Prostacyclin, its fatty acid precursor and its metabolites on the inotropic function of and on the prostanoid generation by diabetic arteries
Relationships between arachidonic acid (AA) metabolism and contractile responses to Na arachidonate (NaA), to prostacyclin (PGI2) and to some of its metabolites, in mesenteric arteries, isolated from sham operated and from diabetic, totally pancreatectomized dogs, were studied. Arachidonate and pros...
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| Autores principales: | , , , , , |
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| Formato: | JOUR |
| Materias: | |
| Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_0232766X_v43_n8-9_pS257_SterinBorda |
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| Sumario: | Relationships between arachidonic acid (AA) metabolism and contractile responses to Na arachidonate (NaA), to prostacyclin (PGI2) and to some of its metabolites, in mesenteric arteries, isolated from sham operated and from diabetic, totally pancreatectomized dogs, were studied. Arachidonate and prostacyclin enhanced the resting basal tone of preparations from pancreatectomized animals but depressed it in vessels from intact normal controls or from sham operated dogs. Inhibitors of thromboxane A2 (TXA2) biosynthesis, abolished in vitro the vasoconstricting effect of NaA and PGI2 in diabetics; whereas inhibitors of PGI2 biosynthesis blocked the vasodilating influence of NaA in normal mesenterics. Additionally, antagonists of cyclooxygenase activity precluded both the vasoconstricting and vasodilating actions of NaA in normal and in diabetic arteries, respectively, as well as the PGI2 tone enhancement in vessels from diabetics. Blockers of adrenoreceptors and antagonists of lipoxygenases failed to block the positive inotropic effects of PGI2 in mesenterics from diabetic dogs. On the other hand, 6-keto-PGF(1α) did not evoke contractile influences, either in diabetics or in controls, whereas 6-keto-PGE1 induced, in both groups, a dose-dependent relaxation. In arteries from pancreatectomized animals treated with insulin, PGI2 induced a biphasic effect (constriction and relaxation) of magnitudes between those seen in normal controls or sham operated and in untreated diabetics. The basal radio-conversion of exogenous [1-14C]-AA, evidenced that mesenterics from diabetic animals generated more TXB2 than vessels from intact normal control or from sham-operated dogs. Moreover, in the presence of exogenous PGI2, the vascular production of TXB2 from AA in the diabetic group was significantly greater than that of preparations not exposed to PGI2. The % conversion of AA into PGI2 (assessed as 6-oxo-PGF(1α)) was similar in arteries from intact normal controls, from sham operated or from diabetic animals. Insulin given in vivo abolished the greater basal conversion of AA into TXB2 by mesenterics from diabetic dogs and attenuated significantly the enhanced prostacyclin-evoked generation of thromboxane. The present results strongly suggest that the normal tone enhancement evoked by NaA and by PGI2, in mesenteric arteries from diabetic dogs, is presumably related to the generation of TXA2 by vessel walls themselves. |
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