Oscar T P
USDA, Agricultural Research Service, Princess Anne, Maryland 21853, USA.
Poult Sci. 1996 Aug;75(8):1027-34. doi: 10.3382/ps.0751027.
A radioreceptor assay that specifically measures the affinity and concentration of glucagon receptors on the surface of broiler adipocytes was used to determine whether down-regulation of glucagon receptors is involved in the mechanism whereby glucagon induces desensitization of its ability to acutely stimulate lipolysis. Adipocytes from abdominal fat of 42- to 49-d-old female broilers were preincubated in vitro with 0 to 8 nM glucagon for 0 to 24 h before removal of glucagon by washing and assessment of lipolysis during a subsequent 1 h incubation at 37 C and binding of ([125I]iodo-Tyr10) glucagon during an ensuring 6 h incubation at 12 C. In Experiment 1, pretreatment of adipocytes with 0 to 8 nM glucagon for 24 h reduced lipolysis 70% with a preincubation dose of glucagon (ED50) of 0.4 +/- 0.04 nM, whereas glucagon binding was decreased 75% with an ED50 of 0.7 +/- 0.1 nM. In Experiment 2, pretreatment of adipocytes with 5.4 nM glucagon for 0 to 2 h decreased lipolysis 60% with a time of preincubation with glucagon (T1/2) of < 1 min, whereas glucagon binding was reduced 40% with a T1/2 of 2 +/- 0.6 min. In Experiment 3, detailed analysis of lipolysis and glucagon binding to adipocytes pretreated with 5.4 nM glucagon for 5 min, 2 h, or 24 h revealed that sensitivity of adipocytes to acute stimulation of lipolysis by glucagon and the number of glucagon receptors on the adipocyte surface were decreased by glucagon pretreatment. The assay concentration of glucagon (EC50) for glucagon stimulation of lipolysis, a measure of adipocyte sensitivity, increased 0.8-fold at 5 min, 1.6-fold at 2 h, and 4.9-fold at 24 h of preincubation. The number of low-affinity glucagon receptors decreased 12% at 5 min, 20% at 2 h, and 50% at 24 h of preincubation with glucagon. Throughout this study, decreased glucagon binding was closely associated with reduced lipolysis, implicating down-regulation of cell-surface glucagon receptors in the mechanism whereby glucagon induces desensitization of its ability to acutely stimulate lipolysis in broiler adipocytes.
采用一种特异性测定肉鸡脂肪细胞表面胰高血糖素受体亲和力和浓度的放射受体分析法,来确定胰高血糖素受体下调是否参与了胰高血糖素诱导其急性刺激脂肪分解能力脱敏的机制。将42至49日龄雌性肉鸡腹部脂肪的脂肪细胞在体外与0至8 nM胰高血糖素预孵育0至24小时,然后通过洗涤去除胰高血糖素,并在随后37℃孵育1小时期间评估脂肪分解情况,以及在接下来12℃孵育6小时期间评估([125I]碘-Tyr10)胰高血糖素的结合情况。在实验1中,用0至8 nM胰高血糖素对脂肪细胞进行24小时预处理,使脂肪分解减少70%,胰高血糖素预孵育剂量(ED50)为0.4±0.04 nM,而胰高血糖素结合减少75%,ED50为0.7±0.1 nM。在实验2中,用5.4 nM胰高血糖素对脂肪细胞进行0至2小时预处理,使脂肪分解减少60%,胰高血糖素预孵育时间(T1/2)<1分钟,而胰高血糖素结合减少40%,T1/2为2±0.6分钟。在实验3中,对用5.4 nM胰高血糖素预处理5分钟、2小时或24小时的脂肪细胞的脂肪分解和胰高血糖素结合进行详细分析,结果显示胰高血糖素预处理降低了脂肪细胞对胰高血糖素急性刺激脂肪分解的敏感性以及脂肪细胞表面胰高血糖素受体的数量。胰高血糖素刺激脂肪分解的测定浓度(EC50),即脂肪细胞敏感性的指标,在预孵育5分钟时增加0.8倍,2小时时增加1.6倍,24小时时增加4.9倍。与胰高血糖素预孵育5分钟时,低亲和力胰高血糖素受体数量减少12%,2小时时减少20%,24小时时减少50%。在整个研究过程中,胰高血糖素结合减少与脂肪分解减少密切相关,这表明细胞表面胰高血糖素受体下调参与了胰高血糖素诱导肉鸡脂肪细胞急性刺激脂肪分解能力脱敏的机制。