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吡哆醇对大鼠体内2-乙酰-4(5)-四羟基丁基咪唑的处置及淋巴细胞减少效应的影响

Effect of pyridoxine on the disposition and lymphopenic effects of 2-acetyl-4(5)-tetrahydroxybutyl imidazole in the rat.

作者信息

Phillips J A, Paine A J

机构信息

DHSS Department of Toxicology, St Bartholomew's Hospital Medical College, London, UK.

出版信息

Xenobiotica. 1990 Jun;20(6):555-62. doi: 10.3109/00498259009046870.

Abstract
  1. 2-Acetyl-4(5)-tetrahydroxybutyl imidazole (THI) administered orally to rats markedly decreased the peripheral blood lymphocyte count within 16-24 h. The lymphopenic effect of THI was prevented by co-administration of pyridoxine. 2. 14C-THI, administered orally, was absorbed in a dose-dependent manner and excreted unmetabolized. These processes were not affected by co-administration of pyridoxine. 3. In contrast, the rate of excretion of 14C-THI administered i.v. was increased by both dietary and parenterally-administered pyridoxine, and pyridoxine decreased the amount of radiolabel associated with lymphoid tissues. 4. The results show that the lymphopenic effect of THI is not sustained once it is excreted, and indicate that pyridoxine and THI may compete for the same binding site in lymphoid tissues.
摘要
  1. 给大鼠口服2-乙酰-4(5)-四羟基丁基咪唑(THI)可在16 - 24小时内显著降低外周血淋巴细胞计数。同时给予吡哆醇可预防THI的淋巴细胞减少作用。2. 口服给予的14C-THI呈剂量依赖性吸收且未代谢排泄。这些过程不受同时给予吡哆醇的影响。3. 相比之下,静脉注射14C-THI的排泄速率因膳食和胃肠外给予的吡哆醇而增加,且吡哆醇减少了与淋巴组织相关的放射性标记量。4. 结果表明,THI一旦排泄,其淋巴细胞减少作用就不会持续,并表明吡哆醇和THI可能在淋巴组织中竞争相同的结合位点。

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