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兔肾基底外侧膜囊泡中的有机阴离子转运

Organic anion transport in rabbit renal basolateral membrane vesicles.

作者信息

Makhuli M J, Polkowski C A, Grassl S M

机构信息

Department of Pharmacology, State University of New York, Health Science Center at Syracuse, New York, USA.

出版信息

J Pharmacol Exp Ther. 1995 Apr;273(1):146-53.

PMID:7714760
Abstract

Pathways for p-aminohippurate (PAH) transport across the basolateral membrane of rabbit proximal tubule cells were investigated from studies of [3H] PAH uptake in membrane vesicles isolated by Percoll-density gradient centrifugation. The 10-s uptake of PAH was not significantly different when measured in the absence of cation gradients or in the presence of inwardly directed Na, Li, K or choline gradients that suggests the absence of a mechanism mediating Na-PAH cotransport. A probenicid-sensitive, trans-stimulation of [3H] PAH uptake was observed in the presence of an outward PAH gradient. PAH gradient-driven [3H] PAH uptake was cis-inhibited by glutarate, alpha-ketoglutarate, adipate and sebacate and outward gradients of alpha-ketoglutarate trans-stimulated probenicid-sensitive PAH uptake. A concentrative accumulation of PAH was measured in the presence of an inward Na gradient and the dicarboxylates glutarate or alpha-ketoglutarate. Compared to the absence of a pH gradient, an inside alkaline pH gradient induced an increased PAH uptake both in the presence and absence of CO2/HCO3. Inside-negative and inside-positive voltage differences were observed to stimulate and inhibit alpha-ketoglutarate gradient-driven PAH uptake, respectively. alpha-Ketoglutarate gradient-driven PAH uptake was progressively reduced in the presence of increasing penicillin concentration and an outward gradient of alpha-ketoglutarate induced an increased level of [14C] penicillin uptake. These results suggest the presence of a probenicid-sensitive organic anion exchange mechanism as a pathway for PAH and penicillin transport across the basolateral membrane of rabbit proximal tubule cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过对经Percoll密度梯度离心分离的膜囊泡中[3H]对氨基马尿酸(PAH)摄取的研究,探讨了PAH跨兔近端小管细胞基底外侧膜的转运途径。在不存在阳离子梯度或存在内向的Na、Li、K或胆碱梯度的情况下测量PAH的10秒摄取量,结果无显著差异,这表明不存在介导Na-PAH共转运的机制。在存在外向PAH梯度的情况下,观察到丙磺舒敏感的[3H]PAH摄取的反式刺激。PAH梯度驱动的[3H]PAH摄取被戊二酸、α-酮戊二酸、己二酸和癸二酸顺式抑制,α-酮戊二酸的外向梯度反式刺激丙磺舒敏感的PAH摄取。在存在内向Na梯度以及戊二酸或α-酮戊二酸二羧酸盐的情况下,测量到PAH的浓缩积累。与不存在pH梯度相比,在内侧碱性pH梯度下,无论有无CO2/HCO3,PAH摄取均增加。观察到内侧负电压差和内侧正电压差分别刺激和抑制α-酮戊二酸梯度驱动的PAH摄取。在青霉素浓度增加的情况下,α-酮戊二酸梯度驱动的PAH摄取逐渐减少,α-酮戊二酸的外向梯度导致[14C]青霉素摄取水平增加。这些结果表明存在一种丙磺舒敏感的有机阴离子交换机制,作为PAH和青霉素跨兔近端小管细胞基底外侧膜转运的途径。(摘要截短于250字)

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