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儿茶酚胺降低豚鼠内淋巴囊的直流电位。

Catecholamines depress endolymphatic sac direct current potential in guinea pigs.

作者信息

Mori N, Uozumi N, Sakai S

机构信息

Department of Otolaryngology, Kagawa Medical School, Japan.

出版信息

Am J Physiol. 1990 Nov;259(5 Pt 2):R921-4. doi: 10.1152/ajpregu.1990.259.5.R921.

Abstract

To test the possibility that catecholamines have an influence on the function of the endolymphatic sac (ES), which is known to absorb the endolymph, the effect of catecholamines on the ES direct current potential (ESP) was examined in the guinea pig. The ESP was recorded extradurally by the posterior occipital approach. Isoproterenol (Iso), epinephrine (Epi), and norepinephrine (NE) were administered intravenously for 4 min using an infusion pump. Catecholamines reversibly depressed the ESP with the rank order of potency Iso greater than Epi greater than NE. The threshold doses were 0.021, 0.27, and 1.94 micrograms/kg for Iso, Epi, and NE, respectively. beta-Antagonist (propranolol) blocked the action of catecholamines on the ESP but alpha-antagonist (phentolamine) did not. This indicates that beta-adrenergic action induces the ESP change. This study implies that catecholamines may regulate the function of the ES.

摘要

为了验证儿茶酚胺对已知具有吸收内淋巴功能的内淋巴囊(ES)功能有影响这一可能性,研究了儿茶酚胺对豚鼠内淋巴囊直流电位(ESP)的作用。通过枕后入路在硬膜外记录ESP。使用输液泵静脉注射异丙肾上腺素(Iso)、肾上腺素(Epi)和去甲肾上腺素(NE)4分钟。儿茶酚胺以Iso>Epi>NE的效力顺序可逆性地降低ESP。Iso、Epi和NE的阈剂量分别为0.021、0.27和1.94微克/千克。β拮抗剂(普萘洛尔)可阻断儿茶酚胺对ESP的作用,但α拮抗剂(酚妥拉明)则不能。这表明β肾上腺素能作用可诱导ESP变化。本研究提示儿茶酚胺可能调节内淋巴囊的功能。

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