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O-(β-羟乙基)芦丁(HR)对大鼠皮肤毛细血管抵抗力的影响。

The effect of O-(beta-hydroxyethyl)-rutosides (HR) on the skin capillary resistance of rats.

作者信息

Gábor M

出版信息

Arzneimittelforschung. 1981;31(3):442-5.

PMID:7194669
Abstract

The effect of three different oral doses of O-(beta-hydroxyethyl)-rutosides (HR, Venoruton) on the skin capillary resistance (CR) of Sprague-Dawley rats aged 8-10 weeks, 6 months or 1 year (and selected because of their low CR) was investigated. The CR was measured over a period of 24 h after a single administration of each dose. The results were compared with a further group aged 6 months who received HR intraperitoneally. The optimal dose was defined in all four groups receiving the drug systemically. In most cases a significant effect could be shown already after 2-4 h, persisting until at least 8 h and in some cases 24 h. Comparative data were also obtained with four different pure hydroxyethyl components (tetra-HR, tri-HR, di-HR and mono-7-HR) in identical experimental conditions. The most active appeared to be the mono-7-HR. Finally, the effect of a single topical application of a gel containing 2% HR was investigated. This produced a significant increase of CR after 1 h, which lasted around 4-5 h. The clinical implications of these results are discussed with special reference to senile, hypertensive and diabetic vascular disease.

摘要

研究了三种不同口服剂量的O-(β-羟乙基)-芦丁(HR,维脑路通)对8 - 10周龄、6个月龄或1岁的斯普拉格-道利大鼠(因其皮肤毛细血管阻力低而选取)皮肤毛细血管阻力(CR)的影响。在单次给予每种剂量后24小时内测量CR。将结果与另一组接受腹腔注射HR的6个月龄大鼠进行比较。在所有全身接受药物治疗的四组中确定了最佳剂量。在大多数情况下,给药后2 - 4小时即可显示出显著效果,持续至至少8小时,在某些情况下持续24小时。在相同实验条件下,还获得了四种不同的纯羟乙基成分(四-HR、三-HR、二-HR和单-7-HR)的比较数据。活性最强的似乎是单-7-HR。最后,研究了单次局部应用含2% HR的凝胶的效果。1小时后CR显著增加,持续约4 - 5小时。特别参照老年、高血压和糖尿病血管疾病讨论了这些结果的临床意义。

相似文献

1
The effect of O-(beta-hydroxyethyl)-rutosides (HR) on the skin capillary resistance of rats.O-(β-羟乙基)芦丁(HR)对大鼠皮肤毛细血管抵抗力的影响。
Arzneimittelforschung. 1981;31(3):442-5.
2
Metabolism of hydroxyethylrutosides (HR): metabolism of [14C]-HR in man.羟乙基芦丁(HR)的代谢:人体内[14C]-HR的代谢
Arzneimittelforschung. 1976;26(5):925-8.
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Pharmacokinetics of mono-3'- and mono-4'-0-(beta-hydroxyethyl)-rutoside derivatives, after single doses of Venoruton powder in healthy volunteers.
Eur J Clin Pharmacol. 2002 Sep;58(6):395-402. doi: 10.1007/s00228-002-0472-3. Epub 2002 Aug 2.
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[Capillary resistance raising action of Venoruton. Experimental data on the therapeutic effects of Venoruton].[维脑路通的毛细血管阻力增强作用。关于维脑路通治疗效果的实验数据]
Acta Pharm Hung. 1983 May;53(3):115-20.
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5-Year control and treatment of edema and increased capillary filtration in venous hypertension and diabetic microangiopathy using O-(beta-hydroxyethyl)-rutosides: a prospective comparative clinical registry.使用 O-(β-羟乙基)-芦丁苷对静脉高压和糖尿病微血管病变中的水肿及毛细血管滤过增加进行 5 年的对照与治疗:一项前瞻性比较临床注册研究。
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[Studies in animal experiments on determination of blood and organ levels of o-(beta-hydroxyethyl)-rutosides (HR) after i.p. administration (author's transl)].[腹腔注射后o-(β-羟乙基)-芦丁糖苷(HR)血药浓度及脏器浓度测定的动物实验研究(作者译)]
Arzneimittelforschung. 1980;30(4):657-9.
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[Chromatographic studies of four water-soluble rutosides].[四种水溶性芸香苷的色谱研究]
Arzneimittelforschung. 1975 Apr;25(4):511-6.
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O-(beta-hydroxyethyl)-rutosides systemic and local treatment in chronic venous disease and microangiopathy: an independent prospective comparative study.O-(β-羟乙基)-芦丁苷对慢性静脉疾病和微血管病变的全身及局部治疗:一项独立前瞻性对照研究。
Angiology. 2008 Feb-Mar;59 Suppl 1:7S-13S. doi: 10.1177/0003319707312021.
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Protective effects of O-(beta-hydroxyethyl)-rutosides (HR) against adriamycin-induced toxicity in rats.O-(β-羟乙基)芦丁(HR)对阿霉素诱导的大鼠毒性的保护作用。
Arch Int Pharmacodyn Ther. 1985 Feb;273(2):323-34.
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The effect of O-(beta-hydroxyethyl)-rutosides on function and structure of the ganglion cells.O-(β-羟乙基)芦丁对神经节细胞功能和结构的影响。
Arzneimittelforschung. 1976;26(9):1645-50.

引用本文的文献

1
Hydroxyethylrutosides. A review of its pharmacology, and therapeutic efficacy in venous insufficiency and related disorders.
Drugs. 1992 Dec;44(6):1013-32. doi: 10.2165/00003495-199244060-00009.