Pariza M W, Butcher F R, Becker J E, Potter V R
Proc Natl Acad Sci U S A. 1977 Jan;74(1):234-7. doi: 10.1073/pnas.74.1.234.
Liver cells were obtained from adult rats by a collagenase perfusion technique and cultured as monolayers in serum-free media. Epinephrine and isoproterenol both induced large increases in intracellular adenosine 3':5'-monophosphate (cAMP) within 1-2 min whereas epinephrine (but not isoproterenol) induced 2- to 3-fold increases in the rate of alpha-aminoisobutyric acid transport within 2-4 hr after a 1 hr lag. Propranolol abolished the increase in cAMP elicited by epinephrine and isoproterenol, but did not block the induction of alpha-aminoisobutyric acid transport by epinephrine. In contrast, dihydroergotamine abolished and phentolamine diminished the induction of alpha-aminoisobutyric acid transport by epinephrine but did not decrease the stimulation of cAMP levels by epinephrine. Epinephrine dose response curves for cAMP and alpha-aminoisobutyric acid transport were similar. Once exposed to epinephrine, cells became refractory to further stimulation of cAMP levels by epinephrine.
采用胶原酶灌注技术从成年大鼠获取肝细胞,并在无血清培养基中单层培养。肾上腺素和异丙肾上腺素均可在1至2分钟内使细胞内3':5'-单磷酸腺苷(cAMP)大幅增加,而肾上腺素(而非异丙肾上腺素)在1小时延迟后2至4小时内可使α-氨基异丁酸转运速率提高2至3倍。普萘洛尔可消除肾上腺素和异丙肾上腺素引起的cAMP增加,但不阻断肾上腺素诱导的α-氨基异丁酸转运。相反,双氢麦角胺可消除肾上腺素诱导的α-氨基异丁酸转运,酚妥拉明可使其减弱,但二者均不降低肾上腺素对cAMP水平的刺激。肾上腺素对cAMP和α-氨基异丁酸转运的剂量反应曲线相似。一旦暴露于肾上腺素,细胞对肾上腺素进一步刺激cAMP水平变得不敏感。