چكيده لاتين :
: In the present study, the effect of acute lead exposure in the presence and absence of dopamine or alpha (a)-adrenoceptor agents on contractile response of rat isolated thoracic aorta was studied.
Methods: Male Wistar rats were used in all experiments. Thoracic aorta was carefully removed, cleaned, and cut into 2-mm thick rings. The rings were mounted for measurement of isometric contractions in a tissue bath containing 10 mL of Krebיs solution at 37 - 38 C. The following drugs were used: lead chloride, dopamine, phenylephrine, prazosin, clonidine, yohimbine, and SCH23390. One-way analysis of variance (ANOVA) and Studentיs f-test were used for statistical analyses. P < 0.05 was considered significant.
Results: The ch-adrenoceptor antagonist (prazosin), ci2-adrenoceptor antagonist (yohimbine), or dopamine Di receptor antagonist (SCH23390), did not elicit any response. Combination of lead with dopamine, phenylephrine, or clonidine did not show any potentiation. SCH23390, prazosin, and yohimbine decreased the contraction induced by lead. SCH23390 decreased the contraction induced by dopamine, or lead plus dopamine. Prazosin reduced the contraction induced by phenylephrine or lead plus phenylephrine. Yohimbine attenuated the response induced by clonidine or lead plus clonidine.
Conclusion: CM, a2, and Di dopamine receptor mechanisms could have a role in lead-induced contraction.
