McMurchie E J, Patten G S, McLennan P L, Charnock J S, Nestel P J
CSIRO (Australia), Division of Human Nutrition, Glenthorne Laboratory,O'Halloran Hill.
Biochim Biophys Acta. 1988 Jan 22;937(2):347-58. doi: 10.1016/0005-2736(88)90257-x.
Dietary lipid supplements high in either saturated fat derived from sheep kidney fat or unsaturated fat derived from sunflower seed oil, and a low mixed fat reference diet were fed to marmoset monkeys for 20 months and the effects on cardiac membrane lipid composition, and myocardial catecholamine-stimulated adenylate cyclase and beta-adrenergic receptor binding activity were investigated. For cardiac membranes enriched for beta-adrenergic binding activity, the dietary lipid treatment resulted in small changes in the proportion of saturated to unsaturated fatty acids and substantial changes in the (n - 6) to (n - 3) series of unsaturated fatty acids in the membrane phospholipids. The sheep kidney fat diet increased the cholesterol-to-phospholipid ratio in cardiac membranes in comparison to the other diets. This diet also significantly elevated basal and isoproterenol-, epinephrine- and norepinephrine-stimulated adenylate cyclase activity. The value of the dissociation constant (Kd) and the receptor number (Bmax) for the binding of [125I]ICYP to the beta-adrenergic receptor was significantly reduced in marmosets fed the sheep kidney fat diet. These results suggest that dietary lipids can influence the activity of the beta-adrenergic/adenylate cyclase system of the heart. Modulation of this transmembrane signalling system may be induced by changes in the properties of the associated membrane lipids, particularly by alteration in the membrane cholesterol-to-phospholipid ratio. This effect may be limited to those animal species in which the nature of the dietary fatty acid intake may be influencing cardiac membrane cholesterol homeostasis, which is in agreement with previous results in rats following dietary cholesterol supplementation (McMurchie et al. (1987) Biochim. Biophys. Acta 898, 137-153). ICYP, (-)-iodocyanopindolol.
将富含源自羊肾脂肪的饱和脂肪或源自向日葵籽油的不饱和脂肪的膳食脂质补充剂,以及低混合脂肪参考饮食喂给狨猴20个月,并研究其对心脏膜脂质组成、心肌儿茶酚胺刺激的腺苷酸环化酶和β-肾上腺素能受体结合活性的影响。对于富含β-肾上腺素能结合活性的心脏膜,膳食脂质处理导致膜磷脂中饱和脂肪酸与不饱和脂肪酸比例的微小变化以及不饱和脂肪酸(n - 6)与(n - 3)系列的显著变化。与其他饮食相比,羊肾脂肪饮食增加了心脏膜中的胆固醇与磷脂比率。这种饮食还显著提高了基础以及异丙肾上腺素、肾上腺素和去甲肾上腺素刺激的腺苷酸环化酶活性。喂食羊肾脂肪饮食的狨猴中,[125I]ICYP与β-肾上腺素能受体结合的解离常数(Kd)值和受体数量(Bmax)显著降低。这些结果表明膳食脂质可影响心脏的β-肾上腺素能/腺苷酸环化酶系统的活性。这种跨膜信号系统的调节可能由相关膜脂质性质的变化诱导,特别是膜胆固醇与磷脂比率的改变。这种效应可能仅限于那些膳食脂肪酸摄入性质可能影响心脏膜胆固醇稳态的动物物种,这与先前给大鼠补充膳食胆固醇后的结果一致(McMurchie等人,(1987年)《生物化学与生物物理学报》898,137 - 153)。ICYP,(-)-碘氰吲哚洛尔。