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编 号:F337343
分子式:C21H31N5O2
分子量:385.5
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10mM*1mL in DMSO
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5mg
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10mg
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25mg
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50mg
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100mg
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生物活性:
Buspirone is an orally active 5-HT1A receptor agonist, and a dopamine D2 autoreceptorsant antagonist. Buspirone is an anxiolytic agent, and can be used for the generalized anxiety disorder research.

体内研究:
Buspirone(1-5 mg/kg;腹腔注射和注射;持续 5 天;C57BL/6N 小鼠)可减少焦虑/抑郁行为。Buspirone(1-5 mg/kg;腹腔注射和静脉注射;持续 5 天;C57BL/6N 小鼠)可恢复肠道微生物群固定应力 (IS) 转变的 β 多样性。Animal Model:Male C57BL/6N mice
Dosage:1 and 5 mg/kg
Administration:Oral gavage and intraperitoneal injection; for 5 days
Result:Reduced TNF-α expression and NF-κB+/Iba1+ cell population in the hippocampus and myeloperoxidase activity and NF-κB+/CD11c+ cell population in the colon.
Animal Model:Male C57BL/6N mice
Dosage:1 and 5 mg/kg
Administration:Oral gavage and intraperitoneal injection; for 5 days
Result:Reduced the IS- or Escherichia coli K1 (EC)-induced gut Proteobacteria population.

体外研究:
Buspirone 的抗焦虑和抗抑郁作用是通过分别激活 5-HT1A 自身受体和 5-HT1A 异质受体来产生的。Buspirone(0-400 μg/mL;6 小时)对淋巴细胞具有细胞毒性作用。Buspirone(0-180 μg/mL;0-3 小时;淋巴细胞)诱导 ROS 形成、线粒体膜电位崩溃 (MMP)、脂质过氧化、溶酶体损伤和谷胱甘肽二硫化物 (GSSG) 升高。
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