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体外研究肾上腺素能受体激动剂对大鼠十二指肠肠嗜铬细胞5-羟色胺释放的影响。

The release of serotonin from rat duodenal enterochromaffin cells by adrenoceptor agonists studied in vitro.

作者信息

Pettersson G, Dahlström A, Larsson I, Lundberg J M, Ahlman H, Kewenter J

出版信息

Acta Physiol Scand. 1978 Jun;103(2):219-24. doi: 10.1111/j.1748-1716.1978.tb06209.x.

Abstract

The serotonin (5-HT) content of enterochromaffin cells (EC) was studied by a cytofluorimetric method in biopsies from rat duodenal mucosa after in vitro incubation with different adrenoceptor agonists and antagonists and acetylcholine (ACh). Noradrenaline (NA), Adrenaline (A) and Isoprenaline (IP) caused a decrease of 5-HT in EC down to 40--60% and for NA and A this effect was concentration-dependent. The effect was antagonized by d,1-propranolol but not by d-propranolol, metoprolol, phentolamine or phenoxybenzamine indicating that the 5-HT release from EC is probably mediated via a true beta-adrenoceptor mechanism possibly of the beta2 type. ACh also decreased the 5-HT content of EC but was much less potent than the adrenergic substances. Dopamine (DA) had no effect.

摘要

采用细胞荧光测定法,研究了大鼠十二指肠黏膜活检组织中肠嗜铬细胞(EC)的5-羟色胺(5-HT)含量。这些活检组织在体外分别与不同的肾上腺素能受体激动剂、拮抗剂以及乙酰胆碱(ACh)共同孵育。去甲肾上腺素(NA)、肾上腺素(A)和异丙肾上腺素(IP)可使EC中的5-HT含量降低至40%-60%,并且NA和A的这种作用呈浓度依赖性。该作用可被消旋普萘洛尔拮抗,但不能被右旋普萘洛尔、美托洛尔、酚妥拉明或酚苄明拮抗,这表明EC释放5-HT可能是通过一种真正的β-肾上腺素能受体机制介导的,可能为β2型。ACh也可降低EC中的5-HT含量,但其作用强度远低于肾上腺素能物质。多巴胺(DA)则无此作用。

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