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PubMed1993

Evidence that neuropeptide Y could represent a neuroendocrine inhibitor of sexual maturation in unfavorable metabolic conditions in the rat.

Neuropeptide Y (NPY) is known to be involved in the central regulation of appetite, sexual behavior and reproductive function. Whereas central administration of NPY strongly stimulates feeding, diet restriction produces overexpression of NPY in the arcuate and paraventricular nuclei that might reflect behavioral adaptations to shortage of food. The role of NPY for the regulation of sexual function is still controversial. Whereas NPY is stimulatory during proestrus in the rat, acute administration of NPY is inhibitory in castrated animals and we have shown that chronic administration of NPY inhibits both the gonadotropic and somatotropic axis in adult female rats. In order to further analyse the role of NPY during sexual maturation, a model of delayed sexual maturation imposed by food restriction and return to ad-libitum feeding was used. Young female rats were restricted to 7-8 g food daily starting at 24 days of life (d). This restriction completely prevented sexual maturation. At 50 d, ICV cannulas were placed and at 60 d, Alzet minipumps either delivering NPY (18 micrograms/day) or vehicle into the ICV cannula were implanted dorsally. At 61 d, rats were switched to ad-libitum feeding, a change that produced vaginal opening within 4 days in all vehicle-treated rats. In the rats receiving NPY, significantly increased food intake and weight gain were observed but only one out of the 9 rats studied experienced vaginal opening at 66 d, the other 8 animals remaining sexually immature at 67 d at sacrifice. Sexual immaturity of NPY-treated rats was further confirmed by decreased ovarian weight and reduced number of pituitary GnRH receptors. Plasma IGF-I levels were markedly reduced in NPY-treated rats. Since food restriction has been shown both to increase hypothalamic NPY and to reduce or inhibit sexual function, these data bring evidence for the first time that NPY could be involved in the inhibition of sexual maturation imposed by food restriction, since maintenance of elevated NPY levels in the hypothalamus did prolong this state of sexual immaturity despite restoration of normal food intake.

Animals↗

PubMed1985

Bromoergocryptine decreases serum prolactin and delays sexual maturation in male golden hamsters.

The role of prolactin during sexual maturation in male golden hamsters was studied. Controls (n = 23) received vehicle and treated animals (n = 23) received 500 micrograms 2-bromo-alpha-ergocryptine (CB154) daily from 10 days of age until 4 or 5 wk of age. Serum prolactin in prepubertal male hamsters was reduced to a nondetectable level by treatment with the dopamine agonist CB154. Flank gland diameter, body weight, testicular and total accessory sex organ weights, and serum testosterone were all significantly lower (P less than 0.05) in the CB154-treated animals. In addition, seminiferous tubule area, seminiferous tubule luminal and cellular areas, and number of late spermatids per tubule cross-section were significantly reduced (P less than 0.01) in CB154-treated prepubertal males. Thus, the absence of prolactin retarded sexual maturation in male golden hamsters. These data suggest, that prolactin enhances testosterone production during the process of sexual maturation and supports the development of androgen-dependent tissues.

Aging↗

PubMed1992

Growth and sexual maturation of Brazilian patients with sickle cell diseases.

Growth and sexual maturation was studied of 125 Brazilian patients with sickle cell disease whose ages ranged from 7 months to 42 years. Height and weight were significantly lower when compared with the unaffected population. The height and weight deficit increased in the age range of 11-19 years as compared with patients less than 11 years of age. Age of menarche, breast and pubic hair staging in girls, and genitalia staging and testicular volume measurements in boys indicated a delayed sexual maturation for both sexes. The comparison of adult and young patients, however, demonstrated that although puberty is delayed, a normal sexual maturation is attained later in life by most patients.

Adolescent↗

PubMed1995

Chronic administration of neuropeptide Y into the lateral ventricle starting at 30 days of life delays sexual maturation in the female rat.

The role of neuropeptide Y (NPY) in the regulation of sexual function is still controversial. Whereas central NPY administration is stimulatory during proestrus in the rat and other species, such administration is inhibitory in castrated animals and we have shown that chronic, central infusion of NPY inhibits both the gonadotropic and somatotropic axis in adult rats. Previous studies have suggested that NPY could be involved in the triggering of the first ovulatory LH surge and a recent report indicated that a single central NPY injection given at 30 days of life could advance sexual maturation. We therefore evaluated the effect of chronic NPY administration on the timing of sexual maturation in the female rat and compared the effects obtained with those induced by a single NPY injection. Constant infusion of NPY (18 micrograms/day) into the lateral ventricle delayed sexual maturation as seen by the absence of vaginal opening, delayed ovarian growth and reduced number of pituitary GnRH receptors. This inhibitory effect was seen as long as NPY was infused. In contrast, a single NPY injection either at 30 days of life or earlier, or repeated single injections between 28 and 31 days of life, did not modify the pace of sexual maturation. Unlike what is observed in adult animals, overall food intake was only minimally increased between 30 and 37 days of life in chronically NPY-infused rats, but this increase became more important thereafter.(ABSTRACT TRUNCATED AT 250 WORDS)

Amino Acid Sequence↗

PubMedDate not supplied

Proteolytic cleavage of ACTH in corticotropes of sexually mature axolotls (Ambystoma mexicanum).

Immunohistochemical analysis of the pituitary of sexually mature axolotls revealed both ACTH(1-39)-related and alpha-MSH-related immunoreactivity present in corticotropic cells located in the rostral anterior pituitary. Gel filtration analysis indicated that the ACTH(1-39)-sized immunoreactivity and the alpha-MSH-sized immunoreactivity detected in acid extracts of the axolotl anterior pituitary were present in a ratio in a range between 1:1 and 1:0.6. Reversed-phase HPLC analyses indicated that the alpha-MSH-sized immunoreactivity had the same retention time as synthetic ACTH(1-13)-NH2. The corticotropic activity of the ACTH(1-39)-sized immunoreactivity and the purified ACTH(1-13)-NH2 was tested in a heterologous, larval bullfrog adrenal bioassay system. As expected, the ACTH(1-39)-sized immunoreactivity stimulated corticosterone release; however, the purified ACTH(1-13)-NH2 lacked glucocorticoid activity. The proteolytic cleavage of ACTH in corticotropes of sexually mature axolotls was identical to the cleavage events observed in neotenic Ambystoma tigrinum that had not reached sexual maturity. These studies indicate that the transient expression of ACTH cleavage activity is not affected by the reproductive state of the animal. Since axolotls do not undergo metamorphosis, it is possible that events associated with metamorphosis may induce the decline in ACTH cleavage activity observed in amphibian corticotropes.

Adrenal Cortex↗

PubMed1976

Ovarian control of gonadotropin secretion during induced precocious sexual maturation in the rat.

In sexually immature female rats 'primed' with a unilateral basal hypothalamic lesion on day 23 of life, a gonadotropin surge was triggered by progesterone (P) on day 26. The influence of sequential ovariectomy (OVX) on this response was studied in an attempt to elucidate the mode of action of brain lesions inducing precocious sexual maturation in this species. OVX, carried out on days 23-26, abolished or greatly reduced the LH surge, but had little effect on basal LH concentrations. In contrast, basal FSH concentrations rose rapidly after OVX. In lesioned rats, the post-castration rise of FSH could be prevented by leaving the ovaries in place during the 1st 24 or 48 h. It is concluded that the lesion-induced maturation of the positive feedback mechanism underlying the pubertal preovulatory gonadotropin surge is mediated by the ovaries. In prepubertal rats at this age, tonic FSH release, but not tonic LH release, is under tight negative feedback control.

Animals↗

PubMed1978

Sexual maturity in broiler breeder males.

Sexual maturity and fertility of two lines of broiler breeder males, one commercial and one experimental, were evaluated individually in order to determine the earliest age at which they could be expected to produce viable spermatozoa capable of producing acceptable fertility. Comparative data for the two lines were also collected on duration of fertility, percent fertility, percent hatchability and chicks per hen during an 8-week period using pooled semen from each of the two lines. The results of this study indicate that 9.1 and 6.8% of the male of the experimental and commercial lines, respectively, produce viable spermatozoa at 11 weeks of age, and consequently, could be selected at that age and used to reproduce stock under selection. The duration of fertility was 10.5 days for the experimental line and 8.8 days for the commercial lines; with fertility levels of 86.1 and 82.8%, respectively, for the eggs produced by the two lines during this period. There were no differences in fertility, hatchability, or chicks produce per hen between the two lines for the 8-week reproductive period.

Age Factors↗

PubMed1990

Zinc, copper, and sexual maturation in 9-18-year-old girls and boys.

The relationships between serum levels of zinc and copper and sexual maturation were analyzed in 2291 9-18-yr-old Finnish girls and boys. Development of public hair, breasts, and genitalia were used to grade maturation according to Tanner's classification. Serum zinc and sexual maturation were not related. However, 15- and 18-yr-old girls who had matured most slowly had low serum levels of zinc compared with their age mates. Thus, sexual maturation seems not to be affected by zinc deficiency in Finland; effects of zinc status on maturation in some minor groups cannot, however, be excluded. Serum copper levels were associated with age and sexual maturation, which complicates the drawing of conclusions about possible deficiencies.

Adolescent↗

PubMed1985

Inhibitory action of exogenous melatonin, 5-methoxytryptamine, and 6-hydroxymelatonin on sexual maturation of male rats: activity of 5-methoxytryptamine might be due to its conversion to melatonin.

The effect on sexual maturation of 6 different pineal indoles, including melatonin, and of the metabolite 6-hydroxymelatonin was studied in the male rat after daily injections from 20 to 40 days of age. Only 5-methoxytryptamine (5MT) and 6-hydroxymelatonin (6M), in addition to melatonin, inhibited the neuroendocrine-reproductive axis during sexual maturation. Their potencies when injected in the afternoon were in the range of one-twentieth to one-fifth that of melatonin. Like melatonin these two indoles had no effect when injected in the morning. N-acetylserotonin, serotonin, 5-hydroxytryptophol and 5-methoxytryptophol did not influence sexual maturation either when injected in the morning or in the afternoon. Chromatographic separation was performed on plasma extracts from rats injected daily with the biologically active indoles and killed 10-120 min after the last injection. This procedure confirmed that 6M injections did not increase plasma melatonin levels. In contrast, plasma melatonin levels in 5MT-treated rats were increased 1 h after the 5MT injection. These results suggest that 5MT or part of it might be acetylated to melatonin; thus inhibition of sexual maturation might be mainly due to melatonin. These results indirectly support the contention that melatonin is the principal pineal indoleamine playing a role during sexual maturation.

5-Methoxytryptamine↗

PubMed1990

Accumulation of cardiac lipofuscin in mammals: correlation between sexual maturation and the first appearance of lipofuscin.

Accumulation of lipofuscin is an important phenomenon of the cellular aging process. The first appearance of cardiac lipofuscin showed a good correlation with sexual maturation, which was correlated with maximum life-span of mammals. Large metabolic changes occurred at sexual maturation. From these results, it is suggested that sexual maturation of mammals is the initiation period of the aging process. Correlation between sexual maturation and longevity was re-evaluated using many mammals. Domestic and laboratory animals showed an earlier sexual maturation than other mammals, including rodents.

Aging↗

PubMed2005

Sexual maturation in early adolescence and alcohol drinking and cigarette smoking in late adolescence: a prospective study of 2,129 Norwegian girls and boys.

Early sexual maturation has been associated with higher involvement in risk behaviour during early and mid-adolescence. In a prospective study of 2,129 girls and boys, we investigated whether the timing of sexual maturation was associated with cigarette smoking and alcohol drinking in late adolescence and whether this relation differed between boys and girls. Nine hundred and eighty boys and 1,149 girls, who participated in a cross-sectional study in middle school, were included in a follow-up study in high school 4 years later. Self-rating of pubertal status, as registered at baseline in middle school, was used to indicate the timing of sexual maturation. Age-adjusted odds ratios (ORs) with 95% confidence intervals (CIs), estimated by logistic regression, were used to assess the association between sexual maturation and alcohol drinking and daily smoking at follow-up. We found that girls who had matured early (OR 1.7, CI 1.2-2.4) or late (OR, 1.5, CI, 1.1-2.2) were both more likely to report more advanced drinking in late adolescence than were girls who were on time. Boys who had matured late were less likely (OR 0.5, CI 0.3-0.8) than boys who were on time to engage in advanced drinking. In general, daily smoking was more common among girls than boys, and more common among girls who had matured early (OR 1.5, CI 1.1-2.2) than among girls who were on time. Adjustment for social factors, e.g. parental education and marital status and parental drinking and smoking habits, did not substantially influence these results. We concluded that, for girls, but not for boys, early sexual maturation was associated with more advanced drinking and higher frequency of smoking in late adolescence. In boys, late sexual maturation was associated with reduced risk of advanced drinking.

Adolescent↗

PubMed2003

On the use of the perineal stain as an index of sexual maturity and breeding condition in the male greater cane rat, Thryonomys swinderianus, Temminck.

The efficacy of the perineal stain as an index for sexual maturity and breeding condition in the male greater cane rat, Thryonomys swinderianus, Temminck, was investigated in 34 animals collected from hunters' kills in the Ekumfi District of Ghana, between April and June 1989. The results indicated that, although the presence of the perineal stain was conclusive proof of sexual maturity in an individual, it was not efficacious as an index for sexual maturity for biological work in these animals (p > 0.05) because it excluded some that, although sexual mature, did not exhibit the trait, particularly young adults. However, the perineal stain may be useful as a management tool for identifying sexually mature captive greater cane rats. About 7 out of every 10 caught each month were found to be in breeding condition.

Animals↗

PubMed2005

The testis histology of artificially maturated European eel (Anguilla anguilla L.) at the end of sexual maturation, and spermatozoa ultrastructure in freshwater rearing. Short communication.

The artificial induction of sexual maturation of European eel males was carried out by using weekly hCG administrations. Histological pictures showed that the testis tissues developed and regressed naturally and no pathological changes took place under the conditions of artificial rearing in freshwater. According to light and electron microscopic investigations the morphology and motility of the spermatozoa of males kept in freshwater proved to be similar to those in seawater. The authors suppose that freshwater rearing of males is not a barrier factor in the artificial propagation of European eels.

Anguilla↗

PubMed2003

Effect of selection for growth on onset of sexual maturity in randombred and growth-selected lines of Japanese quail.

An experiment was conducted to determine the effect of selection for growth (BW) on the onset of reproduction (first egg) in Japanese quail hens from growth-selected (HW) and randombred (R1) lines. The HW line had undergone over 40 generations of selection for increased 4-wk BW and was originally developed from the R1 line. Data were collected over two consecutive hatches and summarized by hatch and within lines. Body weight at 35 d of age was positively correlated with BW at sexual maturity (first egg) in both the R1 and HW lines, but these correlations were not significant in both hatches for either line (Hatch 1-R1; Hatch 2-HW; P < or = 0.05). There was a negative correlation between age at sexual maturity (days to first egg) and 35 d BW in both lines with the exception of the HW hens in Hatch 2. Age at sexual maturity and BW at sexual maturity was positively correlated (P < or = 0.001) in the R1 line but did not show the same relationship in the HW line. Age at sexual maturity and weight of the abdominal fat pad were positively correlated in the R1 line (Hatch 1, P < or = 0.01; Hatch 2, P < or = 0.001), but this relationship was not significant in the HW line. Age at sexual maturity and follicle number was negatively correlated in both lines but was not significant in Hatch 2 of the HW line. Follicle size, however, was positively correlated with days to first egg in only Hatch 2 (P < or = 0.001) of the HW line. The data suggest that the relationships between the onset of sexual maturity and both reproductive parameters and carcass traits in hens from consecutive hatches of HW quail are less clear than in the R1 line.

Aging↗

PubMed1988

Effects of treatment with the opioid antagonists naloxone and naltrexone on LH secretion and on sexual maturation in immature female rats.

The effects on sexual maturation of the opioid receptor antagonists naloxone and naltrexone were studied in the female rat. Neonatal treatment (days 1-10) with either naloxone (2.5 mg/kg at 6-h intervals) or naltrexone (20 or 50 mg/kg per day) did not advance sexual maturation as judged by age and body weight at vaginal opening and first ovulation. After treatment with naltrexone (20 mg/kg) first ovulation occurred 2.3 days earlier than in saline-treated control rats but this could be attributed to a growth-stimulating effect of naltrexone; the effect was not observed with 50 mg/kg. An effect of neonatal treatment with naloxone on serum LH levels was seen at 23 days of age (155 +/- 36 (S.E.M.) vs 14 +/- 4 micrograms LH/l in controls, P less than 0.01), but not at 29 or 33 days of age, at 2 days before first ovulation nor at first pro-oestrus. There were no differences in the number of ova released at first oestrus, nor in the length of the first cycle. Neonatal treatment with naltrexone (50 mg/kg per day) did not alter the response to treatment with human chorionic gonadotrophin at 28-31 days of age: ovulation of a mean of 7.3 ova was induced on day 32 in both naltrexone- and saline-treated rats. Naltrexone treatment (four daily injections of 20 mg/kg at 2-h intervals) at 28-32 days of age advanced first ovulation by 4.4 days in about 40% of the rats.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1999

Sex-related influence of body size and sexual maturation on blood pressure in adolescents.

OBJECTIVE: This study is aimed at investigating the influence of body size, body fat and sexual maturation on blood pressure (BP) in adolescents. DESIGN: A cross-sectional study. SETTING: A suburban student population of Southern Italy. SUBJECTS: One hundred ninety students attending the first and second year of a secondary school. Five were excluded because they were affected by major diseases. The remaining were 98 M and 87 F (mean age for either group = 12.0+/-0.8 y). METHODS: Blood pressure was measured by a mercury sphygmomanometer, body weight by a platform beamscale, other measurements included height, biceps, triceps, subscapular and suprailiac skinfolds by a caliper; sexual maturation was evaluated according to Tanner. RESULTS: Body size was greater than in Tanner's population: in particular body weight (but not height) in our sample markedly exceeded that of the children of the same age in Tanner's population. Boys had higher systolic blood pressure (SBP) than girls (BP = 109/64+/-12/10 vs. 103/63+/-11/8 mm Hg, P<0.02 for SBP), while heart rate and waist/hip ratio were lower. During puberty evaluated on the basis of pubic hair growth BP in girls was higher than in the prepubertal phase (107/66+/-9/7 vs. 99/61+/-10/7, P<0.01). Pubertal boys showed a reduced percent of body fat (calculated from four skinfold measurements) in comparison to prepubertal ones (21.0%+/-4.5 vs. 24.5%+/-7.1, P<0.01). In linear correlation analysis, height, BW, BMI and lean body mass were found to be significantly associated with SBP in both sexes and to diastolic blood pressure (DBP) in girls. Percent body fat was correlated with SBP in boys, while sexual maturation was associated to SBP and DBP in girls only. Multiple regression analysis indicated a significant contribution of body size to BP variability, particularly in the girls. Sexual maturation was excluded from the final regression equations when height, BW or lean body mass were present. CONCLUSIONS: These data indicate that body weight in these adolescents is greater that in Tanner's population of the same age and sex. Body size appears to be a major determinant of BP, whereas sexual maturation seems to influence BP levels mainly through body growth. The influence of percent body fat on BP setting seems to be of limited importance.

Adolescent↗

PubMed1987

A study of spontaneous sexual maturation of the female ferret.

Although ferrets are long-day breeders, females reared exclusively in nonstimulatory short days will undergo spontaneous sexual maturation by 30-50 wk of age. In the following report, this spontaneous sexual maturation of ferrets was studied to determine mechanisms regulating sexual maturation in nonstimulatory photoperiods. Study of ovariectomized females treated with low, constant levels of estradiol suggest that a marked decrease in the efficacy of estradiol to inhibit luteinizing hormone secretion occurs shortly before sexual maturity becomes evident in intact controls (both groups housed in short days). During this long juvenile period, a marked increase in body weight occurred, but ovarian responsiveness to exogenous gonadotropin did not change. Older, larger females did respond more rapidly to stimulatory photoperiod than did younger females. These studies suggest that the mechanisms of spontaneous puberty in ferrets are likely the same as those regulating photoperiod-stimulated puberty in this species.

Animals↗

PubMed1998

Ovarian modulation of the oestradiol-induced LH surge in prepubertal and sexually mature gilts.

The role of ovarian secretions in modulating positive oestrogen feedback on LH release in late prepubertal and sexually mature gilts was studied. Gilts were either ovariectomized (OVX) at 230 days of age (sexually mature, OVX 230, control), ovariectomized at 160 days of age (pre-pubertal, OVX 160) or ovariectomized at 160 days of age and given either low, high or very high oestradiol substitution therapy (two or three Silastic implants, 5 or 8 cm in length) from 160 days to 230 days (OVX 160 + 2E5, OVX 160 + 2E8 and OVX 160 + 3E8, respectively). The LH surge responses to three i.m. injections of oestradiol benzoate given at intervals of 12 h (in total 10 micrograms oestradiol benzoate kg-1 bodyweight) were compared at 260 days. An additional group of sexually mature gilts was ovariectomized at 260 days (OVX 260) and challenged with oestradiol benzoate at 360 days. LH surges with peak LH concentrations below pretreatment values (resembling LH responses to oestradiol benzoate in immature gilts) were classified as immature, and those with peak LH concentrations above pretreatment values as mature. LH concentrations before treatment with oestradiol benzoate were reduced (P < 0.05) in OVX 160 + 2E8 and OVX 160 + 3E8 gilts compared with OVX 230 (control). When compared with the control group, the time to LH surge peak was longer in OVX 260 gilts, LH peak amplitude was reduced in the OVX 160 group and the area under the curve of the LH surge (ng LH ml-1 plasma (48 h)-1) was less in all other groups (P < 0.05). Classification of LH surges by mature:immature criteria indicated a high mature:immature ratio in OVX 230 gilts (6/1) and a low ratio in OVX 160 (1/7) and OVX 260 (1/6) gilts. The long-term effect of ovariectomy was partially overcome in the OVX 160 + 2E5 group (mature:immature = 3/3). However, previous exposure to supraphysiological concentrations of oestradiol (as in groups OVX 160 + 2E8 and OVX 160 + 3E8) resulted in a high percentage of animals (66% and 100%, respectively) that did not respond to the oestradiol benzoate challenge with an LH surge. Immediately before oestradiol benzoate administration (30 days after removal of implants) plasma oestradiol concentrations in these two groups were still high (P < 0.05) compared with all other groups. GnRH-induced (0.2 microgram kg-1 bodyweight) LH secretion, evaluated 10 days after treatment with oestradiol benzoate, was depressed (P < 0.05) in OVX 160 + 3E8 gilts, but not affected by age at ovariectomy. We suggest that continuous ovarian secretion is necessary for the final maturation of the LH surge mechanism in late prepubertal gilts and also for maintaining the full functionality of this mechanism in sexually mature gilts. The range over which ovarian oestrogens tune the final maturation of this process appears to be rather narrow; however, other ovarian factors may contribute to the final maturation. Furthermore, continued exposure to supraphysiological concentrations of oestradiol was found to be detrimental to the development of the LH surge mechanism.

Analysis of Variance↗