Dax E M, Partilla J S, Piñeyro M A, Gregerman R I
Endocrinology Section, National Institute on Aging, Francis Scott Key Medical Center, Baltimore, Maryland 21224.
Endocrinology. 1990 Nov;127(5):2236-40. doi: 10.1210/endo-127-5-2236.
Glucagon-stimulated adenylyl cyclase activity has been shown to change in liver membranes manipulated to alter either their fatty acid composition or fluidity. We examined whether membrane alterations induced by dietary manipulation affected receptor function. Glucagon- and beta-adrenergic-stimulated receptor-adenylyl cyclase systems were examined in liver membranes of rats fed diets containing 10% corn oil, 10% coconut oil (essential FFA deficient), or 8.5% coconut oil with 1.5% corn oil (essential FFA repleat). Basal and maximal nonreceptor-mediated adenylyl cyclase activity (stimulated by NaF, guanylylimidodiphosphate, and forskolin) was the same in membranes of each of the dietary groups, suggesting that Gs-protein and the catalytic unit activity per se were unaltered by the manipulations. Glucagon-stimulated adenylyl cyclase activity increased with increasing unsaturation of dietary fatty acids; activity in coconut oil-fed rats was 527 +/- 30 (mean +/- SEM) pmol/mg.10 min, that in coconut/corn oil-fed rats was 752 +/- 74 pmol/mg.10 min, and that in corn oil-fed rats was 981 +/- 94 pmol cAMP/mg.10 min. [125I]Monoiodoglucagon binding did not increase in parallel to the adenylyl cyclase alterations; coconut oil-fed animals (614 fmol/mg) differed from the other groups (450 and 430 fmol/mg). Isoproterenol (beta-adrenergic)-stimulated adenylyl cyclase activity was also highest in the corn oil-fed animals, but was similar in the other dietary groups, with no difference in other characteristics of [125I]iodopindolol binding between the groups. The results demonstrate that alterations in the glucagon-stimulated adenylyl cyclase response are different from those in the beta-adrenergic adenylyl cyclase response. Further, they suggest that although direct activations of the catalytic unit or its interaction with the guanine nucleotide-sensitive protein are apparently not affected, hormone receptor-mediated adenylyl cyclase activity may be altered by these dietary manipulations.
已表明,在经过处理以改变其脂肪酸组成或流动性的肝细胞膜中,胰高血糖素刺激的腺苷酸环化酶活性会发生变化。我们研究了饮食操控引起的膜改变是否会影响受体功能。在喂食含10%玉米油、10%椰子油(必需脂肪酸缺乏)或8.5%椰子油与1.5%玉米油(必需脂肪酸补充)饮食的大鼠肝细胞膜中,检测了胰高血糖素和β-肾上腺素能刺激的受体-腺苷酸环化酶系统。每个饮食组膜中的基础和最大非受体介导的腺苷酸环化酶活性(由氟化钠、鸟苷酰亚胺二磷酸和福斯可林刺激)相同,这表明Gs蛋白和催化单位活性本身并未因这些处理而改变。胰高血糖素刺激的腺苷酸环化酶活性随饮食脂肪酸不饱和度的增加而增加;喂食椰子油的大鼠中的活性为527±30(平均值±标准误)pmol/mg·10分钟,喂食椰子油/玉米油的大鼠中的活性为752±74 pmol/mg·10分钟,喂食玉米油的大鼠中的活性为981±94 pmol cAMP/mg·10分钟。[125I]单碘胰高血糖素结合并未与腺苷酸环化酶改变平行增加;喂食椰子油的动物(614 fmol/mg)与其他组(450和430 fmol/mg)不同。异丙肾上腺素(β-肾上腺素能)刺激的腺苷酸环化酶活性在喂食玉米油的动物中也最高,但在其他饮食组中相似,各组之间[125I]碘吲哚洛尔结合的其他特征没有差异。结果表明,胰高血糖素刺激的腺苷酸环化酶反应的改变与β-肾上腺素能腺苷酸环化酶反应的改变不同。此外,它们表明,虽然催化单位的直接激活或其与鸟嘌呤核苷酸敏感蛋白的相互作用显然不受影响,但这些饮食操控可能会改变激素受体介导的腺苷酸环化酶活性。