endorphin signaling mediates IL-10 and exenatide-induced inhibition of synaptic plasticity in neuropathic pain.

TL;DR: In this article, the authors investigated the regulation of pain hypersensitivity induced by the spinal synaptic transmission mechanisms underlying interleukin (IL)-10 and glucagon-like peptide 1 receptor (GLP-1R) agonist exenatide-induced pain anti-hypersensitivity in neuropathic rats through spinal nerve ligations.
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Bulleyaconitine A Inhibits Visceral Nociception and Spinal Synaptic Plasticity through Stimulation of Microglial Release of Dynorphin A

TL;DR: It is suggested that BAA produces visceral antinociception by stimulating spinal microglial release of dynorphin A, which activates presynaptic κ-opioid receptors in afferent neurons and inhibits spinal synaptic plasticity, highlighting a novel interaction mode between microglia and neurons.
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Synthesis and Biological Evaluation of 4β-N-Acetylamino Substituted Podophyllotoxin Derivatives as Novel Anticancer Agents.

TL;DR: The cytotoxicity test indicated that 12g merits further optimization and development as a new podophyllotoxin-derived lead compound, and the docking studies showed possible interactions between human DNA topoisomerase IIα and 12g.