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Jun-Xu Li

Researcher at University at Buffalo

Publications -  139
Citations -  3422

Jun-Xu Li is an academic researcher from University at Buffalo. The author has contributed to research in topics: Agonist & Imidazoline receptor. The author has an hindex of 30, co-authored 132 publications receiving 2649 citations. Previous affiliations of Jun-Xu Li include Nantong University & Yantai University.

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A review on the pharmacological effects of vitexin and isovitexin.

TL;DR: This review summarized recent findings on various pharmacological activities and associative signalling pathways of vitexin and isoviteXin to provide a reference for future research and clinical applications.
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Gut microbiota from NLRP3-deficient mice ameliorates depressive-like behaviors by regulating astrocyte dysfunction via circHIPK2

TL;DR: This study illustrates the involvement of the Gut microbiota-circHIPK2-astrocyte axis in depression, providing translational evidence that transplantation of the gut microbiota from NLRP3 KO mice may serve as a novel therapeutic strategy for depression.
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Pain and depression comorbidity: a preclinical perspective.

TL;DR: Current preclinical evidence of interactions between pain and depression generally supports the causative relationship of the two conditions and the analysis proposed to apply domain interplay concept in future model development of pain-depression comorbidity and mechanism studies.
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CircDYM ameliorates depressive-like behavior by targeting miR-9 to regulate microglial activation via HSP90 ubiquitination.

TL;DR: It is demonstrated that circular RNA DYM levels were significantly decreased both in the peripheral blood of patients with MDD and in the two depressive-like mouse models: the chronic unpredictable stress (CUS) and lipopolysaccharide (LPS) models, providing translational evidence that circDYM may be a novel therapeutic target for depression.
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Allosteric Modulation: An Alternate Approach Targeting the Cannabinoid CB1 Receptor.

TL;DR: Given the psychoactive effects commonly associated with CB1 receptor agonists and antagonists/inverse agonists, allosteric modulation may offer an alternate approach to attain potential therapeutic benefits while avoiding inherent side effects of orthosteric ligands.