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体外囊性纤维化患者与对照者汗液分泌盘腔电位差的差异

Differing luminal potential difference of cystic fibrosis and control sweat secretory coils in vitro.

作者信息

Sato K

出版信息

Am J Physiol. 1984 Oct;247(4 Pt 2):R646-9. doi: 10.1152/ajpregu.1984.247.4.R646.

DOI:10.1152/ajpregu.1984.247.4.R646
PMID:6496713
Abstract

Transepithelial potential difference (PD) of isolated segments of the secretory coil of both human control and cystic fibrosis (CF) eccrine sweat glands was measured during stimulation with methacholine (MCh) and isoproterenol (ISO) in vitro. Negative luminal PD of about 10 and 16 mV developed across the secretory coil epithelium in control and CF secretory coil, respectively, during maximal MCh stimulation. ISO (10(-5) M) stimulation generated a mean of 1.9-mV negative luminal PD in control glands; however, ISO failed to enhance the luminal PD beyond the resting level of 0.9 mV in the CF secretory coil. The inhibition of ISO-induced (10(-5) M) luminal PD in control secretory coil by propranolol (5 X 10(-5) M) but not by atropine (10(-5) M) indicated its pharmacologic specificity. The possibility is discussed that this lack of electrical driving force during ISO stimulation could be one of the mechanisms for the absence of sweating response to beta-adrenergic stimulation in CF sweat glands reported recently (8). The mechanism for the higher MCh-induced luminal PD in the CF secretory coil remains to be studied.

摘要

在体外使用乙酰甲胆碱(MCh)和异丙肾上腺素(ISO)刺激时,测量了人类对照和囊性纤维化(CF)外分泌汗腺分泌盘孤立节段的跨上皮电位差(PD)。在最大MCh刺激期间,对照和CF分泌盘的分泌盘上皮细胞分别产生了约10 mV和16 mV的负腔内PD。ISO(10⁻⁵ M)刺激在对照腺体中产生了平均1.9 mV的负腔内PD;然而,ISO未能使CF分泌盘的腔内PD超过静息水平0.9 mV。普萘洛尔(5×10⁻⁵ M)而非阿托品(10⁻⁵ M)对对照分泌盘中ISO诱导(10⁻⁵ M)的腔内PD的抑制表明了其药理特异性。讨论了ISO刺激期间缺乏电驱动力可能是最近报道的CF汗腺对β-肾上腺素能刺激无出汗反应的机制之一(8)。CF分泌盘中MCh诱导的较高腔内PD的机制仍有待研究。

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引用本文的文献

1
Culture of sweat gland epithelial cells from normal individuals and patients with cystic fibrosis.来自正常个体和囊性纤维化患者的汗腺上皮细胞培养。
In Vitro Cell Dev Biol. 1985 Oct;21(10):597-602. doi: 10.1007/BF02620892.
2
Abnormal apical cell membrane in cystic fibrosis respiratory epithelium. An in vitro electrophysiologic analysis.囊性纤维化呼吸道上皮细胞顶端细胞膜异常。一项体外电生理分析。
J Clin Invest. 1987 Jan;79(1):80-5. doi: 10.1172/JCI112812.
3
Pathophysiology of the exocrine pancreas in cystic fibrosis.囊性纤维化中外分泌胰腺的病理生理学
J R Soc Med. 1989;82 Suppl 16(Suppl 16):2-10.
4
Water secretion and embryological layers in cystic fibrosis.囊性纤维化中的水分泌与胚胎层
J R Coll Physicians Lond. 1990 Apr;24(2):98-100.
5
Antisense oligodeoxynucleotide to the cystic fibrosis gene inhibits anion transport in normal cultured sweat duct cells.针对囊性纤维化基因的反义寡脱氧核苷酸可抑制正常培养的汗腺导管细胞中的阴离子转运。
Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7759-62. doi: 10.1073/pnas.88.17.7759.
6
A1 adenosine-receptor antagonists activate chloride efflux from cystic fibrosis cells.A1 腺苷受体拮抗剂可激活囊性纤维化细胞中的氯离子外流。
Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5562-6. doi: 10.1073/pnas.89.12.5562.