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Effects of S-adenosyl-L-methionine on platelet thromboxane and vascular prostacyclin
Affiliation:1. Instituto de Fisiología Experimental, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, CONICET, Suipacha 570, 2000 Rosario, Argentina;2. Department of Clinical Pharmacology and Pharmacoepidemiology, University of Heidelberg, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany;1. 54 Rue de la Glacière, 75013 Paris, France;2. 13765 Seabiscuit Drive, Reno, NV, USA;3. GE Healthcare Life Sciences, Maynard Centre, Forest Farm, Whitchurch, Cardiff CF14 7YT, UK
Abstract:We therefore designed the present study to evaluate the effect of S-adenosyl-L-methionine (SAMe) on the synthesis of platelet thromboxane and vascular prostacyclin. The experimental materials were human blood and aortic rings from untreated Wistar rats; and platelets and aortic rings from Wistar rats treated for 7 days with SAMe at 5 or 10 mg/kg/day s.c. The administration of 10 mg/Kg/day of SAMe to rats significantly increased vascular production of 6-keto-PGF. In vitro vascular production of 6-keto-PGF increased in a concentration-dependent manner when SAMe was incubated in the range of 10−7 to 10−4 M. The greatest increase was 167 ± 15%, obtained in samples incubated with 5 × 10−5M SAMe. In aortic rings, lipid peroxidase production was inhibited in a concentration-dependent manner in the SAMe range of 10−7 to 10−5 M. Maximum inhibition (75.3 ± 6.2%) was obtained with SAMe at 1.5 × 10−5M. Vascular 6-keto-PGF production showed a significant inverse linear correlation with vascular lipid peroxide production (Y = −0.04 × + 18.1, r = 0.7309, P < 0.0001).
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