Effects of constant infusion with insulin-like growth factor-I (IGF-I) to immature female rats on body weight gain, tissue growth, and sexual function - Evidence that such treatment does not affect sexual maturation or fertility

被引:16
作者
Gruaz, NM
dAlleves, V
Charnay, Y
Skottner, A
Ekvarn, S
Fryklund, L
Aubert, ML
机构
[1] UNIV GENEVA,SCH MED,DEPT PEDIAT,DIV BIOL GROWTH & REPROD,CH-1211 GENEVA,SWITZERLAND
[2] UNIV GENEVA,SCH MED,DEPT PSYCHIAT,DIV NEUROPSYCHIAT,CH-1211 GENEVA,SWITZERLAND
[3] PHARMACIA & UPJOHN INC,STOCKHOLM,SWEDEN
关键词
sexual maturation; puberty; insulin-like growth factor-I (IGF-I); insulin-like growth factor binding proteins (IGFBPs); gonadotropin-releasing hormone (GnRH); ovary; fertility; female rats;
D O I
10.1007/BF02738796
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Plasma levels for insulin-like growth factor-1 (IGF-I) steadily increase in female rats between 20 and 40 d of life, and this increase is intimately related to the well-known growth spurt occurring at this age. Since specific actions of IGF-I related to sexual function have been described at the ovarian and hypothalamic levels, an endocrine role of rising circulating IGF-I levels during sexual maturation cannot be excluded. Therefore, the impact of adult-type plasma IGF-I levels during the juvenile age, on body weight (BW) gain, growth of several organs, sexual development, and fertility has been evaluated. Female Sprague-Dawley rats were infused with rhIGF-I (2 and 4 mu g/g BW/d, using Alzet minipumps), between 20 and 41 d of life. When infusing 2 mu g/g BW/d, plasma levels for IGF-I were increased 1.5- to 2-fold over controls at all ages studied. They were further increased with the higher dosage, but only after 35 d of age. Plasma levels for insulin-like growth factor binding protein (IGFBP)-1 to -3 were clearly increased. BW gain was significantly increased, but only with the higher dosage. Tail length was never modified. In contrast, a growth acceleration for spleen, kidneys, adrenals, and ovaries was observed with both dosages. The ovarian weight of treated animals represented approx 140% of control animals with the 4 mu g/g BW/d dosage. Histology of the enlarged ovaries did not reveal any abnormalities. No meaningful modification of the timing of vaginal opening was observed, and fertility was not compromised by previous rhIGF-I infusion during the 20-41 d age period. In summary, early exposure to increased (adult-like) plasma IGF-I levels did not modify BW gain or tail length, but affected the development of spleen, kidneys, adrenals, and ovaries. Exposure to supraphysiological plasma IGF-I levels (>1200 ng/mL), accelerated BW gain and increased the weight of all organs studied. No signs of precocious sexual maturation were seen and fertility was normal. In conclusion, prematurely increased plasma IGF-I levels affected somatotropic parameters, but not the onset of sexual function.
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页码:11 / 19
页数:9
相关论文
共 42 条
[1]   FOLLICLE-STIMULATING-HORMONE INHIBITS THE CONSTITUTIVE RELEASE OF INSULIN-LIKE GROWTH-FACTOR BINDING-PROTEINS BY CULTURED RAT OVARIAN GRANULOSA-CELLS [J].
ADASHI, EY ;
RESNICK, CE ;
HERNANDEZ, ER ;
HURWITZ, A ;
ROSENFELD, RG .
ENDOCRINOLOGY, 1990, 126 (02) :1305-1307
[2]   INSULIN-LIKE GROWTH-FACTORS AS INTRAOVARIAN REGULATORS OF GRANULOSA-CELL GROWTH AND FUNCTION [J].
ADASHI, EY ;
RESNICK, CE ;
DERCOLE, AJ ;
SVOBODA, ME ;
VANWYK, JJ .
ENDOCRINE REVIEWS, 1985, 6 (03) :400-420
[3]   PLASMA GROWTH-HORMONE (GH) RESPONSE TO INTRAVENOUS GH-RELEASING FACTOR (GRF) IN ADULT-RATS - EVIDENCE FOR TRANSIENT PITUITARY DESENSITIZATION AFTER GRF STIMULATION [J].
ARSENIJEVIC, Y ;
RIVEST, RW ;
ESHKOL, A ;
SIZONENKO, PC ;
AUBERT, ML .
ENDOCRINOLOGY, 1987, 121 (04) :1487-1496
[4]   REGULATION OF INSULIN-LIKE GROWTH-FACTOR BINDING PROTEIN-3 MESSENGER-RIBONUCLEIC-ACID EXPRESSION BY INSULIN-LIKE GROWTH FACTOR-I [J].
BALE, LK ;
CONOVER, CA .
ENDOCRINOLOGY, 1992, 131 (02) :608-614
[5]  
Baxter R C, 1989, Prog Growth Factor Res, V1, P49, DOI 10.1016/0955-2235(89)90041-0
[6]   EXPRESSION OF INSULIN-LIKE GROWTH FACTOR-I STIMULATES NORMAL SOMATIC GROWTH IN GROWTH HORMONE-DEFICIENT TRANSGENIC MICE [J].
BEHRINGER, RR ;
LEWIN, TM ;
QUAIFE, CJ ;
PALMITER, RD ;
BRINSTER, RL ;
DERCOLE, AJ .
ENDOCRINOLOGY, 1990, 127 (03) :1033-1040
[7]   SOMATOMEDIN-C MEDIATES GROWTH-HORMONE NEGATIVE FEEDBACK BY EFFECTS ON BOTH THE HYPOTHALAMUS AND THE PITUITARY [J].
BERELOWITZ, M ;
SZABO, M ;
FROHMAN, LA ;
FIRESTONE, S ;
CHU, L ;
HINTZ, RL .
SCIENCE, 1981, 212 (4500) :1279-1281
[8]   ACUTE SUPPRESSION OF GONADOTROPIN-RELEASING-HORMONE SECRETION BY INSULIN-LIKE GROWTH FACTOR-I AND SUBPRODUCTS - AN AGE-DEPENDENT ENDOCRINE EFFECT [J].
BOURGUIGNON, JP ;
GERARD, A ;
GONZALEZ, MLA ;
FRANCHIMONT, P .
NEUROENDOCRINOLOGY, 1993, 58 (05) :525-530
[9]  
BRAZEAU P, 1982, CR ACAD SCI III-VIE, V295, P651
[10]   RADIOIMMUNOASSAY FOR INSULIN-LIKE GROWTH FACTOR-I - SOLUTIONS TO SOME POTENTIAL PROBLEMS AND PITFALLS [J].
BREIER, BH ;
GALLAHER, BW ;
GLUCKMAN, PD .
JOURNAL OF ENDOCRINOLOGY, 1991, 128 (03) :347-357