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有证据表明,S-腺苷-L-蛋氨酸非对映异构体可能通过与离体大鼠肝脏中的嘌呤受体相互作用来减轻缺血再灌注损伤。

Evidence that S-adenosyl-L-methionine diastereoisomers may reduce ischaemia-reperfusion injury by interacting with purinoceptors in isolated rat liver.

作者信息

Dunne J B, Alexander B, Williams R, Tredger J M

机构信息

Institute of Liver Studies, Academic Department of Surgery, King's College Hospital and School of Medicine and Dentistry, London.

出版信息

Br J Pharmacol. 1998 Sep;125(1):225-33. doi: 10.1038/sj.bjp.0702043.

DOI:10.1038/sj.bjp.0702043
PMID:9776364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1565596/
Abstract
  1. Mechanisms underlying the haemodynamic activity of diastereoisomers of S-adenosyl-L-methionine (SAM) were investigated using inhibitors of purinoceptors and nitric oxide (NO) synthase in perfused rat livers damaged by sequential 24 h cold and 20 min rewarming ischaemia + reperfusion. 2. Stored livers were flushed with 10 ml saline alone (control) or with added (R,S) or (S,S) SAM (100 microM) and reperfused in the absence (control) or presence of 10 microM 8-phenyltheophylline (8-PT) or 100 microM L-N-monomethylarginine (L-NMMA). 3. Both SAM diastereoisomers rapidly increased blood flow and bile production versus controls (P<0.001) but the (R,S) isomer induced greater increases in blood flow and the (S,S) isomer greater increases in bile production: 625 versus 596 versus 518 ml blood flow and 100 versus 119 versus 56 mg bile production per g liver over 3 h in (R,S), (S,S) and control, respectively. 4. 8-PT prevented the enhancement of blood flow by (S,S) SAM (529 versus 596 ml g(-1) liver over 3 h for (S,S) SAM alone, P<0.001), but was without effect in control livers. 8-PT also reduced SAM-enhanced bile production: 51 versus 119 mg g(-1) liver over 3 h, P<0.001. L-NMMA reduced blood flow and bile production similarly in the absence or presence of (S,S) SAM. 5. Thus, SAM may improve liver perfusion after ischaemia-reperfusion injury via stimulation of P, (A2) purinoceptors at which SAM shows activity. The choleretic activity of (S,S) SAM is disproportionately greater than enhanced blood flow and may occur independently of a NO-dependent component of bile production.
摘要
  1. 利用嘌呤受体抑制剂和一氧化氮(NO)合酶,在经24小时冷缺血及20分钟复温缺血+再灌注损伤的灌注大鼠肝脏中,研究了S-腺苷-L-甲硫氨酸(SAM)非对映异构体血流动力学活性的潜在机制。2. 将保存的肝脏单独用10毫升生理盐水冲洗(对照),或添加(R,S)或(S,S)SAM(100微摩尔)冲洗,并在不存在(对照)或存在10微摩尔8-苯基茶碱(8-PT)或100微摩尔L-N-单甲基精氨酸(L-NMMA)的情况下进行再灌注。3. 与对照组相比,两种SAM非对映异构体均能迅速增加血流量和胆汁生成(P<0.001),但(R,S)异构体引起的血流量增加更大,(S,S)异构体引起的胆汁生成增加更大:在(R,S)、(S,S)和对照组中,每克肝脏在3小时内的血流量分别为625、596和518毫升,胆汁生成分别为100、119和56毫克。4. 8-PT可阻止(S,S)SAM增强血流量(单独使用(S,S)SAM时,3小时内每克肝脏血流量为529对596毫升,P<0.001),但对对照肝脏无影响。8-PT还降低了SAM增强的胆汁生成:3小时内每克肝脏为51对119毫克,P<0.001。在不存在或存在(S,S)SAM的情况下,L-NMMA同样降低了血流量和胆汁生成。5. 因此,SAM可能通过刺激P(A2)嘌呤受体来改善缺血再灌注损伤后的肝脏灌注,SAM在该受体上表现出活性。(S,S)SAM的利胆活性比增强的血流量大得多,可能独立于胆汁生成的NO依赖性成分而发生。

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Purinergic signalling in the liver in health and disease.健康与疾病状态下肝脏中的嘌呤能信号传导
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S-adenosyl methionine (SAMe) versus celecoxib for the treatment of osteoarthritis symptoms: a double-blind cross-over trial. [ISRCTN36233495].S-腺苷甲硫氨酸(SAMe)与塞来昔布治疗骨关节炎症状的比较:一项双盲交叉试验。[国际标准随机对照试验编号:ISRCTN36233495]
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