Key result
Chemical sympathectomy with 6-hydroxydopamine increased cardiac beta-adrenergic responsiveness and the number of beta-adrenoceptor binding sites by 52% (P<0.05) in guinea-pigs.
Why the study?
Does chemical sympathectomy with 6-OHDA alter alpha 1- and beta-adrenoceptor responsiveness and binding in guinea-pig cardiac tissues?
Does chemical sympathectomy with 6-OHDA alter alpha 1- and beta-adrenoceptor responsiveness and binding in guinea-pig cardiac tissues?
Sympathetic innervation regulates cardiac beta-adrenergic but not alpha 1-adrenergic responsiveness in guinea-pigs.
Answers are grounded in this paper and cite their sources.
Sympathetic innervation differentially regulates guinea-pig cardiac beta- versus alpha1-adrenoceptors; leaves open translation to human heart failure therapies.
Alpha 1- and beta-adrenoceptor responsiveness and binding have been examined in cardiac tissues removed from guinea-pigs pretreated with 6-hydroxydopamine (6-OHDA) for 3 weeks. Results were compared with control tissues from sham-injected animals. Chemical sympathectomy with 6-OHDA resulted in an increase in the sensitivity of postjunctional beta-adrenoceptor-mediated responses to isoprenaline. No such increase was observed for the alpha 1-adrenoceptor-mediated responses to methoxamine. The increase in beta-adrenergic responsiveness was accompanied by a significant (P less than 0.05) 52% increase in the number of [3H]-dihydroalprenolol binding sites with no change in binding affinity. [3H]-Prazosin binding was not affected by pretreatment with 6-OHDA. The results suggest that cardiac beta- but not alpha 1-adrenergic responsiveness is regulated by the sympathetic innervation.
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Chess‐Williams et al. (1987) studied this question. 6-hydroxydopamine (6-OHDA) vs. Sham-injected animals was evaluated on Beta-adrenergic responsiveness and number of [3H]-dihydroalprenolol binding sites (p=<0.05). Chemical sympathectomy with 6-hydroxydopamine increased cardiac beta-adrenergic responsiveness and the number of beta-adrenoceptor binding sites by 52% (P<0.05) in guinea-pigs.
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