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大鼠体内给药后甘油三硝酸酯和环磷酸鸟苷的组织水平以及耐受性发展的影响。

Tissue levels of glyceryl trinitrate and cGMP after in vivo administration in rat, and the effect of tolerance development.

作者信息

Torfgård K, Ahlner J, Axelsson K L, Norlander B, Bertler A

机构信息

Department of Pharmacology, Faculty of Health Sciences, University Hospital, Linköping, Sweden.

出版信息

Can J Physiol Pharmacol. 1991 Sep;69(9):1257-61. doi: 10.1139/y91-184.

DOI:10.1139/y91-184
PMID:1661636
Abstract

The present study compares the tissue distribution of glyceryl trinitrate (GTN) in plasma, heart, brain, aortic tissue, and adipose tissue from GTN tolerant and GTN nontolerant rats at various time points. Furthermore, the cGMP levels in brain, heart, and aortic tissue were studied at various time points as well as the concentration-effect relationship for GTN in aorta isolated at different time points after the last exposure to GTN. Concentrations of GTN were found to be higher in all tissues studied as compared with plasma, and the concentrations of GTN were higher in tissues from tolerant rats as compared with nontolerant rats, except for aortic tissue. Concentration-effect curves obtained in vitro showed that aortic smooth muscle was still tolerant 24 h after the last dose of GTN. The cGMP level in brain was significantly increased by 40% 2 h after a single dose of GTN (50 mg/kg) and in aortic tissue by 50% at 15 min and at 2 h after a single dose of GTN (50 mg/kg). There was no effect on cGMP in brain, while an increase was seen in aortic tissue 15 min after the last dose in tolerant animals. No change in cGMP level was seen in heart neither in nontolerant nor in tolerant animals at 15 min and at 2 h. No effect on cGMP levels in brain, heart, and aortic tissue was seen 8, 16, and 24 h after exposure to GTN in either tolerant or nontolerant rats. In conclusion, GTN does not involve the cGMP system in heart, and tolerance development caused a less pronounced GTN-induced cGMP increase in aortic tissue.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究比较了在不同时间点,硝酸甘油(GTN)耐受和GTN不耐受大鼠的血浆、心脏、脑、主动脉组织及脂肪组织中GTN的组织分布。此外,还研究了不同时间点脑、心脏和主动脉组织中的cGMP水平,以及在最后一次暴露于GTN后不同时间点分离的主动脉中GTN的浓度-效应关系。结果发现,与血浆相比,所有研究组织中的GTN浓度均较高,除主动脉组织外,耐受大鼠组织中的GTN浓度高于不耐受大鼠。体外获得的浓度-效应曲线显示,在最后一剂GTN后24小时,主动脉平滑肌仍具有耐受性。单次给予GTN(50mg/kg)后2小时,脑中的cGMP水平显著升高40%,单次给予GTN(50mg/kg)后15分钟和2小时,主动脉组织中的cGMP水平升高50%。在耐受动物中,末次给药后15分钟,脑内cGMP无变化,而主动脉组织中cGMP升高。在15分钟和2小时时,无论是不耐受还是耐受动物,心脏中的cGMP水平均无变化。在耐受或不耐受大鼠中,暴露于GTN后8、16和24小时,脑、心脏和主动脉组织中的cGMP水平均无影响。总之,GTN不涉及心脏中的cGMP系统,耐受性的发展导致GTN诱导的主动脉组织中cGMP升高不明显。(摘要截断于250字)

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引用本文的文献

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Differential nitros(yl)ation of blood and tissue constituents during glyceryl trinitrate biotransformation in vivo.体内三硝酸甘油酯生物转化过程中血液和组织成分的差异性亚硝基化作用
Proc Natl Acad Sci U S A. 2004 Nov 30;101(48):16958-63. doi: 10.1073/pnas.0406075101. Epub 2004 Nov 18.
2
Direct myocardial anti-ischaemic effect of GTN in both nitrate-tolerant and nontolerant rats: a cyclic GMP-independent activation of KATP.硝酸甘油对硝酸酯耐受和非耐受大鼠心肌的直接抗缺血作用:一种不依赖环磷酸鸟苷的三磷酸腺苷敏感性钾通道激活。
Br J Pharmacol. 1999 Dec;128(7):1427-34. doi: 10.1038/sj.bjp.0702929.