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Dietary arginine and sexual maturation of the female rat.

The effects of dietary arginine deficiency on sexual maturation were examined in the female rat. Consumption of a diet devoid of arginine since weaning delayed the onset of puberty. Weight at vaginal opening and weight at first estrus were significantly greater in the arginine-deficient rat than in the control rat. Arginine deficiency appeared to have a specific effect on the development of reproductive function since puberty in arginine-deficient animals was delayed more than could be accounted for by impairment of growth. The specific effect of arginine deficiency was also indicated by reduced weights of the reproductive tissues after 15 weeks of experimental feeding when compared with the growth-matched controls. Sexual maturation was also examined in rats fed diets containing graded levels of arginine (1.12, 0.84, 0.56, 0.28 or 0%). Vaginal opening and first estrus were delayed by feeding diets containing 0.28 or 0% arginine. Uncoupling of these two events also occurred in the majority of the rats fed these two diets. In spite of normal timing of puberty, maturing rats fed a diet with 0.56 of 0.84% arginine had reduced ovarian weight and first ovulation rate when compared with rats fed the control diet (1.12% arginine). It is concluded that more than 0.84% dietary arginine was required for growing rats to support normal sexual maturation.

Animals↗

Corticosterone administration to rat pups, but not maternal separation, affects sexual maturation and glucocorticoid receptor immunoreactivity in the testis.

Prenatal stress strongly affects sexual dimorphism of male rats. Much less information is instead available on the effects of postnatal stress on sexual maturation during the so-called stress hyporesponsive period (SHRP). For this reason, we compared corticosterone-treated (CS; 10 mg/kg sc, suspended in sesame oil) or maternally separated pups (MS; 5 h/day in the first week of life) with control rats. Control and MS pups also received sesame oil injections. The effects of these procedures on physical development (body weight and eye opening), sexual maturation [anogenital distance, testis weight, 3beta-hydroxysteroid dehydrogenase/(Delta5-4) (3betaHSD) isomerase activity and time to testis descent] and glucocorticoid receptor (GR) immunoreactivity in the testis were examined. Corticosterone treatment significantly (P<.05) advanced testis descent and increased testis weight and 3betaHSD activity at puberty. In addition, adult CS rats presented higher levels of GR immunoreactivity in testicular tubules when compared to control and MS rats. No differences were found between control and MS rats. On this basis, we propose that the silencing of adrenocortical function during the SHRP could be finalized to preserve sexual maturation from the influence of glucocorticoid effects. As SHRP is unique to rodents, this phenomenon could be related to their successful reproductive strategy.

Animals↗

Anthropometric parameters and sexual maturation in 12- to 15-year-old Estonian boys.

The aims of this study were 1. to fix main sexual maturation signs and anthropometric measurements, and 2. to investigate relations between maturational status and main anthropometric parameters (i.e. skinfolds, girths, lengths, breadths/lengths) in 12-15-year old boys. In total, 361 boys from Tartu, Estonia, were studied. Body height and weight, 9 skinfolds, 13 girths, 8 lengths and 8 breadths/lengths were measured. Pubertal stages were determined according to the criteria described by Tanner (1962). Self-assessment of pubic hair (PH1-PH5) was used. Genital development (G1-G5) was estimated by palpating the left testis and matching the size of wood ovoid of the Prader orchidometer. Finally, boys were asked about oigarche (= age at the first ejaculation of sperm). Most of the measured anthropometric variables were significantly different in boys of different chronological age and sexual maturity groups. By linear discriminant analysis, the safety of separation of the chronological age groups was higher than by sexual maturation variables. Nonlinear discriminant analysis allowed to separate sexual maturity groups by anthropometric variables up to 99% security. It was concluded that though the growth and development of a child is highly individual, on an average the anthropometric characteristics alter very constantly with the increase of age and biological maturation. Our results indicated that there were some significant differences in the anthropometrical parameters depending on the chronological age and biological maturation. Mostly length and breadth/length parameters change during the studied age period in respect to sexual development subgroups of boys. The skinfold thicknesses were not changed or even decreased.

Adolescent↗

Retinal fine structure in the European eel Anguilla anguilla. VIII. Photoreceptors of the sexually mature silver eel stage.

The morphology of the photoreceptors of the sexually mature silver eel has been investigated by electron microscopy and these findings compared with observations made on the photoreceptors of the glass, yellow and sexually immature silver eel stages of the lengthy life cycle of the European eel (Anguilla anguilla). As in previous stages the photoreceptors of the sexually mature silver eel are adequately described as either rods or single cones. The rod: cone ratio at this stage is about 200: 1 which is the highest ratio of any of the stages investigated. Rods and perhaps also cones are capable of photomechanical movements. In the light-adapted stage studied, rod inner segments are the same width in the ellipsoid region as the outer segments but the rod myoid region is much thinner. Rod outer segments in the mature silver eel are slightly longer than that observed in the immature silver eel but remain much the same diameter as in previous stages. Cone outer segments taper distally and are not as wide as the inner segments. Both rods and cones display organelles in the inner segment region indicative of active protein production as it is well established that the inner segment is the synthetic center of these cells. In most cones degenerative changes were noted in the mitochondria of the ellipsoid and in the presence empty vacuoles within their cytoplasm. Cone nuclei are large and vesicular and in the light-adapted state are always located sclerad to the external limiting membrane. Rod nuclei are smaller and more electron dense and located within the outer nuclear layer. Both rods and cones still show both invaginated (ribbon) and superficial synaptic sites. In the sexually mature silver eel, therefore, the rod: cone ratio becomes higher still; the rod outer segments become somewhat longer in length and cone cell degenerative changes are even more widespread.

Anguilla↗

Hypothalamic, pituitary, testicular, and secondary organ functions and interactions during the sexual maturation of the male rat.

Puberty in the male rat is a complex process that involves maturational changes in the hypothalamus, pituitary, testes, and secondary sexual organs and in their interrelationships. During the course of sexual maturation the negative feedback control systems for the gonadotropins become less responsive to testosterone while the testes become more responsive to LH. In the immature rat testosterone can potentiate the effect of LH--RH on pituitary LH release; this response is lost with sexual maturation. LH--RH sensitizes the mature male pituitary glands for subsequent LH--RH administration; this self-priming effect is not present in the immature rat. The responsiveness of the secondary organs to testosterone is also altered with age, as is the relative proportion of testosterone and androstendione secreted by the testes. Experiments designed to prevent or mimic the transition in testicular steroid secretion suggest that it may be a critical component of sexual maturation in the male rat. An elevation in androstendione appears to be capable of delaying the maturation of the LH negative feedback system, the prostate gland, and the LH--RH self-priming effect.

Androstenedione↗

The influence of physical exercise on growth and sexual maturation in young female rats.

This investigation deals with the influence of physical activity on the growth and sexual maturation of weanling female Wistar rats. It involves three groups of rats, namely an intensively trained group (n = 45), a moderately trained group (n = 49) and a nontrained group (n = 49). The trained groups were forced to perform physical exercise from the age of 15 days on, on a treadmill. Within the intensively trained group, exercise was increased by increasing the speed and grade of the treadmill. The exercise of the moderately trained group was held constant. A delay in the day at vulva opening, indicating sexual maturation is seen in the extensively trained group in comparison with the moderately trained and nontrained group. The average body weight at the day of vulva opening is the same in all groups. However, the correlation coefficient between day at vulva opening and body fat mass is not significant. No differences in the body- and tail-length growth can be detected between the groups. A delay in the sexual maturation due to stress can be rejected since the open fields results registrating stress parameters, as obtained from the various groups of animals, are in general not significantly different between the intensively trained and moderately trained as well as nontrained groups. This investigation shows evidence that intensive physical exercise from young age on, causes a delay in sexual maturation, although it has no influence on the body- and tail length growth.

Adipose Tissue↗

Effects of social environment on sexual maturation in female cotton rats (Sigmodon hispidus).

Age at sexual maturation among female cotton rats was measured in a variety of intraspecific social environments. Two experiments were conducted. In Experiment I, female cotton rats attained vaginal perforation and first estrus at younger ages and lighter body masses when paired from weaning with a conspecific juvenile male than when caged alone. In Experiment II, these findings were replicated and extended. Females housed with juvenile males matured at the youngest ages, while those housed alone matured at the oldest ages. Females housed with adult males matured at intermediate ages. Presence of a second juvenile female during maturation was significantly associated with early vaginal opening but not with early first estrus. The results of this study are discussed in context of similar social environmental effects on female sexual maturation that have been identified in other rodent species.

Animals↗

A skeletochronological study of growth, longevity, and age at sexual maturity in a population of Rana latastei (Amphibia, Anura).

Longevity and age at sexual maturity in an Italian population of Rana latastei were studied by skeletochronology performed on the phalanges. Frogs collected in 1998 and 1999 by drift fences and pitfall traps were marked by toe-clipping. After marking, individuals were released and the cut phalanges were processed for skeletochronological analysis. The maximum age so far recorded was 3 years in males and 4 years in females. The smallest male and female that were sexually mature on the basis of histological analysis of the gonads were 36 and 35 mm snout vent length (SVL), respectively. In both sexes, most individuals were estimated to breed shortly after emergence from their first overwintering. Among the European Brown Frogs, Rana latastei appears to be one of the shortest-lived and one of the first to reach sexual maturity.

Animals↗

Exteroceptive factors, sexual maturation and reproduction in the female rat.

Keeping a sexually mature male with a weanling female rat advanced neither the time of vaginal opening nor that of 1st oestrus. In 2 of 3 experiments females kept singly after weanling reached sexual maturity significantly earlier than did grouped females. The reproductive performance of females mated at 1st oestrus was not significantly different from that of older primiparae. 26 rats gave birth to an average of 9.3 young at 59.5 days of age, and 22 of them reared 96% of the young to weaning.

Animals↗

Urogastrone-epidermal growth factor and aspects of sexual maturation in female rats as a function of age at treatment.

The effect of epidermal growth factor (EGF) on sexual maturation of female rats was studied. A within-litter experimental design was employed, so that in each litter each female received four daily injections of EGF (E, 500 ng/g body weight s.c.) or vehicle (V), at one of three ages: days 0-3 (E1, V1), days 8-11 (E2, V2), days 16-19 (E3, V3). Body weight, pinna detachment, incisor eruption, eye opening, auditory startle, visual placing, vaginal opening and first cytological oestrus were assessed. Neonatal treatment with EGF (E1) delayed pinna detachment and the appearance of the auditory startle, but accelerated eye opening. Also, E1, but not E2 and E3, resulted in lower body weight at weaning. Treatment E3 advanced sexual maturation, as indicated by vaginal opening and first cytological oestrus, by 5-6 days. E1 and E2 had no such effect. Hence the sensitive period for the effect of EGF on female rat sexual maturation is later than that for effects on other developmental characteristics and body weight. In a second experiment, ovary and uterus weights were found not to differ between E3 and V3 females killed on the day of vaginal opening of the E3 rats, suggesting that the effect of EGF may be specifically on the perineal epithelium and not on sexual maturation generally.

Age Factors↗

[Observations on the acceleration of the sexual maturation of female mice by the presence of males and by exogenous oestrogen (author's transl)].

The influence of the presence of adult males on the acceleration of sexual maturation of female mice was examined under various experimental conditions and compared with the influence of exogenous oestrogen. The criteria of sexual maturation were not equally influenced. It is concluded that sexual maturation is a complex feature and that acceleration of single criteria does not signify sexual maturation.

Animals↗

[Clinical assessment of sexual maturation in adolescents]

OBJECTIVE: To present the methods for clinical evaluation of sexual maturation in adolescents. METHODS: Bibliographic review concerning the practice of pubertal staging. RESULTS: The assessment of sexual maturation is an essential step in the comprehensive health care of adolescents, allowing for the evaluation of their developmental stage. In addition, this assessment allows establishing a correlation between different pubertal events, following up diseases, and interpreting laboratory tests appropriately. Pubertal stage is assessed by the examination of breasts and pubic hair in females, and genitals and pubic hair in males. A new photographic standard for pubertal staging and a new method for clinical measurement of testicular volume are presented. CONCLUSIONS: The assessment of sexual maturation is an important feature in the health care of adolescent patients and must be included in the clinical practice of pediatricians involved in adolescent medicine.

Journal Article↗

Carbohydrate relations during propagation of cuttings from sexually mature Pinus banksiana trees.

Concentrations of glucose, sucrose, soluble reducing sugars, starch and total non-structural carbohydrate were determined during propagation of cuttings from sexually mature Pinus banksiana Lamb. trees. Such cuttings rarely initiate adventitious roots whatever the method or duration of propagation. Terminals, needles, and upper and basal stem segments of cuttings were analyzed at Day 0 and every 2 days for 18 days. Comparison of the results with those of earlier studies with cuttings of P. banksiana seedlings, which root readily, indicated pronounced differences in carbohydrate concentrations and partitioning between the two types of cutting. Compared with those from seedlings, cuttings from sexually mature trees exhibited: (1) more total non-structural carbohydrate in each tissue at Day 0; (2) decreasing rather than increasing total carbohydrate (mainly starch) concentrations in each tissue during propagation; (3) different carbohydrate concentration ratios in each tissue during propagation; and (4) higher sucrose concentrations in terminals during propagation, relative to concentrations at Day 0. Cuttings from sexually mature trees also differed from cuttings of seedlings in having a much lower rate of dry matter accumulation during propagation. These findings suggest that the poor rooting ability of cuttings from sexually mature P. banksiana is not attributable to a lack of total carbohydrate, but that the rooting abilities of cuttings from seedlings and from sexually mature trees differ because of differences between the two types of cutting in rates of net photosynthesis and starch metabolism. The difference in starch metabolism becomes apparent during the first 2 days of propagation.

Journal Article↗

Short-term and long-term effects of melatonin on GnRH-stimulated gonadotropin secretion in pituitaries of sexually maturing rats.

Melatonin administration has been shown to delay sexual maturation in male rats, through an action which involves decreased binding of gonadotropin-releasing hormone (GnRH) in the pituitary and lower pituitary gonadotropin contents. It has been suggested that melatonin must act at a level higher than the pituitary to provoke these effects, but a direct action of melatonin on the pituitary has not been excluded. Using a cell culture system, the gonadotroph responsiveness to GnRH was studied. Pituitaries were obtained either from rats chronically treated with melatonin and showing delayed sexual maturation, or from control rats. In vitro luteinizing hormone and follicle-stimulating hormone response to GnRH was significantly lower when pituitaries were obtained from melatonin-treated rats. However, this diminished response was directly proportional to the amount of gonadotropin contents in cells, so that relative responsiveness, calculated as the amount of gonadotropins released in relation to the gonadotropin content was similar in cells from control and melatonin-treated rats. It is concluded that the effect of melatonin on the pituitary of male rats results from a decrease of gonadotroph growth or gonadotropin synthesis, as a consequence of a change located at the hypothalamic rather than at the pituitary level. This conclusion is further supported by results showing that melatonin added directly in culture medium prior to GnRH does not modify the pituitary responsiveness to GnRH.

Aging↗

Growth and sexual maturation in children with insulin-dependent diabetes mellitus.

Prediabetes, the interval preceding the clinical recognition of diabetes mellitus, is believed to consist of several months or years of beta-cell destruction associated with no clinically recognized signs other than possible increased growth velocity. This increased growth rate may be the result of increased insulin, increased growth hormone, or both. As insulin-dependent diabetes approaches clinical recognition, insulin deficiency becomes manifest as slowing of growth velocity and more obvious weight loss. If a prepubertal child has insulin-dependent diabetes mellitus, sexual maturation is frequently delayed and physical growth is adversely affected. Insulin is an anabolic hormone that regulates metabolic pathways involved in the production of protein, glycogen, and fat. The normal release of growth hormone and the hepatic production of insulin-like growth factor I is modulated by the action of insulin. The absence of physiologic insulin response leads to dysfunctional quantities of growth hormone, insulin-like growth factor I, and sex hormones, resulting in growth impairment and delayed sexual maturation. Delayed sexual maturation may cause concern because it has a major impact on growth and maturation of children. However, there is evidence that sex hormones have a stimulating effect on the tissue damage associated with chronic hyperglycemia. The loss of physiologic insulin release significantly affects physical growth, sexual maturation, and the chronic complications associated with insulin-dependent diabetes mellitus.

Adolescent↗

Luteinizing hormone during sexual maturation in pony mares.

Luteinizing hormone (LH) was quantified in pony mares during artificially induced sexual maturation. Ovarian follicular development was also assessed by rectal palpation of the ovaries. With the exception of large periovulatory LH concentrations in two mares that ovulated, LH concentrations were not significantly different in mares undergoing sexual maturation and thus having marked follicular development when compared with mares that were not undergoing sexual maturation and thus did not have marked follicular development. These results indicate a dissociation in time between the onset of follicular development and the increase in LH which is associated with the first ovulation of the year.

Animals↗

Sexual maturation in underfed weight-matched rats. A test of the "critical body weight" theory of pubertal timing in males.

A popular current theory proposes that the timing of puberty is related to attainment of a critical level of body weight or body fatness. These critical body weight and critical body fat theories have been studied almost exclusively in females. To explore these theories in males, we tested a corollary of these hypotheses: are male rats of the same weight all at the same level of sexual maturation irrespective of prior growth rate? Male rats growing in body weight at five different rates due to various degrees of underfeeding (beginning at weaning) were sacrificed at body weight milestones of 123 and 279 grams. At the first weight milestone, significant (P less than 0.01) inverse correlations were observed among these weight-matched rats between the preceding rate of body weight growth and prostate weight, seminal vesicle weight, testis weight, serum testosterone, and daily sperm production rate, indicating that the underfed animals were more sexually mature. Testis histology also showed that spermatogenic development increased progressively as the prior rate of body weight growth was reduced. These parameters of sexual maturation tended to correlate inversely with body fatness (i.e., leaner animals were more sexually mature) and directly with body length (i.e., longer animals were more sexually mature). By the second body weight milestone, however, the degree of prior underfeeding exerted little effect on those indices of sexual development. We conclude that the degree of sexual maturation in weight-matched animals with varying previous patterns of body weight growth correlates inversely with body fatness and the rate of body weight growth but correlates directly with body length.(ABSTRACT TRUNCATED AT 250 WORDS)

Adipose Tissue↗

Mitochondrial protein synthesis in rainbow trout (Oncorhynchus mykiss) heart is enhanced in sexually mature males but impaired by low temperature

Throughout the life cycle of the rainbow trout (Oncorhynchus mykiss), the heart exhibits periods of enhanced growth. Two such instances are cardiac enlargement associated with sexual maturity in males and heart growth at seasonally low environmental temperatures. Heart growth includes a parallel increase in the number of mitochondria. These natural models of heart growth have been exploited to study protein synthesis directed by the mitochondrial genome. Methods were developed to assess protein synthesis in mitochondria isolated from the heart of rainbow trout. Protein synthesis was assessed by tracking the incorporation of l-[2,6-(3)H]phenylalanine into trichloracetic-acid-precipitable protein. Amino acid incorporation into mitochondrial protein was linear with respect to time and was inhibited by chloramphenicol. Radiolabel was selectively enhanced in molecular mass fractions over the same size range as polypeptides known to be encoded by the mitochondrial genome. Protein synthesis was measured in mitochondria isolated from sexually mature animals and from animals subjected to different thermal regimes. The relative ventricular mass of sexually mature male rainbow trout was significantly greater than that of sexually mature females (0. 104+/-0.004 versus 0.087+/-0.002; mean +/- s.e.m.). Mitochondria isolated from the heart of males synthesized protein at a faster rate than mitochondria isolated from the heart of females (0.22+/-0. 02 versus 0.11+/-0.02 pmol phenylalanine mg(-)(1 )protein min(-)(1)). That is, 'male' mitochondria are inherently predisposed to synthesize protein at faster rates. We speculate that the difference may result from higher levels of mitochondrial RNA in males than in females. Mitochondria isolated from the heart of sexually immature rainbow trout acclimated to 13 degrees C synthesized protein at the same rate at 25 degrees C (0.456+/-0.075 pmolphenylalanine mg(-)(1 )protein min(-)(1)) and 15 degrees C (0.455+/-0.027 pmol phenylalanine mg(-)(1 )protein min(-)(1)). However, the rate of protein synthesis was severely impaired at 5 degrees C (0.125+/-0.02 pmol phenylalanine mg(-)(1 )protein min(-)(1)). Since the rate of state 3 respiration by isolated mitochondria decreased in a linear fashion over the temperature range 25 to 5 degrees C, the rate of mitochondrial protein synthesis is not directly coupled to the rate of respiration. Thermal acclimation to 5 degrees C did not result in positive thermal compensation in either the rate of protein synthesis or the rate of oxygen consumption by isolated mitochondria. In a further series of experiments, total protein synthesis and oxygen consumption were measured in isolated myocytes. The rate of oxygen consumption by myocytes remained constant over the temperature range 25 to 5 degrees C. There was no difference in the rate of total cell protein synthesis between 25 degrees C (1.73+/-0. 29 pmol phenylalanine 10(6 )cells(-)(1 )h(-)(1)) and 15 degrees C (2. 12+/-0.19 pmol phenylalanine 10(6 )cells(-)(1 )h(-)(1)), but at 5 degrees C protein synthesis was substantially impaired to approximately one-sixth of the level observed at 15 degrees C. As such, rates of total cell protein synthesis were not directly coupled to rates of respiration and were curtailed at low temperature. In vitro studies show that mitochondria isolated from the heart of sexually mature male rainbow trout are inherently different from mitochondria isolated from the heart of females such that the former are able to synthesize protein at a faster rate. The rate of mitochondrial protein synthesis does not correlate with the greater than twofold changes in rates of oxygen consumption induced by acute changes in assay temperature, suggesting that protein synthesis is not directly coupled to rates of ATP or GTP synthesis.

Journal Article↗