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大鼠肝细胞质膜中乳酸转运体的证据。

Evidence for a lactate transporter in the plasma membrane of the rat hepatocyte.

作者信息

Monson J P, Smith J A, Cohen R D, Iles R A

出版信息

Clin Sci (Lond). 1982 Apr;62(4):411-20. doi: 10.1042/cs0620411.

Abstract
  1. The rate of uptake in 15 s of L- and D-lactate was studied in isolated hepatocyte preparations from starved rats. 2. Observations were also made of the effect of different concentrations of unlabelled L- and D-lactate on L-[14C]- and D-[14C]-lactate uptake. 3. Lactate uptake into hepatocytes appears to occur by two processes, one saturable and at least partially stereospecific, the other non-saturable, at least up to 28 mmol/l, and probably representing simple non-carrier assisted diffusion. 4. The 15 s uptake of lactate is inhibited by alpha-cyano-3-hydroxycinnamate and by rho-chloromercuriphenylsulphonate but not by the general anion transporter inhibitor 4-acetamido-4'-isothiocyanostilbene-2,2'-disulphonic acid, ouabain or the structural analogue DL-rho-hydroxyphenyl-lactate. 5. Transporter-mediated lactate entry into liver cells is enhanced by lowered extracellular pH. 6. It is suggested that the contribution of the diffusion component of lactate entry into the cell may be exaggerated by the artifactual nature of the isolated hepatocyte preparation, and that under some circumstances in vivo, lactate transport into hepatocytes could determine the rate of lactate removal from blood.
摘要
  1. 研究了饥饿大鼠分离肝细胞制剂中L-乳酸和D-乳酸在15秒内的摄取率。2. 还观察了不同浓度未标记的L-乳酸和D-乳酸对L-[14C]-乳酸和D-[14C]-乳酸摄取的影响。3. 乳酸进入肝细胞似乎通过两个过程发生,一个是可饱和的且至少部分具有立体特异性,另一个是不饱和的,至少在28 mmol/L以下,可能代表简单的非载体协助扩散。4. 乳酸的15秒摄取受到α-氰基-3-羟基肉桂酸酯和对氯汞苯磺酸盐的抑制,但不受一般阴离子转运体抑制剂4-乙酰氨基-4'-异硫氰基芪-2,2'-二磺酸、哇巴因或结构类似物DL-对羟基苯基乳酸的抑制。5. 细胞外pH降低会增强转运体介导的乳酸进入肝细胞的过程。6. 有人提出,乳酸进入细胞的扩散成分的贡献可能因分离肝细胞制剂的人为性质而被夸大,并且在体内某些情况下,乳酸向肝细胞的转运可能决定乳酸从血液中清除的速率。

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