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在大鼠离体后肢中,腺苷和肌苷引起的血管收缩被色胺能机制的阻断所消除。

Vasoconstriction after adenosine and inosine in the rat isolated hindlimb abolished by blockade of tryptaminergic mechanisms.

作者信息

Sakai K, Akima M

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1978 Mar;302(1):55-9. doi: 10.1007/BF00586597.

DOI:10.1007/BF00586597
PMID:652053
Abstract

The isolated right hindlimb of the rat was perfused at a fixed flow rate through the femoral artery with heparinized blood from the carotid artery of a donor. Single injections of adenosine (1--300 microgram) induced a biphasic response, a long-lasting vasoconstriction preceded by a transient vasodilatation. Inosine (1--300 microgram) produced only vasoconstriction. After repeated administration of 300 microgram of these substances, the vasoconstriction became less prominent, and finally reverted to vasodilatation. The vasoconstrictor response to these substances (300 microgram) was also diminished or reverted to vasodilatation after pretreatment with reserpine or methysergide. From these results, it is concluded that vasoconstriction after adenosine or inosine may be mediated by 5-hydroxytryptamine released from the peripheral stores and that the intrinsic direct action of these substances on the femoral vascular bed is vasodilator.

摘要

将大鼠的离体右后肢通过股动脉以固定流速用来自供体颈动脉的肝素化血液进行灌注。单次注射腺苷(1 - 300微克)可诱发双相反应,即短暂的血管舒张之后是持久的血管收缩。肌苷(1 - 300微克)仅产生血管收缩。重复给予300微克这些物质后,血管收缩变得不那么明显,最终转变为血管舒张。在用利血平或甲基麦角新碱预处理后,对这些物质(300微克)的血管收缩反应也减弱或转变为血管舒张。从这些结果可以得出结论,腺苷或肌苷后的血管收缩可能由外周储存释放的5 - 羟色胺介导,并且这些物质对股血管床的内在直接作用是血管舒张剂。

相似文献

1
Vasoconstriction after adenosine and inosine in the rat isolated hindlimb abolished by blockade of tryptaminergic mechanisms.在大鼠离体后肢中,腺苷和肌苷引起的血管收缩被色胺能机制的阻断所消除。
Naunyn Schmiedebergs Arch Pharmacol. 1978 Mar;302(1):55-9. doi: 10.1007/BF00586597.
2
Tryptaminergic mechanism participating in induction of vasoconstriction by adenine nucleotides, adenosine, IMP and inosine in the isolated and blood-perfused hindlimb preparation of the rat.参与腺嘌呤核苷酸、腺苷、肌苷酸和肌苷在大鼠离体和血液灌注后肢制备中诱导血管收缩的色胺能机制。
Jpn J Pharmacol. 1978 Aug;28(4):579-87. doi: 10.1254/jjp.28.579.
3
Role of 5-hydroxytryptamine in the vasoconstrictor action of compound 48/80 in the rat femoral vasculature.5-羟色胺在化合物48/80对大鼠股血管的血管收缩作用中的作用。
Br J Pharmacol. 1979 Mar;65(3):363-6. doi: 10.1111/j.1476-5381.1979.tb07839.x.
4
Tryptaminergic vasoconstriction induced by adenosine in the femoral vascular bed of the rat.腺苷在大鼠股血管床中诱导的色胺能血管收缩。
Jpn J Pharmacol. 1977 Dec;27(6):908-10. doi: 10.1254/jjp.27.908.
5
Femoral vascular responses to purine and pyrimidine derivatives: release of 5-hydroxytryptamine by purine derivatives in isolated, cross-circulated rat hindlimb.股血管对嘌呤和嘧啶衍生物的反应:嘌呤衍生物在离体交叉循环大鼠后肢中释放5-羟色胺。
Jpn J Pharmacol. 1979 Apr;29(2):243-51. doi: 10.1254/jjp.29.243.
6
Adenosine contracts the isolated rat tail artery by releasing endogenous 5-hydroxytryptamine.腺苷通过释放内源性5-羟色胺使离体大鼠尾动脉收缩。
Eur J Pharmacol. 1981 Dec 3;76(2-3):275-7. doi: 10.1016/0014-2999(81)90513-6.
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Modification of the vasomotor actions of methysergide in the femoral arterial bed of the anaesthetized dog by changes in sympathetic nerve activity.通过交感神经活动的改变对麦角新碱在麻醉犬股动脉床血管舒缩作用的影响。
J Auton Pharmacol. 1981 Mar;1(2):127-32. doi: 10.1111/j.1474-8673.1981.tb00504.x.
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Inhibition of sympathetic vasoconstriction in pigs in vivo by the neuropeptide Y-Y1 receptor antagonist BIBP 3226.神经肽Y-Y1受体拮抗剂BIBP 3226对猪体内交感神经血管收缩的抑制作用。
Br J Pharmacol. 1995 Dec;116(7):2971-82. doi: 10.1111/j.1476-5381.1995.tb15952.x.
9
alpha 1- and alpha 2-adrenoceptor stimulation in the isolated perfused hindquarters of the rat: an in vitro model.
J Cardiovasc Pharmacol. 1983 Jul-Aug;5(4):580-5. doi: 10.1097/00005344-198307000-00011.
10
Noradrenaline and adenosine triphosphate as co-transmitters of neurogenic vasoconstriction in rabbit mesenteric artery.去甲肾上腺素和三磷酸腺苷作为兔肠系膜动脉神经源性血管收缩的共递质。
J Physiol. 1985 Oct;367:435-55. doi: 10.1113/jphysiol.1985.sp015834.

引用本文的文献

1
Mast cell amines and inosineinduced vasoconstriction in the rat hind limb.肥大细胞胺和次黄嘌呤诱导大鼠后肢血管收缩。
Mediators Inflamm. 1997;6(2):141-5. doi: 10.1080/09629359791848.
2
Inosine binds to A3 adenosine receptors and stimulates mast cell degranulation.肌苷与A3腺苷受体结合并刺激肥大细胞脱颗粒。
J Clin Invest. 1997 Dec 1;100(11):2849-57. doi: 10.1172/JCI119833.
3
Purine receptors in the rat anococcygeus muscle.大鼠肛尾肌中的嘌呤受体。

本文引用的文献

1
MODE OF ACTION OF ADENINE, URIDINE AND CYTIDINE NUCLEOTIDES AND 2,6-BIS(DIETHANOLAMINO)-4,8-DIPIPERIDINO-PYRIMIDINO(5,4-D)PYRIMIDINE ON THE CORONARY, RENAL AND FEMORAL ARTERIES.腺嘌呤、尿苷和胞苷核苷酸以及2,6-双(二乙醇胺)-4,8-二哌啶基-嘧啶并[5,4-d]嘧啶对冠状动脉、肾动脉和股动脉的作用机制
Arzneimittelforschung. 1964 Nov;14:1252-4.
2
[COMPETITIVE INHIBITION OF CATALYZED ADENOSINE DIFFUSION AS THE MECHANISM OF THE CORONARY DILATING EFFECT OF A PYRIMIDO-PYRIMIDINE DERIVATIVE].[嘧啶-嘧啶衍生物冠状动脉扩张作用机制为催化腺苷扩散的竞争性抑制]
Pflugers Arch Gesamte Physiol Menschen Tiere. 1964 Jul 1;280:141-57.
3
INFLUENCE OF A PYRIMIDOPYRIMIDINE DERIVATIVE ON DEAMINATION OF ADENOSINE BY BLOOD.
J Physiol. 1983 Feb;335:591-608. doi: 10.1113/jphysiol.1983.sp014553.
4
Stimulation of glycogenolysis and vasoconstriction by adenosine and adenosine analogues in the perfused rat liver.腺苷及腺苷类似物对灌注大鼠肝脏糖原分解和血管收缩的刺激作用。
Biochem J. 1987 Nov 15;248(1):35-41. doi: 10.1042/bj2480035.
5
Adenosine constricts the isolated and perfused monkey coronary artery.腺苷可使离体灌注的猴冠状动脉收缩。
Heart Vessels. 1990;5(2):71-5. doi: 10.1007/BF02058320.
6
Role of 5-hydroxytryptamine in the vasoconstrictor action of compound 48/80 in the rat femoral vasculature.5-羟色胺在化合物48/80对大鼠股血管的血管收缩作用中的作用。
Br J Pharmacol. 1979 Mar;65(3):363-6. doi: 10.1111/j.1476-5381.1979.tb07839.x.
一种嘧啶并嘧啶衍生物对血液中腺苷脱氨基作用的影响。
Circ Res. 1964 Jul;15:83-8. doi: 10.1161/01.res.15.1.83.
4
[The elimination of adenosine from the blood under the influence of 2,6-bis(diethanolamino)-4,8-dipiperidinopyrimido-(5,4-d) pyrimidine and papaverine].[在2,6-双(二乙醇氨基)-4,8-二哌啶基嘧啶并(5,4-d)嘧啶和罂粟碱影响下血液中腺苷的消除]
Arzneimittelforschung. 1962 Nov;12:1130-1.
5
Release of serotonin and catecholamines by drugs.药物引起的血清素和儿茶酚胺释放。
Pharmacol Rev. 1962 Dec;14:531-50.
6
Cardiac nucleotides in hypoxia: possible role in regulation of coronary blood flow.缺氧时的心脏核苷酸:在冠状动脉血流调节中的可能作用。
Am J Physiol. 1963 Feb;204:317-22. doi: 10.1152/ajplegacy.1963.204.2.317.
7
[Inosine potentiation of the effect of adenosine on the heart].[肌苷对腺苷心脏效应的增强作用]
Biochem Pharmacol. 1969 Jan;18(1):43-51. doi: 10.1016/0006-2952(69)90007-0.
8
Metabolically linked vasoactive chemicals in local regulation of blood flow.代谢相关血管活性化学物质在局部血流调节中的作用
Physiol Rev. 1968 Oct;48(4):688-707. doi: 10.1152/physrev.1968.48.4.688.
9
Cardiac effects of nucleosides after propranolol treatment of isolated hearts.普萘洛尔处理离体心脏后核苷的心脏效应。
Am J Physiol. 1970 May;218(5):1399-405. doi: 10.1152/ajplegacy.1970.218.5.1399.
10
Uptake and deamination of adenosine by blood. Species differences, effect of pH, ions, temperature and metabolic inhibitors.血液对腺苷的摄取与脱氨作用。种属差异、pH值、离子、温度及代谢抑制剂的影响。
Biochim Biophys Acta. 1969 Oct 7;192(1):124-32. doi: 10.1016/0304-4165(69)90017-8.