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Renal- and calcium-dependent vascular effects of Polybia paulista wasp venom
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نویسنده
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vinhote j.f.c. ,torres a.f.c. ,dantas r.t. ,praciano t.p. ,menezes r.r.p.p.b. ,sousa d.f. ,brito t.s. ,lima f.j.b. ,toyama m.h. ,magalhães p.j. ,monteiro h.a.s. ,martins-nunes a.m.c.
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منبع
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journal of venomous animals and toxins including tropical diseases - 2011 - دوره : 17 - شماره : 2 - صفحه:199 -208
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چکیده
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In the present study,the effects of polybia paulista venom (ppv) on renal and vascular tissues were investigated. isolated kidneys perfused with ppv (1 and 3 μg/ml) had increased perfusion pressure,renal vascular resistance,urinary flow,and glomerular filtration rate; and reduced sodium tubular transport. histological evaluation demonstrated deposits of proteins in bowman's space and tubular lumen,and focal areas of necrosis. the venom promoted a cytotoxic effect on madin-darby canine kidney (mdck) cells. a significant increase in lactic dehydrogenase levels was observed in response to venom exposure. in isolated mesenteric vascular beds,pressure and vascular resistance augmented in a dose-dependent manner. ppv increased the contractility of aortic rings maintained under basal tension. this contractile response was inhibited when preparations were maintained in ca2+-free medium. likewise,verapamil,a voltage-gated calcium channel blocker,also inhibited the contractile response. in this study,phentolamine,a blocker of α-adrenergic receptor blocker,significantly reduced the contractile effect of ppv in the aortic ring. in conclusion,ppv produced nephrotoxicity,which suggests a direct effect on necrotic cellular death in renal tubule cells. the vascular contractile effect of ppv appears to involve calcium influx through voltage-gated calcium channels via adrenergic regulation. © cevap 2011.
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کلیدواژه
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Aorta; Kidney; MDCK; Polybia paulista; Venom
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آدرس
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department of physiology and pharmacology,federal university of ceará,fortaleza, Brazil, department of clinical and toxicological analyses,federal university of ceará,fortaleza,ceará state, Brazil, department of physiology and pharmacology,federal university of ceará,fortaleza, Brazil, department of clinical and toxicological analyses,federal university of ceará,fortaleza,ceará state, Brazil, department of physiology and pharmacology,federal university of ceará,fortaleza, Brazil, department of physiology and pharmacology,federal university of ceará,fortaleza, Brazil, department of physiology and pharmacology,federal university of ceará,fortaleza, Brazil, department of physiology and pharmacology,federal university of ceará,fortaleza, Brazil, são paulo experimental coast campus,são paulo state university (unesp - univ estadual paulista),são vicente,são paulo state, Brazil, department of physiology and pharmacology,federal university of ceará,fortaleza, Brazil, department of physiology and pharmacology,federal university of ceará,fortaleza, Brazil, department of clinical and toxicological analyses,federal university of ceará,fortaleza,ceará state, Brazil
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Authors
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