Wagner H R, Davis J N
Proc Natl Acad Sci U S A. 1979 Apr;76(4):2057-61. doi: 10.1073/pnas.76.4.2057.
Rat cerebral cortex slices exposed to (-)-isoproterenol and then washed accumulated significantly less cyclic AMP when rechallenged with isoproterenol than did control slices. The isoproterenol-induced desensitization was associated with a concurrent reduction in [3H]dihydroalprenolol membrane binding but with no change in the affinity of [3H]dihydroalprenolol or isoproterenol for the binding sites. beta-Adrenergic receptor desensitization was rapidly reversed by slice depolarization with high-[K+] buffers, batrachotoxin, grayanotoxin, or veratridine, even in the continued presence of isoproterenol. Restoration of binding by grayanotoxin was prevented by tetrodotoxin or by removing Na+ from the buffer. These data demonstrate partial participation of the membrane receptor in beta-adrenergic desensitization of rat brain slices and suggest that brain beta-adrenergic receptors, like cholinergic receptors in skeletal muscle and alpha-adrenergic receptors in rat parotid, are regulated in part by membrane voltage.
暴露于(-)-异丙肾上腺素后再冲洗的大鼠大脑皮层切片,在再次用异丙肾上腺素刺激时积累的环磷酸腺苷(cAMP)明显少于对照切片。异丙肾上腺素诱导的脱敏与[3H]二氢阿普洛尔膜结合的同时减少有关,但[3H]二氢阿普洛尔或异丙肾上腺素与结合位点的亲和力没有变化。即使在异丙肾上腺素持续存在的情况下,用高钾缓冲液、蝙蝠毒素、灰藓毒素或藜芦碱使切片去极化,也能迅速逆转β-肾上腺素能受体脱敏。河豚毒素或从缓冲液中去除钠离子可阻止灰藓毒素恢复结合。这些数据表明膜受体部分参与了大鼠脑切片的β-肾上腺素能脱敏,并提示脑β-肾上腺素能受体,如骨骼肌中的胆碱能受体和大鼠腮腺中的α-肾上腺素能受体,部分受膜电压调节。