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Nan Zhang

Researcher at Fourth Military Medical University

Publications -  14
Citations -  687

Nan Zhang is an academic researcher from Fourth Military Medical University. The author has contributed to research in topics: Neuroprotection & Receptor. The author has an hindex of 13, co-authored 14 publications receiving 595 citations.

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G-Protein-Coupled Receptor 30 Mediates Rapid Neuroprotective Effects of Estrogen via Depression of NR2B-Containing NMDA Receptors

TL;DR: Findings provide direct evidence that fast neuroprotection by estradiol is partially mediated by GPR30 and the subsequent downregulation of NR2B-containing NMDARs and the modulation of DAPK1 activity by G PR30 may be an important mediator of estradio-dependent neuroprotection.
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Estrogen receptor GPR30 exerts anxiolytic effects by maintaining the balance between GABAergic and glutamatergic transmission in the basolateral amygdala of ovariectomized mice after stress

TL;DR: The results indicate that estradiol reduces anxiety-like behaviors induced by acute stress at least partially through GPR30 signaling, maintaining the balance between GABAergic and glutamatergic transmission in the BLA of OVX-stressed mice.
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Neuroprotective effects of Salidroside and its analogue tyrosol galactoside against focal cerebral ischemia in vivo and H2O2-induced neurotoxicity in vitro.

TL;DR: The neuroprotective effects of these two analogues show that Tyr has a better antioxidative action compared with Sal both in vivo and in vitro, and suggest that the antioxidant activity of Sal and Tyr may be partly due to their different substituents in their glycosyl groups.
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Neuroprotective effects of oestrogen against oxidative toxicity through activation of G-protein-coupled receptor 30 receptor.

TL;DR: The aim of the present study was to investigate the role of G‐protein‐coupled receptor 30 (GPR30), a new kind of oestrogen receptor, in the neuroprotection against oxidative insult.
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Attenuation of Reserpine-Induced Pain/Depression Dyad by Gentiopicroside Through Downregulation of GluN2B Receptors in the Amygdala of Mice

TL;DR: This study provides strong evidence that Gent inhibits reserpine-induced pain/depression dyad by downregulating GluN2B receptors in the amygdala and reverses the changes in the levels of biogenic amines, caspase-3, and Glun2B-containing NMDA receptors in amygdala.