Desensitization of $A_1$ Adenosine Receptors in Rat Cerebral Cortex

흰쥐 대뇌피질에서 $A_1$ 아데노신 수용체의 탈감작

  • Park, Kyung-Sun (Department of Pharmacology and Institute of Basic Medical Sciences, Wonju College of Medicine) ;
  • Yang, Wan-Suk (Department of Pharmacology and Institute of Basic Medical Sciences, Wonju College of Medicine) ;
  • Kim, Kyung-Hwan (Department of Pharmacology, College of Medicine)
  • 박경선 (연세대학교 원주의과대학 약리학교실 및 기초의학연구소) ;
  • 양완숙 (연세대학교 원주의과대학 약리학교실 및 기초의학연구소) ;
  • 김경환 (연세대학교 의과대학 약리학교실)
  • Published : 1996.09.30

Abstract

Following the subcutaneous administration of $R(-)N^6-(2-phenylisopropyl)adenosine(600\;nmol/kg/hr)$ to rats for 1 week using t$Alzet^{\circledR}$ mini-osmotic pumps, $A_1$ adenosine receptor functions were determined using $[^3H]DPCPX$ binding, $[^{35}S]GTP_{\gamma}S$ binding, and adenylyl cyclase assays. $A_1$ adenosine receptor binding and the inhibition of adenylyl cyclase activity by PIA was not altered in cerebrocortical membranes prepared from PIA-treated rats. However, there was a significant decrease in the $A_1$ adenosine receptor-mediated stimulation of $[^{35}S]GTP_{\gamma}S$ binding to cerebrocortical membranes prepared from PIA-treated rats(22.0% decrease in basal activity; 19.7% decrease in maximal activity). These results suggest that the desensitization of $A_1$ adenosine receptors following chronic administration involves agonist-induced uncoupling of the receptors from G proteins rather than alteration of $A_1$ adenosine receptor molecules. It is also suggested that the determination of stimulation of $[^{35}S]GTP_{\gamma}S$ binding to G proteins is a suitable tool in studying the receptor regulation including desensitization

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