Ohisalo J J, Ranta S, Huhtaniemi I T
J Clin Endocrinol Metab. 1984 Jan;58(1):32-5. doi: 10.1210/jcem-58-1-32.
Lipolysis and cAMP accumulation were inhibited by low concentrations of adenosine and its analogs in human sc adipocytes stimulated by 2 microM DL-isoproterenol. The order of potency of the adenosine analogs tested was N6-(phenylisopropyl)adenosine greater than 2-chloroadenosine greater than 5'-N-ethylcarboxamidoadenosine greater than adenosine greater than 2',5'-dideoxyadenosine greater than 2'-deoxyadenosine. Inosine was without effect. No stimulation of cAMP accumulation by 5'-N-ethylcarboxamidoadenosine was observed. These results strongly suggest the presence of inhibitory adenosine Ri- and P-sites and the absence of stimulatory Ra-sites in human sc adipocytes.
在由2 microM DL-异丙肾上腺素刺激的人皮下脂肪细胞中,低浓度的腺苷及其类似物可抑制脂肪分解和环磷酸腺苷(cAMP)的积累。所测试的腺苷类似物的效力顺序为:N6-(苯异丙基)腺苷>2-氯腺苷>5'-N-乙基羧酰胺腺苷>腺苷>2',5'-二脱氧腺苷>2'-脱氧腺苷。肌苷无作用。未观察到5'-N-乙基羧酰胺腺苷对cAMP积累有刺激作用。这些结果有力地表明,人皮下脂肪细胞中存在抑制性腺苷Ri位点和P位点,而不存在刺激性Ra位点。