## Abstract We examined the expression and function of β‐adrenergic receptor (β‐AR) subtypes in both isolated primary rat microglia and a rat microglial cell line. RT‐PCR analyses revealed that microglia expressed β~1~‐ and β~2~‐ARs but not β~3~‐ARs, whereas rat primary peritoneal macrophages expre
Differential effects of morphine withdrawal on cerebral β1- and β2-adrenergic receptors
✍ Scribed by Dr. Kinya Kuriyama; Makoto Muramatsu; Seitaro Ohkuma; Jun-Ichi Tamura; Zuo Ping Ping
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 438 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0360-4012
No coin nor oath required. For personal study only.
✦ Synopsis
Effect of morphine dependence and its withdrawal on the 3H-dihydroalprenolol (3H-DHA) binding for @-adrenergic receptors, PI and p2, was examined by a computerized analysis of biphasic Hofstee plots. The relative density of PI and /32 receptors in the rat cerebral cortex was found to be approximately 70% and 30%, respectively. In rats rendered dependent on morphine by a subcutaneous implantation of a morphine pellet, the 3H-DHA binding to @ I and p2 receptors was not altered. During the stage of withdrawal induced by administration of naloxone, however, the 3H-DHA binding t o the cerebral particulate fractions was increased, and this increase was due to the increased binding sites in PI but not in 0 2 receptor. On the other hand, the apparent affinities of @, and p2 receptors for atenolol and salbutamol, selective antagonists for 6,and 62-adrenergic receptors, respectively, were not altered under these experimental conditions. These results suggest that an abrupt increase in cerebral @,-receptor binding sites occurs at morphine withdrawal, and the occurrence of such a supersensitivity in cerebral @, receptor may be involved in the exhibition and/or maintenance of the abstinence syndrome in morphine-dependent subjects.
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