Houseknecht K L, Bauman D E, Carey G B, Mersmann H J
Department of Animal Science, Cornell University, Ithaca, NY, USA.
Domest Anim Endocrinol. 1995 Oct;12(4):325-36. doi: 10.1016/0739-7240(95)00029-e.
Lactating Holstein cows were used to assess the effect of bovine somatotropin (bST; n = 8) and fasting (FAST; n = 4) on ligand binding to beta-adrenergic (BAR) and Type-1 adenosine (A1R) receptors in adipose tissue. Cows received exogenous bST (sometribove; 40 mg/d) or no hormone (control) for 4 d in a single-reversal design with a 7-d interval between treatment periods. Subcutaneous adipose tissue biopsies were taken on day 4 of each treatment. Eight d after the bST regimen, 4 cows were fasted for 3 d and adipose biopsies were taken. Ligand binding was quantified with a postnuclear, total adipose tissue membrane preparation (100,000 x g pellet). Binding to BAR and A1R was assessed with the antagonists [125I]iodocyanopindolol (ICP) and [3H]8-cyclopentyl-1,3-dipropylxanthine (DCPCX), respectively. The binding affinity (Kd) of BAR for ICP was not affected by bST but was enhanced by FAST; maximal binding (Bmax) was increased with bST treatment (P < 0.06) and reduced by FAST (61%, P < 0.01). Kd values for DCPCX binding to A1R were not changed by bST or FAST. bST did not affect Bmax for A1R; however, FAST reduced the Bmax by 38%. Data highlight the differential regulation of BAR and A1R by bST and FAST.
选用泌乳期荷斯坦奶牛来评估牛生长激素(bST;n = 8)和禁食(FAST;n = 4)对脂肪组织中β-肾上腺素能(BAR)和1型腺苷(A1R)受体配体结合的影响。奶牛采用单逆转设计接受外源性bST(司美格鲁肽;40 mg/d)或不接受激素(对照),治疗期之间间隔7天,持续4天。在每种治疗的第4天采集皮下脂肪组织活检样本。bST治疗方案8天后,4头奶牛禁食3天并采集脂肪活检样本。用核后全脂肪组织膜制剂(100,000×g沉淀)对配体结合进行定量。分别用拮抗剂[125I]碘氰吲哚洛尔(ICP)和[3H]8-环戊基-1,3-二丙基黄嘌呤(DCPCX)评估与BAR和A1R的结合。BAR对ICP的结合亲和力(Kd)不受bST影响,但禁食可增强该亲和力;最大结合量(Bmax)在bST治疗后增加(P < 0.06),禁食使其降低(61%,P < 0.01)。DCPCX与A1R结合的Kd值不受bST或禁食影响。bST不影响A1R的Bmax;然而,禁食使Bmax降低了38%。数据突出了bST和禁食对BAR和A1R的差异调节作用。