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一氧化氮是否参与5-羟色胺3受体介导的豚鼠近端结肠神经源性舒张?

Is nitric oxide involved in 5-HT3 receptor-mediated neurogenic relaxation of guinea pig proximal colon?

作者信息

Sevcík J, Růzicka V, Slánský J, Smejkal J, Masek K

机构信息

Institute of Pharmacology, Academy of Sciences of the Czech Republic, Prague.

出版信息

Jpn J Pharmacol. 1998 Aug;77(4):265-70. doi: 10.1254/jjp.77.265.

Abstract

The relaxations mediated by the activation of 5-HT receptors in the guinea pig proximal colon were investigated. Longitudinal strips were cut from the colon segment and placed into the bath. In the presence of atropine (0.2 microM), the relaxations were evoked by adding increasing concentrations of 5-HT (1-100 microM). Noncumulative concentration-response curves were established in the absence and presence of either 5-HT or nitric oxide synthase (NOS) antagonists. Selective 5-HT3 antagonists tropisetron (10 and 100 nM) and ondansetron (1 microM) inhibited the relaxations and shifted the concentration-response curves to the right. Similar effects were observed in the presence of the NOS inhibitor N(G)-nitro-L-arginine (3.2, 10, 32 microM) and partly reversed with L-arginine (100, 320 microM). N(G)-nitro-D-arginine, serving as a negative control, was ineffective. The relaxations were further inhibited in the presence of the soluble guanylate cyclase blocker methylene blue (10 microM) or NO scavenger hemoglobin (32 microM). These results suggest that the 5-HT3 receptor plays a role in neurogenic relaxations of guinea pig proximal colon, which are at least partly mediated via release of NO from nerve endings.

摘要

研究了豚鼠近端结肠中5-羟色胺(5-HT)受体激活介导的舒张作用。从结肠段切下纵行肌条并置于浴槽中。在阿托品(0.2微摩尔)存在的情况下,通过添加浓度逐渐增加的5-HT(1-100微摩尔)诱发舒张作用。在不存在和存在5-HT或一氧化氮合酶(NOS)拮抗剂的情况下建立非累积浓度-反应曲线。选择性5-HT3拮抗剂托烷司琼(10和100纳摩尔)和昂丹司琼(1微摩尔)抑制舒张作用并使浓度-反应曲线右移。在NOS抑制剂N(G)-硝基-L-精氨酸(3.2、10、32微摩尔)存在的情况下观察到类似效应,并且L-精氨酸(100、320微摩尔)可部分逆转该效应。作为阴性对照的N(G)-硝基-D-精氨酸无效。在可溶性鸟苷酸环化酶阻滞剂亚甲蓝(10微摩尔)或NO清除剂血红蛋白(32微摩尔)存在的情况下,舒张作用进一步受到抑制。这些结果表明,5-HT3受体在豚鼠近端结肠的神经源性舒张中起作用,这种舒张至少部分是通过神经末梢释放NO介导的。

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