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尼古丁及其代谢物可替宁在大鼠体内的分布与滞留随时间的变化情况。

Distribution and retention of nicotine and its metabolite, cotinine, in the rat as a function of time.

作者信息

Sastry B V, Chance M B, Singh G, Horn J L, Janson V E

机构信息

Department of Pharmacology, University School of Medicine, Nashville, Tenn., USA.

出版信息

Pharmacology. 1995 Feb;50(2):128-36. doi: 10.1159/000139274.

Abstract

Nicotine is oxidized to its major metabolite, cotinine, which has a long biological half-life (19-24 h). The plasma concentration of cotinine has been used as an index of tobacco smoke exposure. Cotinine possibly increases the turnover rate of platelet-activating factor (PAF) because it is a potent activator of PAF hydrolase, and it may play a significant role in tobacco-induced arterial thrombosis. Therefore, we studied the distribution and retention of nicotine as it was metabolized to cotinine in the rat. Nicotine (1 mg/kg, 5 microCi/kg) was administered into the femoral vein of male Sprague-Dawley rats under nembutal anesthesia. At different times (5-60 min) after nicotine administration, nicotine and its metabolite, cotinine, were determined by HPLC in plasma, liver, kidney, heart and brain. Within 5-10 min after administration, nicotine concentrations reached peak values in plasma (2,160 pmol/ml) and the organs analyzed. The plasma level of nicotine decreased by 50% within 20 min (half-time) after its intravenous administration. The half-time of nicotine in the brain was about 50 min. The half-times of nicotine for the other organs were about 20-25 min. The major metabolite, cotinine, accumulated in plasma, and by about 30 min the concentrations of nicotine and cotinine in plasma were about equal (890-1,000 pmol/ml). While cotinine accumulated in plasma, nicotine was eliminated by the kidney. While the nicotine concentrations decreased with time in all organs, cotinine concentrations remained constant. These observations indicate that nicotine is renally eliminated or metabolized to cotinine while cotinine exhibits a long retention time and accumulates in plasma.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

尼古丁被氧化成其主要代谢产物可替宁,可替宁具有较长的生物半衰期(19 - 24小时)。可替宁的血浆浓度已被用作烟草烟雾暴露的指标。可替宁可能会增加血小板活化因子(PAF)的周转率,因为它是PAF水解酶的有效激活剂,并且它可能在烟草诱导的动脉血栓形成中起重要作用。因此,我们研究了尼古丁在大鼠体内代谢为可替宁时的分布和潴留情况。在戊巴比妥麻醉下,将尼古丁(1毫克/千克,5微居里/千克)注入雄性Sprague-Dawley大鼠的股静脉。在给予尼古丁后的不同时间(5 - 60分钟),通过高效液相色谱法测定血浆、肝脏、肾脏、心脏和大脑中的尼古丁及其代谢产物可替宁。给药后5 - 10分钟内,尼古丁浓度在血浆(2,160皮摩尔/毫升)和所分析的器官中达到峰值。静脉注射后20分钟(半衰期)内,血浆中尼古丁水平下降了50%。尼古丁在大脑中的半衰期约为50分钟。尼古丁在其他器官中的半衰期约为20 - 25分钟。主要代谢产物可替宁在血浆中蓄积,到约30分钟时,血浆中尼古丁和可替宁的浓度大致相等(890 - 1,000皮摩尔/毫升)。当可替宁在血浆中蓄积时,尼古丁通过肾脏被清除。虽然所有器官中的尼古丁浓度随时间下降,但可替宁浓度保持恒定。这些观察结果表明,尼古丁通过肾脏被清除或代谢为可替宁,而可替宁具有较长的潴留时间并在血浆中蓄积。(摘要截断于250字)

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