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六甲基三聚氰胺在肾细胞肿瘤小鼠体内的药代动力学与代谢

Pharmacokinetics and metabolism of hexamethylmelamine in mice bearing renal cell tumors.

作者信息

Dubois J, Atassi G, Hanocq M, Abikhalil F

机构信息

Université Libre de Bruxelles, Institute de Pharmacie Unité de Toxicologie et de chimie bioanalytique, Belgium.

出版信息

Cancer Chemother Pharmacol. 1988;22(4):282-8. doi: 10.1007/BF00254232.

Abstract

The pharmacokinetics of hexamethylmelamine (HMM) and its main metabolites hydroxymethylpentamethylmelamine (HMPMM), pentamethylmelamine (PMM), and 2,2,4,6, tetramethylmelamine (2,2,4,6 TetrMM) were studied in renal cell (RC) tumor tissues and plasma of CDF1 mice that had received IP bolus injections of the maximally tolerated dose (200 mg/kg) of HMM. HMM, PMM, and 2,2,4,6 TetrMM concentrations determined in RC tissues were much higher than the plasma values, as indicated by the pharmacokinetic parameters (Cmax and AUC). On the other hand, very low levels of HMPMM, generally considered to be a potentially active antitumor compound, were detected in the target tissues, whereas this hydroxylated metabolite was stable and easily determined in plasma. High HMM concentrations in RC tissues could correlate with the high sensitivity of the tumor to this drug. However, the behavior of HMPMM remains unclear; related hypotheses are presented in this paper.

摘要

在接受腹腔推注最大耐受剂量(200mg/kg)六甲基三聚氰胺(HMM)的CDF1小鼠的肾细胞(RC)肿瘤组织和血浆中,研究了HMM及其主要代谢产物羟甲基五甲基三聚氰胺(HMPMM)、五甲基三聚氰胺(PMM)和2,2,4,6-四甲基三聚氰胺(2,2,4,6 TetrMM)的药代动力学。如药代动力学参数(Cmax和AUC)所示,在RC组织中测定的HMM、PMM和2,2,4,6 TetrMM浓度远高于血浆值。另一方面,在靶组织中检测到极低水平的HMPMM(通常被认为是一种潜在的活性抗肿瘤化合物),而这种羟基化代谢产物在血浆中稳定且易于测定。RC组织中高浓度的HMM可能与肿瘤对该药物的高敏感性相关。然而,HMPMM的行为仍不清楚;本文提出了相关假说。

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