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茜草科

新虫 (小有名气)

[求助] 为什么要肝门静脉取血 已有4人参与

今天看了一篇代谢组学的文献,研究一方剂对肝的治疗作用,采用肝门静脉取血,
为什么呀?避免首过效应?这样对代谢物有什么影响?
和眼眶、颈动脉相比有什么特点啊
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茜草科

新虫 (小有名气)

引用回帖:
17楼: Originally posted by richbird at 2014-06-19 17:34:23
代谢组学会受吸收药物和药物代谢的双重影响,蛋白组学受到的影响相对较少。因为是复方,化合物成分复杂。但是对于多数药物而言,会结合在血浆蛋白上。当然组织器官也有有一定的蛋白结合,假如没有特异性结合或者分布 ...

把方法的英语原文贴出来吧,避免英语理解错了的原因

Animal sampling and handing
The animals were randomly assigned to 10 groups of 6 rats each as follows: control, HI, YCHT, D, G, R, DG, DR, GR and DGR groups. The rats in the control group were given distilled water for 8 consecutive days and anesthetized via an intraperitoneal injection of 1% pentobarbital sodium (0.15 ml/100 g body weight) on day 9. The rats in the HI group were orally administrated 20% CCL4 (1 ml/kg body weight) for 8 consecutive days (at 6:00 p.m.), and on day 9, the rats were anesthetized as in the control group. Simultaneously, other groups were administrated CCL4 and various treatments for 9 consecutive days, then anesthetized as in the control group. The rats were orally given 1 ml/100 g each, and the doses of the three components used in this study were administered in accordance with the “Shanghanlun”. Blood was collected from the hepatic portal vein, and plasma was separated via centrifugation at 4,500 rpm for 5 min at 4°C, flash frozen in liquid nitrogen and stored at -80°C until the liver function tests and metabolomics and proteomics analyses were performed. The plasma ALT, AST, ALP, GSH-PX and SOD activities and MDA, TG, GT, CHOL, TP, D-BIL and T-BIL contents were measured according to the manufacturer’s instructions. The rat livers were removed immediately after plasma collection and stored at -70°C until analysis. Urine was collected daily (at 6:00 a.m.) from the metabolic cages at ambient temperature throughout the entire procedure and centrifuged at 10,000 rpm at 4°C for 5 min; the supernatants were then stored frozen at -20°C for subsequent metabolomic analysis.
22楼2014-06-19 21:27:10
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bigpalewolf

金虫 (正式写手)

【答案】应助回帖

感谢参与,应助指数 +1
关键给药途径是啥啊,如果口服应该是避免了受过效应。研究肝外代谢。如果尾静脉给药那就没啥意义。
2楼2014-06-12 01:06:55
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茜草科

新虫 (小有名气)

引用回帖:
2楼: Originally posted by bigpalewolf at 2014-06-12 01:06:55
关键给药途径是啥啊,如果口服应该是避免了受过效应。研究肝外代谢。如果尾静脉给药那就没啥意义。

谢谢!
是口服 为什么要研究肝外代谢呢 这个不是研究药物对肝的治疗作用

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3楼2014-06-12 07:18:36
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bigpalewolf

金虫 (正式写手)

引用回帖:
3楼: Originally posted by 茜草科 at 2014-06-12 07:18:36
谢谢!
是口服 为什么要研究肝外代谢呢 这个不是研究药物对肝的治疗作用
...

药物还可以在小肠壁 发生代谢,讲解。。。个人意见。
4楼2014-06-14 04:17:15
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