Fredholm B B
Acta Physiol Scand. 1982 Jun;115(2):283-6. doi: 10.1111/j.1748-1716.1982.tb07078.x.
After one week treatment with caffeine (20 mg/kg i.p.) the number of adenosine receptors, as determined by specific binding of (3H)-L-PIA, in rat cerebral cortical membranes was increased by about 25%. Cyclic AMP accumulation induced by adenosine analogues in slices of rat hippocampus was unaffected by caffeine treatment. The inhibition of lipolysis in rat fat cells by 2-chloro-adenosine was similarly unaffected. The potency of caffeine as an antagonist of these adenosine-receptor mediated effects was not altered by caffeine treatment. It is concluded that at least some adenosine receptors are up-regulated as a consequence of prolonged caffeine treatment, but that the increase in receptor number is not related to changes in at least two effects of adenosine and caffeine.
用咖啡因(20毫克/千克腹腔注射)治疗一周后,通过(3H)-L-PIA的特异性结合测定,大鼠大脑皮质膜中腺苷受体的数量增加了约25%。咖啡因处理对腺苷类似物在大鼠海马切片中诱导的环磷酸腺苷积累没有影响。2-氯腺苷对大鼠脂肪细胞脂解的抑制作用同样不受咖啡因处理的影响。咖啡因作为这些腺苷受体介导效应拮抗剂的效力并未因咖啡因处理而改变。结论是,长期咖啡因治疗导致至少一些腺苷受体上调,但受体数量的增加与腺苷和咖啡因至少两种效应的变化无关。