Effect of apelin on cardiac contractility in acute reno-vascular hypertension: The role of apelin receptor and kappa opioid receptor heterodimerization

Objective(s): Apelin/APJ system plays an important role in the regulation of myocardial contractility (MC) and blood pressure. Opioid receptors (OPRs) are also important cardiovascular regulators and exert many of their effects through modulating the function of other systems. This study analyzed the interaction between APJ and kappa OPRs (KOR) in cardiac responsiveness to apelin in acute reno-vascular hypertension (۲K۱C).Materials and Methods: MC studies were carried out on ۲K۱C rats. F۱۳A (APJ blocker), Naloxone (OPR inhibitor), nor-Binaltorphiminedihydrochloride (nor-BNI; kappa OPR inhibitor), PTX (Gi path inhibitor) and chelerytrine (protein kinase C; PKC inhibitor) were administered prior to apelin ۲۰ and ۴۰ μg/kg. The phosphorylation of extracellular signal–regulated kinases (ERK۱/۲) (PERK) was also assessed. Dimerization of APJ and KOR was evaluated by immunoprecipitation.Results: Both doses of apelin reduced blood pressure. Apelin ۴۰ exerted a negative inotropic effect, which was inhibited by nor-BNI, but apelin ۲۰ showed a positive inotropic effect, which was resistant to this inhibition. Hypertension increased heterodimerization of the APJ and KOR and this was reduced by apelin ۲۰. F۱۳A, naloxone and PTX significantly reduced PERK in apelin ۴۰ group, but F۱۳A, naloxone, and chelerytrine significantly increased PERK in the apelin ۲۰ group.Conclusion: The lowering effect of apelin ۴۰ on MC and its non-effectiveness on APJ/KOR dimerization, while augmenting the contractility and reducing the dimerization by apelin ۲۰ implies the APJ/KOR-related effects of apelin on the MC under acute reno-vascular hypertension. This may have potential clinical applications as apelin has been introduced as a potential therapeutic agent in heart failure and opioids are being currently used in the treatment of myocardial infarction.

Keywords:

Apelin receptors , Dimerization , Myocardium , Opioid receptors , Reno-vascular hypertension