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2-巯基苯并噻唑和2-巯基苯并噻唑二硫化物在大鼠静脉注射、口服和局部给药以及豚鼠局部给药后的处置情况。

Disposition of 2-mercaptobenzothiazole and 2-mercaptobenzothiazole disulfide in rats dosed intravenously, orally, and topically and in guinea pigs dosed topically.

作者信息

el Dareer S M, Kalin J R, Tillery K F, Hill D L, Barnett J W

机构信息

Southern Research Institute, Birmingham, Alabama 35255-3505.

出版信息

J Toxicol Environ Health. 1989;27(1):65-84. doi: 10.1080/15287398909531279.

Abstract

To determine the metabolic disposition of [14C]-2-mercaptobenzothiazole (MBT) and [14C]-2-mercaptobenzothiazole disulfide (MBTS), male and female rats were dosed topically. Topical doses were 36.1 micrograms/animal for [14C]MBT and 33.6 micrograms/animal for [14C]MBTS. Although more MBT passed through the skin than MBTS and although, relative to rats, guinea pigs absorbed a greater percentage of the dose (33.4% compared to 16.1-17.5% of the MBT and 12.2% compared to 5.94-7.87% for MBTS), the disposition of radioactivity derived from the two compounds was similar. Washing of the skin removed more of the radioactivity from guinea pigs than from rats. For both sexes of rats dosed intravenously with [14C]MBT (0.602 mg/kg) or [14C]MBTS (0.571 mg/kg), disposition of the compounds was similar. In 72 h, 90.9-101% of the dose appeared in the urine and 3.79-15.1% in the feces. At this time, a small portion of the administered radioactivity (1.52-1.96% of the dose) remained associated with erythrocytes. Oral dosing of rats for 14 d with unlabeled MBT (0.510 mg/kg.d) prior to a single dose of [14C]MBT (0.503 mg/kg) or with unlabeled MBTS (0.521 mg/kg.d) prior to a single dose of [14C]MBTS (0.730 mg/kg). For both sexes, disposition of the compounds was similar. At 96 h after dosing, a small portion of the administered radioactivity (1.20-1.69% of the dose) remained associated with erythrocytes, most of which was bound to the membranes. For both compounds and sexes, 60.8-101% of the radioactivity administered appeared in the urine and 3.46-9.99% in the feces in 96 h. At the time, only trace amounts of radioactivity remained in tissues other than blood. Of these tissues, thyroid contained the highest concentration. In the urine, there was a detectable MBT or MBTS, but there were two metabolites, one of which was identified as a thioglucuronide derivative of MBT. The other was possibly a sulfonic acid derivative of MBT. In conclusion, there were similarities in absorption, distribution, and metabolism of [14C]MBT and [14C]MBTS in rats and in guinea pigs, indicating that [14C]MBTS was readily converted to [14C]MBT.

摘要

为了确定[¹⁴C]-2-巯基苯并噻唑(MBT)和[¹⁴C]-2-巯基苯并噻唑二硫化物(MBTS)的代谢情况,对雄性和雌性大鼠进行了局部给药。[¹⁴C]MBT的局部给药剂量为36.1微克/只动物,[¹⁴C]MBTS的局部给药剂量为33.6微克/只动物。尽管通过皮肤的MBT比MBTS多,并且相对于大鼠,豚鼠吸收的剂量百分比更高(MBT为33.4%,而大鼠为16.1 - 17.5%;MBTS为12.2%,而大鼠为5.94 - 7.87%),但两种化合物产生的放射性分布相似。皮肤清洗后,豚鼠皮肤去除的放射性比大鼠更多。对于静脉注射[¹⁴C]MBT(0.602毫克/千克)或[¹⁴C]MBTS(0.571毫克/千克)的雌雄大鼠,两种化合物的分布情况相似。在72小时内,90.9 - 101%的剂量出现在尿液中,3.79 - 15.1%出现在粪便中。此时,一小部分给药的放射性(剂量的1.52 - 1.96%)仍与红细胞相关。在单次注射[¹⁴C]MBT(0.503毫克/千克)之前,对大鼠口服未标记的MBT(0.510毫克/千克·天)14天;或在单次注射[¹⁴C]MBTS(0.730毫克/千克)之前,口服未标记的MBTS(0.521毫克/千克·天)。对于雌雄两性,两种化合物的分布情况相似。给药后96小时,一小部分给药的放射性(剂量的1.20 - 1.69%)仍与红细胞相关,其中大部分与细胞膜结合。对于两种化合物和两性,给药的放射性在96小时内60.8 - 101%出现在尿液中,3.46 - 9.99%出现在粪便中。此时,除血液外的组织中仅残留痕量放射性。在这些组织中,甲状腺中的浓度最高。在尿液中,可检测到MBT或MBTS,但有两种代谢产物,其中一种被鉴定为MBT的硫代葡糖醛酸衍生物。另一种可能是MBT的磺酸衍生物。总之,[¹⁴C]MBT和[¹⁴C]MBTS在大鼠和豚鼠中的吸收、分布和代谢存在相似性,表明[¹⁴C]MBTS易于转化为[¹⁴C]MBT。

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