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组胺H2受体拮抗剂对大鼠肾皮质切片、离体近端小管和远端小管中金刚烷胺摄取的不同影响。

Differential effects of histamine H2 receptor antagonists on amantadine uptake in the rat renal cortical slice, isolated proximal tubule and distal tubule.

作者信息

Wong L T, Smyth D D, Sitar D S

机构信息

Department of Pharmacology & Therapeutics, University of Manitoba, Winnipeg, Canada.

出版信息

J Pharmacol Exp Ther. 1991 Jul 1;258(1):320-4.

PMID:2072304
Abstract

The interaction between amantadine and two histamine receptor antagonists was examined in the rat kidney. Amantadine (10 microM, 30 sec) was actively accumulated by cortical slices (slice/medium ratio = 0.4 +/- 0.3 [3.3 +/- 0.3 at 4 min], mean +/- S.E.M.), isolated proximal tubules (tubule/medium ratio = 35 +/- 1) and distal tubules (tubule/medium ratio = 19 +/- 2). In cortical slices, low cimetidine concentrations facilitated amantadine accumulation, whereas higher concentrations produced inhibition. Uptake in proximal tubules was enhanced by cimetidine and reached a maximum at approximately 100 microM. Cimetidine (20 microM) decreased the apparent Km (88 +/- 5 to 55 +/- 3 microM, P less than .005) without altering Vmax (6.8 +/- 0.5 to 5.8 +/- 0.6 nmol/mg/min). Conversely, cimetidine did not enhance uptake in distal tubules but elicited competitive inhibition at concentrations greater than 1 mM. Although this may partially delineate the differences observed between the cortical slice and proximal tubule data, such a discrepancy may also implicate additional sites of interaction in other segments of the cortical nephron and/or cimetidine inhibition of the relatively more significant luminal amantadine efflux in the proximal tubules. Ranitidine did not enhance amantadine accumulation but produced inhibition at high concentrations. In proximal and distal tubule preparations, ranitidine (10 mM) increased Km from 86 +/- 7 to 121 +/- 8 and 95 +/- 5 to 160 +/- 10 microM, respectively (P less than .05), whereas Vmax was not changed (8.9 +/- 0.7 to 7.9 +/- 0.8 and 4.3 +/- 0.1 to 3.8 +/- 0.2 nmol/mg/min, respectively).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在大鼠肾脏中研究了金刚烷胺与两种组胺受体拮抗剂之间的相互作用。金刚烷胺(10微摩尔,30秒)可被皮质切片(切片/培养基比值 = 0.4 ± 0.3 [4分钟时为3.3 ± 0.3],平均值 ± 标准误)、分离的近端小管(小管/培养基比值 = 35 ± 1)和远端小管(小管/培养基比值 = 19 ± 2)主动摄取。在皮质切片中,低浓度西咪替丁促进金刚烷胺摄取,而高浓度则产生抑制作用。西咪替丁可增强近端小管的摄取,并在约100微摩尔时达到最大值。西咪替丁(20微摩尔)降低了表观米氏常数(从88 ± 5降至55 ± 3微摩尔,P < 0.005),而不改变最大反应速度(从6.8 ± 0.5降至5.8 ± 0.6纳摩尔/毫克/分钟)。相反,西咪替丁不会增强远端小管的摄取,但在浓度大于1毫摩尔时会引发竞争性抑制。尽管这可能部分解释了皮质切片和近端小管数据之间观察到的差异,但这种差异也可能意味着皮质肾单位其他节段存在额外的相互作用位点,和/或西咪替丁抑制了近端小管中相对更显著的管腔金刚烷胺外排。雷尼替丁不会增强金刚烷胺摄取,但在高浓度时会产生抑制作用。在近端和远端小管制剂中,雷尼替丁(10毫摩尔)分别将米氏常数从86 ± 7增加到121 ± 8和从95 ± 5增加到160 ± 10微摩尔(P < 0.05),而最大反应速度未改变(分别从8.9 ± 0.7降至7.9 ± 0.8和从4.3 ± 0.1降至3.8 ± 0.2纳摩尔/毫克/分钟)。(摘要截短于250字)

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