Yu W H, Kimura M, Walczewska A, Karanth S, McCann S M
Pennington Biomedical Research Center, Louisiana State University, Baton Rouge 70808-4124, USA.
Proc Natl Acad Sci U S A. 1997 Feb 4;94(3):1023-8. doi: 10.1073/pnas.94.3.1023.
A defect in the structure of the obese gene is responsible for development of obesity in the ob/ob mouse. The product of expression of the gene is the protein hormone leptin. Leptin causes weight loss in ob/ob and normal mice, it is secreted by adipocytes, and it is an important controller of the size of fat stores by inhibiting appetite. The ob/ob mouse is infertile and has a pattern of gonadotropin secretion similar to that of prepubertal animals. Consequently, we hypothesized that leptin might play a role in the control of gonadotropin secretion and initiated studies on its possible acute effects on hypothalamic-pituitary function. After a preincubation period, hemi-anterior pituitaries of adult male rats were incubated with leptin for 3 hr. Leptin produced a dose-related increase in follicle-stimulating hormone (FSH) and luteinizing hormone (LH) release, which reached peaks with 10(-9) and 10(-11) M leptin, respectively. Gonadotropin release decreased at higher concentrations of leptin to values indistinguishable from that of control pituitaries. On the other hand, prolactin secretion was greatly increased in a dose-related manner but only with leptin concentrations (10(-7)-10(-5) M). Incubation with leptin of median eminence-arcuate nuclear explants from the same animals produced significant increases in LH-releasing hormone (LHRH) release only at the lowest concentrations tested (10(-12)-10(-10) M). As the leptin concentration was increased, LHRH release decreased and was significantly less than control release at the highest concentration tested (10(-6) M). To determine if leptin can also release gonadotropins in vivo, ovariectomized females bearing implanted third ventricle cannulae were injected with 10 microg of estradiol benzoate s.c., followed 72 hr later by microinjection into the third ventricle of leptin (0.6 nmol in 5 microl) or an equal volume of diluent. There was a highly significant increase in plasma LH, which peaked 10-50 min after injection of leptin. Leptin had no effect on plasma FSH concentrations, and the diluent had no effect on either plasma FSH or LH. Thus, leptin at very low concentrations stimulated LHRH release from hypothalamic explants and FSH and LH release from anterior pituitaries of adult male rats in vitro and released LH, but not FSH, in vivo. The results indicate that leptin plays an important role in controlling gonadotropin secretion by stimulatory hypothalamic and pituitary actions.
肥胖基因结构的缺陷导致ob/ob小鼠发生肥胖。该基因表达的产物是蛋白质激素瘦素。瘦素可使ob/ob小鼠和正常小鼠体重减轻,它由脂肪细胞分泌,通过抑制食欲来控制脂肪储备的大小,是脂肪储备大小的重要调节因子。ob/ob小鼠不育,其促性腺激素分泌模式与青春期前动物相似。因此,我们推测瘦素可能在促性腺激素分泌的控制中发挥作用,并开始研究其对下丘脑 - 垂体功能可能的急性影响。在预孵育期后,将成年雄性大鼠的半前脑垂体与瘦素一起孵育3小时。瘦素使促卵泡激素(FSH)和促黄体生成素(LH)的释放呈剂量依赖性增加,分别在瘦素浓度为10^(-9)和10^(-11) M时达到峰值。在更高浓度的瘦素作用下,促性腺激素释放减少至与对照垂体无差异的值。另一方面,催乳素分泌仅在瘦素浓度为10^(-7) - 10^(-5) M时以剂量依赖性方式大幅增加。用来自相同动物的正中隆起 - 弓状核外植体与瘦素孵育,仅在测试的最低浓度(10^(-12) - 10^(-10) M)下促黄体生成素释放激素(LHRH)释放显著增加。随着瘦素浓度增加,LHRH释放减少,在测试的最高浓度(10^(-6) M)时显著低于对照释放。为了确定瘦素在体内是否也能释放促性腺激素,给植入第三脑室套管的去卵巢雌性大鼠皮下注射10μg苯甲酸雌二醇,72小时后向第三脑室内微量注射瘦素(0.6 nmol溶于5μl)或等体积的稀释剂。注射瘦素后血浆LH高度显著增加,在注射后10 - 50分钟达到峰值。瘦素对血浆FSH浓度无影响,稀释剂对血浆FSH或LH均无影响。因此,极低浓度的瘦素在体外刺激下丘脑外植体释放LHRH以及成年雄性大鼠前脑垂体释放FSH和LH,在体内释放LH,但不释放FSH。结果表明,瘦素通过刺激下丘脑和垂体发挥作用,在控制促性腺激素分泌中起重要作用。