异丙肾上腺素和利尿加压素对蟾蜍膀胱渗透性的影响。

C Lippe, C Ardizzone
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引用次数: 1

摘要

异丙肾上腺素是一种β肾上腺素能激动剂,可显著增加蟾蜍膀胱内的上皮通量;这种效应与剂量有关,10(-6)M是达到最大作用所必需的。这种作用的选择性不如利尿激素:异丙肾上腺素治疗下J尿素/J硫脲的比值为3.8,利尿激素治疗下为30.4。这两种激素对主要脂溶性分子(即安替比林)的渗透性影响不同:加压素增加安替比林的渗透性,而异丙肾上腺素则降低它。此外,焦碳酸二乙酯处理的管腔膜强烈抑制抗利尿素对尿素通透性的影响,而异丙肾上腺素对尿素通透性的影响未加修饰。然而,这两种激素的作用并不是叠加的。这些结果允许我们假设,当膀胱受到特定激素刺激时,组织有一种抑制其他激素作用的反馈机制。
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Permeability properties of the Bufo bufo bladder as affected by isoprenaline and vasopressin.

Isoprenaline, a beta adrenergic agonist, strongly increases both transepithelial fluxes across the urinary bladder of Bufo bufo; this effect is dose dependent, 10(-6)M being necessary for the maximal action. This effect is less selective than that of vasopressin: the ratio J urea/J thiourea is 3.8 under isoprenaline and 30.4 under vasopressin treatment. Both hormones differently affect the permeability of a mainly liposoluble molecule, i.e. antipyrine: vasopressin increases antipyrine permeability, while isoprenaline decreases it. Moreover diethylpyrocarbonate treatment of the luminal membrane strongly inhibits vasopressin effect on urea permeability leaving unmodified that of isoprenaline. However, the actions of both hormones are not additive. These results allows to assume that the tissue has a feedback mechanism which inhibits other hormonal action while the bladder is stimulated by a particular hormone.

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