Effect of Ocimum basilicum L. on cyclo-oxygenase isoforms and prostaglandins involved in thrombosis

被引:21
|
作者
Umar, Anwar [1 ,2 ]
Zhou, Wenting [1 ]
Abdusalam, Elzira [1 ]
Tursun, Arzigul [3 ]
Reyim, Nadira [4 ]
Tohti, Ibadet [1 ]
Moore, Nicholas [1 ,2 ]
机构
[1] Xinjiang Med Univ, Dept Pharmacol, Urumqi 830011, Peoples R China
[2] Univ Bordeaux Segalen, Dept Pharmacol, F-33076 Bordeaux, France
[3] Xinjiang Med Univ, Affiliated Hosp 1, Med Res Ctr, Urumqi 830054, Peoples R China
[4] Xinjiang Med Univ, Affiliated Hosp 2, Dept Cardiovasc Internal Med, Urumqi 830063, Xinjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Ocimum basilicum L; In vitro; HUVEC; Macrophage; 6-keto-PGF(1 alpha); PGE2; IN-VITRO; PLATELET-AGGREGATION; COX-2; INHIBITORS; E-2; PRODUCTION; EXPRESSION; NSAIDS; RATS; ARMAGNAC; MODEL; LIPOPOLYSACCHARIDE;
D O I
10.1016/j.jep.2013.12.051
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Ocimum basilicum L. (OBL) is a plant used in traditional Uyghur medicine for the treatment and prevention of cardiovascular disease. In previous studies we had found an antihypertensive and antithrombotic effect suggestive of an effect on prostaglandins, which we attempt to document here. Materials and methods: 6-keto-PGF(1)alpha, the metabolite of prostacyclin, and PGE(2) were measured in the supernatant of human umbilical vein endothelial cells (HUVEC) and basal or LPS-stimulated mouse coeliac macrophage cultures exposed to OBL ethanol (OBL-E) extracts and petroleum ether, chloroform, ethylacetate and butanol (PE, C, EA, B) fractions. In addition, 6-keto-PGF(1)alpha and thromboxane B2 (TXB2) were measured in a rat model of thromboangiitis obliterans exposed or not to OBL. Results: Short-term exposure to OBL-E dose-dependently increased 6-keto-PGF(1)alpha from HUVEC, and long-term (24 h) exposure decreased it. OBL-C and OBL-B increased 6-keto-PGF(1)alpha, whereas the other fractions tended to decrease it after 24 h exposure. The extract and all fractions decreased basal and stimulated PGE2 production, but only OBL-EA and OBL-B reduced PGE2 in stimulated cultures to concentrations below the unstimulated values (P < 0.05). In vivo OBL increased 6-keto-PGF(1)alpha and decreased TXB2. Conclusion: OBL and its extracts increased 6-keto-PGF(1)alpha and reduced PGE2 and TXB2 production in a dose and time-related manner. This could indicate simultaneous inhibition of COX-2 and stimulation of endothelial COX-1. The butanol fraction seemed most promising in this respect. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:151 / 155
页数:5
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