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注入大鼠体内的血清素的身体分布情况。

Body distribution of infused serotonin in rats.

作者信息

Linder A Elizabeth, Beggs Kevin M, Burnett Robert J, Watts Stephanie W

机构信息

Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan 48824, USA.

出版信息

Clin Exp Pharmacol Physiol. 2009 May;36(5-6):599-601. doi: 10.1111/j.1440-1681.2009.05147.x. Epub 2009 Jan 18.

Abstract
  1. Our goal was to investigate the body distribution of serotonin (5-hydroxytryptamine; 5-HT) in rats infused with 5-HT (25 microg/kg per min) for 7 days and the contribution of the 5-HT transporter (SERT) for 5-HT uptake into the tissues. 2. Mini-osmotic pumps containing 5-HT or vehicle were implanted in rats knocked out for SERT (SERT-KO) or in wild-type (WT) rats. On the 8th day, tissues were harvested for measurements of 5-HT by high-performance liquid chromatography (HPLC). The 5-HT metabolite 5-hydroxyindole acetic acid (5-HIAA) was also measured by HPLC, because an increase in 5-HIAA in tissues from rats receiving 5-HT reflects 5-HT uptake followed by metabolism. 3. In WT rats infused with 5-HT, an increase in 5-HT or 5-HIAA was observed in the heart, pancreas, thyroid, adrenal gland, kidney, seminal vesicle, bladder, prostate, liver, oesophagus, stomach, femur, trachea, lung and spleen compared with vehicle-infused rats. An increase in 5-HT and 5-HIAA was not observed in aorta, vena cava and jejunum. In tissues from SERT-KO rats infused with 5-HT, the content of 5-HT or 5-HIAA was decreased in most of the tissues studied compared with 5-HT-infused WT rats. Although 5-HT uptake in the kidney, seminal vesicle, prostate, jejunum and trachea is SERT dependent, it is SERT independent in the pancreas. The remaining tissues display SERT-dependent and -independent mechanisms for 5-HT uptake. 4. Altogether, tissues from different systems, such as the cardiovascular, endocrine, genitourinary and gastrointestinal, accumulate 5-HT mainly via SERT and, thus, these systems are potential targets for drugs that interfere with 5-HT homeostasis.
摘要
  1. 我们的目标是研究连续7天输注5-羟色胺(5-羟色胺;5-HT,25微克/千克每分钟)的大鼠体内5-HT的分布情况,以及5-HT转运体(SERT)对组织摄取5-HT的作用。2. 将含有5-HT或赋形剂的微型渗透泵植入SERT基因敲除(SERT-KO)大鼠或野生型(WT)大鼠体内。在第8天,采集组织,通过高效液相色谱法(HPLC)测量5-HT。还通过HPLC测量5-HT代谢产物5-羟吲哚乙酸(5-HIAA),因为接受5-HT的大鼠组织中5-HIAA的增加反映了5-HT摄取后随之发生的代谢过程。3. 在输注5-HT的WT大鼠中,与输注赋形剂的大鼠相比,在心脏、胰腺、甲状腺、肾上腺、肾脏、精囊、膀胱、前列腺、肝脏、食管、胃、股骨、气管、肺和脾脏中观察到5-HT或5-HIAA增加。在主动脉、腔静脉和空肠中未观察到5-HT和5-HIAA增加。在输注5-HT的SERT-KO大鼠的组织中,与输注5-HT的WT大鼠相比,在大多数研究的组织中5-HT或5-HIAA的含量降低。尽管肾脏、精囊、前列腺、空肠和气管中的5-HT摄取依赖于SERT,但胰腺中的5-HT摄取不依赖于SERT。其余组织显示出5-HT摄取的SERT依赖性和非依赖性机制。4. 总之,心血管、内分泌、泌尿生殖和胃肠道等不同系统的组织主要通过SERT积累5-HT;因此,这些系统是干扰5-HT稳态药物的潜在靶点。

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