Biomedical subjects

R D Allrich

Publications and source records attributed to R D Allrich.

At least 19 recordsLinked to original sources

PubMed1994

Endocrine and neural control of estrus in dairy cows.

During proestrus, gonadotropins induce final follicular maturation, resulting in increased secretion of estradiol. Estradiol, in the relative absence of progesterone, acts on the hypothalamus to induce estrous behavior. The mean duration of estrus is 12 to 16 h and ranges from 3 to 28 h. The effects of estradiol appear to be "all or none". That is, once a threshold of estradiol is achieved, estrus is induced, and additional amounts of estradiol above threshold do not further enhance the estrous response (duration and intensity of estrus). Also, progesterone can block the estrus-inducing actions of estradiol. In addition, prior exposure to progesterone does not potentiate the estrus-inducing actions of estradiol except in the early postpartum period. In dairy cows, the first postpartum ovulation is often "silent". In other words, ovulation is not preceded by estrous behavior. High levels of estradiol during late gestation apparently induce a refractory state such that the brain cannot respond to the estrus-inducing actions of estradiol at the first postpartum ovulation. Progesterone can "reset" the brain, allowing it to respond to subsequent estradiol exposure. In the case of the postpartum cow, the corpus luteum formed after the first ovulation provides the progesterone that resets the brain. As a consequence, the second postpartum ovulation is preceded by estrous behavior. Finally, stress (or injection of ACTH) has been shown to delay, shorten, or inhibit completely the expression of estrus in the presence of estrus-inducing concentrations of estradiol.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1993

Estrous behavior and detection in cattle.

Hormonal events determine the timing and maximum duration of estrous behavior, whereas environmental and social factors modulate or completely inhibit the expression of estrus. The efficiency of estrous detection can be improved on most livestock farms if more effort is given to visual observations of estrous behavior. Heat detection aids can be of value if used as a supplement to visual observations. Knowledge of factors that inhibit estrus can help producers avoid or minimize situations that make estrous detection difficult or impossible. Each livestock enterprise should have a customized heat detection program in place because blanket recommendations often fail when applied to many operations.

Animals↗

PubMed1992

Influence of exogenous adrenocorticotropic hormone on estrous behavior in cattle.

A two-trial experiment was conducted to determine the influence of ACTH on estrous behavior in cattle. In Trial 1, Holstein heifers (n = 20) received an injection of prostaglandin F2 alpha (PGF) during a synchronized diestrus and 30 h later were allotted randomly to receive (i.m.) either 1) 4 mL of gelatin (Veh) or 2) 320 units of ACTH in 4 mL of gelatin (ACTH). Eleven days after the PGF injection, all heifers were again injected with PGF, and they received either Veh or ACTH to complete a cross-over design. Treatment with ACTH decreased (P less than .05) the duration of estrus (12.0 +/- 1.9 vs 18.0 +/- 1.6 h for Veh) and increased (P less than .001) the interval to estrus after PGF injection (62.9 +/- 2.6 vs 43.7 +/- 2.2 h for Veh). Peak serum concentrations of progesterone (P4) and cortisol (C) were elevated (P less than .001) after ACTH compared with Veh. In Trial 2, ovariectomized Holstein cows (n = 12) were injected (i.m.) with .5 mg of estradiol benzoate (EB) and, 10 h later, were allotted randomly to receive (i.m.) either 1) 4 mL of gelatin (Veh) or 2) 320 units of ACTH in 4 mL of gelatin (ACTH). Seven days after the initial EB injection, all cows were again injected with .5 mg of EB and, 10 h later, received either Veh or ACTH to complete a cross-over design. Treatment with ACTH decreased (P less than .01) the proportion of cows in estrus (2/12 vs 11/12 for Veh) and increased (P less than .01) peak serum concentrations of P4 and C.(ABSTRACT TRUNCATED AT 250 WORDS)

Adrenocorticotropic Hormone↗

PubMed1992

Effect of progesterone on the expression of estrus at the first postpartum ovulation in dairy cattle.

Fifty-two lactating Holstein cows were randomly assigned to receive either a progesterone-releasing (2 g of progesterone) or a control-releasing intravaginal device (0 g of progesterone). Intravaginal devices were inserted on d 10 and removed on d 15 postpartum. Daily blood samples were collected from d 10 to 90 postpartum for subsequent determination of progesterone concentrations. Observations for estrus were conducted three times daily in a dirt paddock containing a testosterone-treated cow. Serum concentrations of progesterone in the progesterone-releasing intravaginal device group were elevated on d 11, 12, 13, 14, and 15 compared with those of the control group. The days to first post-partum ovulation were similar between the treated and control groups, respectively (30.6 vs. 30.5 d). Also similar was the proportion of cows expressing estrus at first, second, and third postpartum ovulations (9/27 vs. 3/24, 14/23 vs. 15/21, and 14/21 vs. 9/15, respectively), length of the first postpartum estrous cycle (17.9 vs. 18.3 d), and peak serum concentrations of progesterone during the first estrous cycle (3.5 vs. 2.9 ng/ml). These data indicate that administration of progesterone early postpartum did not increase the proportion of cows expressing estrus at the first ovulation.

Administration, Intravaginal↗

PubMed1989

Relationship between endogenous estradiol-17 beta and estrous behavior in heifers.

Thirty-five Holstein heifers were used to examine the relationship between endogenous estradiol-17 beta and estrous traits. During a non-superovulation period (NSP), estrous cycles were synchronized and during the periovulatory stage blood samples were collected every 6 h for 120 h for subsequent determination of estradiol-17 beta and progesterone. In addition, continuous observation for estrous behavior was performed for 98 h. A gonadotropin-induced superovulation period (SP) was begun 12 d after estrus was detected during NSP. Heifers were injected with FSH twice daily for 4 d and single injections of prostaglandin were given on d 14 and 15. Beginning at d 14, blood samples were collected every 6 h for 120 h for subsequent determination of estradiol-17 beta and progesterone. Continuous observation for estrous behavior was performed for 98 h. Peak estradiol-17 beta was greater during SP than during NSP (49.0 +/- 3.1 vs 12.9 +/- 3.0 pg/ml serum). Thirty-three and 31 of the 35 heifers were in estrus during NSP and SP, respectively; duration of estrus was 2.3 h longer during SP than during NSP. However, number of behavioral interactions during estrus did not differ between NSP and SP. In conclusion, estrous traits were similar, whereas peak estradiol-17 beta concentrations were markedly different between NSP and SP.

Animals↗

PubMed1989

Influence of dexamethasone, progesterone, gonadotropin-releasing hormone, and testosterone on estrous behavior of estradiol-treated ovariectomized heifers.

In Experiment 1, 12 ovariectomized heifers were assigned to receive weekly hormone treatments in a replicated 6 x 6 Latin square design. Hormonal treatments were given as two simultaneous injections i.m. and consisted of: 1) 2 ml propylene glycol and 2 ml propylene glycol; 2) .5 mg estradiol benzoate and 2 ml propylene glycol; 3) .5 mg estradiol benzoate and 4 mg dexamethasone; 4) .5 mg estradiol benzoate and 10 mg progesterone; 5) .5 mg estradiol benzoate and .4 mg GnRH; and 6) .5 mg estradiol benzoate and 12.5 mg testosterone propionate. The .5 mg estradiol benzoate and 4 mg dexamethasone treatment reduced the percentage of heifers in estrus compared with the .5 mg estradiol benzoate and 2 ml propylene glycol treatment. In Experiment 2, 16 ovariectomized heifers were used in four replicates of a 4 x 4 Latin square design to determine if pretreatment with progesterone potentiated the actions of estradiol. Hormonal treatments i.m. consisted of: 1) 0 mg progesterone and .2 mg estradiol benzoate; 2) 50 mg progesterone and .2 mg estradiol benzoate; 3) 0 mg progesterone and .5 mg estradiol benzoate; and 4) 50 mg progesterone and .5 mg estradiol benzoate. Progesterone pretreatment, at either dosage of estradiol benzoate, did not increase the percentage of heifers in estrus. Based on these observations, we conclude that: 1) dexamethasone inhibited estrus in estradiol-treated ovariectomized heifers and 2) progesterone pretreatment did not potentiate the actions of estradiol in ovariectomized heifers.

Animals↗

PubMed1988

Influence of nutrition on serum concentrations of progesterone, luteinizing hormone and estrous behavior in dairy heifers.

Thirty postpubertal Holstein heifers were used to investigate the influence of dietary intake on 1) serum concentrations of progesterone (P4) and luteinizing hormone (LH) during diestrus and 2) estrous behavior. Heifers were randomly allotted to receive either 80, 100 or 120% of the National Research Council (NRC) requirements for energy, protein and dry matter intake for 139 d. Heifers were fed their respective diets in groups in outdoor lots for 114 d at which time individual feeding of diets was initiated in a stanchion barn. Estrus was synchronized with two injections of prostaglandin (PG) so that on d 138 of dietary treatment the heifers were in diestrus (means = d 8 of estrous cycle). Also, on d 138, blood samples were collected via jugular cannula at 20-min intervals for 12 h beginning at 0630. After collection of the 37th blood sample, all heifers were treated with PG and additional blood samples were collected at 1-h intervals for 24 h. Immediately thereafter, all heifers were moved to a common outdoor lot for 72 h of continuous observation for estrous behavior. Weight gains during the experimental period differed among groups and were 46 +/- 5, 83 +/- 5 and 113 +/- 4 kg for the heifers fed 80, 100 and 120% of the NRC requirements, respectively. Mean serum concentrations of P4 for the 80% NRC group (4.6 +/- .6 ng/ml) tended to be lower than both the 100% (5.9 +/- .6 ng/ml) and 120% (6.0 +/- .5 ng/ml) NRC groups, respectively. Mean serum concentrations of LH, number of LH secretory peaks/12 h and LH peak amplitude were similar among all NRC groups. Rate of decline in serum P4 after PG was also similar among all NRC groups.(ABSTRACT TRUNCATED AT 250 WORDS)

Animal Nutritional Physiological Phenomena↗

PubMed1987

Pituitary gonadotropins, hypothalamic gonadotropin-releasing hormone, and testicular traits of boars exposed to natural or supplemental lighting during pubertal development.

Seventy crossbred boars were reared under natural (30 lux) or supplemental lighting (1000 lux) beginning at 4 wk of age. Boars received supplemental lighting from six 40-watt fluorescent bulbs between 0530 and 2030 h. Five boars from each treatment were killed at 67, 91, 119, 155, 182, 210, or 246 days of age. No differences (p greater than 0.05) in pituitary concentrations of luteinizing hormone (LH), follicle-stimulating hormone (FSH), and prolactin (PRL) were found between treatment groups at any age. Total pituitary content of LH, FSH and PRL increased as boars became older, but when expressed as hormone concentration, only PRL increased with age. Content of gonadotropin-releasing hormone (GnRH) in the pituitary stalk-median eminence, preoptic area, and hypothalamus proper was similar (p greater than 0.05) between treatments. When GnRH contents were totaled and combined for the treatment groups, it was found that GnRH content increased (p less than 0.05) as boars became older. No differences (p greater than 0.05) were observed in testicular volume percentage of seminiferous tubules and tubular diameter between lighting treatments. These data demonstrate that the supplemental lighting does not influence puberty in boars by altering hypothalamic content of GnRH or pituitary stores of LH, FSH, and PRL.

Animals↗

PubMed1987

Hormonal patterns of boars exposed to natural or supplemental lighting during pubertal development.

Thirty-two crossbred boars (Hampshire X Duroc X Yorkshire) were reared under natural lighting (35 lx) or supplemental lighting (1,400 lx) beginning at 4 wk of age. Boars received supplemental lighting from six 40-W fluorescent bulbs between 0530 and 2030 in a nursery unit. From 9 to 32 wk of age, boars received either natural lighting (30 lx) or supplemental lighting (100 lx) in a growing-finishing unit. Blood samples were collected from indwelling cannulae at 20-min intervals for 6 h every 2 wk from 2.5 to 7 mo of age. Libido scores were evaluated during alternate weeks when intensive blood samples were not taken. Libido scores were not different between natural and supplemental lighting treatments (P greater than .30). However, at 122 d of age, libido scores of boars exposed to supplemental lighting tended to be higher (P = .10) than those exposed to natural lighting. Although mean serum concentrations of luteinizing hormone (LH) were higher (P less than .05) in boars at 75, 89, 103 and 131 d of age reared under supplemental lighting than boars of the same age reared under natural lighting, the number of LH secretory spikes was similar between the treatment groups (P = .39). Serum concentrations of LH decreased in both treatment groups as boars became older (P less than .05). However, the incidence of LH spikes was similar across ages and between treatment groups from 2.5 to 7 mo of age. Mean serum concentrations of follicle stimulating hormone and testosterone were similar between treatments (P greater than .75).

Animals↗

PubMed1987

Influence of cortisol and dexamethasone on estrous behavior of estradiol-treated ovariectomized cows and heifers.

Two experiments were conducted with estradiol-treated ovariectomized cows and heifers to determine if cortisol and dexamethasone inhibit estrous behavior. In Experiment 1, eight ovariectomized Holstein cows were subjected to weekly hormonal treatments in a replicated 4 X 4 Latin square. Treatments consisted of 500 micrograms estradiol benzoate and either 0, 40, 80, or 160 mg cortisol. During the 48 h after hormonal injection, 2-h periods of observation were alternated with 2-h periods of no observation. During each observation period, cows were observed continuously for 14 behavioral interactions that increase in frequency at estrus. Percentage of cows exhibiting estrus, interval from injection of hormones to the onset of estrus, duration of estrus, and total numbers of each behavioral interaction were similar for all treatments. In Experiment 2, 10 ovariectomized Holstein heifers were subjected to weekly hormonal treatments in a replicated 5 X 5 Latin square. Treatments consisted of 500 micrograms estradiol benzoate and either 4 mg dexamethasone, 0, 50, 100, or 200 mg cortisol. The estradiol benzoate plus dexamethasone treatment tended to lower the percentage of cattle exhibiting estrus. Interval from injection to onset of estrus, duration of estrus, and total numbers of each behavioral interaction were similar for all treatments. These data indicate that cortisol given with estradiol did not inhibit estrus in ovariectomized cows and heifers, whereas dexamethasone tended to inhibit induced estrus.

Animals↗

PubMed1986

Changes in Leydig cell ultrastructure and function during pubertal development in the boar.

Changes in the ultrastructure of Leydig cells during pubertal development in the boar (40 to 250 days of age) were assessed using quantitative morphometric procedures, and the results were compared to the in vitro steroid-producing capacity and gonadotropin sensitivity of testicular tissue obtained from the same boars. Volume of individual Leydig cells declined through 100 days of age, increased rapidly to a peak at 130-160 days (i.e., puberty), and then declined to intermediate levels by 220-250 days of age. The pattern of change in the number of intracellular organelles per Leydig cell was very similar to the change that occurred in Leydig cell volume. Changes in the total intracellular volume occupied by each type of organelle were highly correlated with changes in Leydig cell volume (r = 0.40-0.99, p less than 0.01), and this was particularly true for the nucleus (r = 0.63), mitochondria (r = 0.88), smooth endoplasmic reticulum (SER; r = 0.97), and total cytoplasm (r = 0.99) of the boar Leydig cell. In vitro production of testosterone and estradiol, expressed per Leydig cell, also peaked at 130-160 days, and was highly correlated to average Leydig cell volume, volume of SER, and number and total volume of mitochondria (r = 0.63-0.84; p less than 0.01). Observations in the present study indicated that onset of puberty in boars coincides with a dramatic increase in average Leydig cell size and SER volume per Leydig cell, accompanied by an increase in number of other intracellular organelles, including mitochondria, lysosomes, and lipid droplets, and a peak in the steroid-producing capacity per Leydig cell. A decline in Leydig cell size, intracellular organelles, and sensitivity to gonadotropin stimulation occurred postpubertally.

Aging↗

PubMed1986

Anterior pituitary concentrations of gonadotropins, GnRH-receptors and ovarian characteristics following early weaning in beef cows.

Endocrine changes in the hypophyseal-ovarian axis associated with early calf removal were investigated in anestrous beef cows. Tissues were collected and analyzed from multiparous beef cows slaughtered at O (n = 8), 36 (n = 8) or 72 h (n = 8) after calf removal during the fifth week after calving. Cows that exhibited estrus; had postmortem signs of a recent ovulation or had serum concentrations of luteinizing hormone (LH) indicative of an ovulatory surge, were excluded from the analysis. Five control cows that were not slaughtered exhibited estrus from 30 to 84 h after calf removal. Seven additional cows were continuously kept with their calves and did not exhibit estrus until 72 +/- 9 d after calving. Serum concentrations of estradiol-17 beta (estradiol) averaged 8.2 +/- 1.7, 7.5 +/- 2.0 and 9.1 +/- 1.5 pg/ml at 0, 36 and 72 h, respectively, but they averaged 22.8 +/- 4.7 pg/ml prior to estrus in control cows. Therefore, observations were assumed to represent events that occur prior to the rise in serum concentrations of estradiol that occurs during proestrus. Volume of fluid from the largest ovarian follicle tended to be greater (P less than .10) at 72 h (1.5 +/- .2 ml) than at 0 h (1.1 +/- .1 ml) or 36 h (1.0 +/- .1 ml). Follicular-fluid concentrations of estradiol, but not progesterone, were positively correlated (P less than .01) with follicular volume. However, numbers of small (less than 100 microliters), medium (100 to 400 microliters) and large follicles (greater than 400 microliters) as based on fluid volume, as well as follicular-fluid concentrations of estradiol and progesterone, did not differ among treatment groups.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1986

Relationships among concentrations of four opioid neuropeptides and luteinizing hormone-releasing hormone in neural tissues of beef cows following early weaning.

Acute changes associated with removal of the inhibition of estrus caused by suckling were examined in beef cows. Calves were weaned during the fifth week after parturition and cows were slaughtered at 0 (n = 8), 36 (n = 8) or 72 h (n = 8) after calf removal. Tissues of preoptic area (POA), hypothalamus (HYP), pituitary stalk-median eminence (SME) and pituitary neurointermediate lobe (NIL) were obtained for analyses of luteinizing hormone-releasing hormone (LHRH) and four opioid neuropeptides. In addition, one-half of each SME was superfused in vitro for measurement of basal and potassium-induced release of LHRH. The following opioid neuropeptides were quantified: methionine-enkephalin (Met-Enk), beta-endorphin (beta-EP), dynorphin-A, 1-17 (DYN-17) and dynorphin-A, 1-8 (DYN-8). All four opioid neuropeptides were most concentrated in the pituitary NIL. Luteinizing hormone-releasing hormone was most concentrated in the SME tissue, which also contained substantial concentrations of Met-Enk and beta-EP, but very little DYN-17 or DYN-8. In addition, weaning increased the weight of NIL between 0 and 36 h (P less than .05), and the concentrations of LHRH, Met-Enk, and DYN-17 in the combined POA + HYP (P less than .05) tissue between 36 and 72 h. No differences occurred among groups in SME content of LHRH or in vitro release of LHRH from the superfused SME. Although they were not affected by weaning, within-cow correlations among parameters revealed that: 1) concentrations of DYN-17 and DYN-8 were always positively correlated (P less than .05); 2) concentrations of LHRH were positively correlated with Met-Enk (P less than .01), beta-EP (P less than .05) and DYN-17 (P less than .05) in the combined POA + HYP tissue; 3) LHRH concentrations in SME tissue were negatively related to POA + HYP concentrations of Met-Enk (P less than .01) and beta-EP (P less than .05), but not of LHRH or DYN-17 and 4) in vitro release of LHRH from the pituitary SME was correlated with concentrations of DYN-8 in various tissues including the SME (P less than .01). In summary, bovine neural tissues differ widely in concentrations of the four opioid neuropeptides with NIL tissue having the greatest concentrations. Weaning calves at 36 and 72 h before slaughter caused parallel changes in LHRH, Met-Enk and DYN-17 in preoptic and hypothalamic tissues.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

PubMed1986

Induction of estrus in ovariectomized cows and heifers: effects of estradiol benzoate and gonadotropin releasing hormone.

Three experiments were conducted with ovariectomized (OVX) cows and heifers to investigate potential neuroendocrine mechanisms controlling estrous behavior. In Exp. 1, 10 OVX cows were treated with either 125 micrograms estradiol benzoate and 10 cc saline (125 micrograms EB + SAL), 125 micrograms EB and 500 micrograms gonadotropin releasing hormone (125 micrograms EB + GnRH), 250 micrograms EB and 10 cc SAL (250 micrograms EB + SAL), 250 micrograms EB and 500 micrograms GnRH (250 micrograms EB + GnRH) or 500 micrograms EB and 10 cc SAL (500 micrograms EB + SAL) in a replicated 5 X 5 Latin-square design. During the 48 h following EB injection, 2-h observation blocks were alternated with 2-h non-observation blocks. During each 2-h observation block, 14 behavioral interactions were monitored. The percentage of cows in estrus was lower for cows receiving 125 micrograms EB as compared with those given the higher doses. However, the cows receiving 125 micrograms EB + SAL did not differ in their estrous response from those receiving 125 micrograms EB + GnRH. The interval from injection to the onset of estrus and the duration of estrus were similar for all treatments. In Exp. 2, 10 OVX heifers were subjected to the same treatments and observation procedures utilized in Exp. 1. The results of Exp. 2 were similar to those of Exp. 1. In Exp. 3, 10 OVX cows were treated with either 300, 600, 1,200, 2,400 or 4,800 micrograms EB in a replicated 5 X 5 Latin-square design.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1985

Pituitary concentrations of gonadotropins and receptors for GnRH in suckled beef cows at various intervals after calving.

Mature beef cows were slaughtered at 5 (n = 6), 10 (n = 6), 20 (n = 6) or 30 (n = 5) d after calving to identify endocrine events that may affect the duration of postpartum anestrus. Additional cows (n = 6) were slaughtered 12 to 14 d after their first postpartum estrus (luteal phase cows). Anterior pituitary concentrations of luteinizing hormone (LH) were low at d 5 (383 +/- 69 micrograms/g), averaged 445 +/- 103 and 682 +/- 207 micrograms/g at d 10 and 20, respectively, and were elevated (P less than .05) by d 30 (1,097 +/- 174 micrograms) to a concentration similar to luteal phase cows (1,208 +/- 148 micrograms/g). Concentrations of follicle-stimulating hormone (FSH) averaged 12.4 +/- 1.1, 9.6 +/- 2, 8.6 +/- 1.8 and 7.4 +/- 3.3 mg/g at d 5, 10, 20 and 30, respectively. Affinity (1.6 +/- .2 X 10(9) M-1) of anterior pituitary receptors for the GnRH (gonadotropin-releasing hormone) analog (DAla6; des-Gly10, [D-Ala6]-LH-RH ethylamide) and weights (2.1 +/- .1 g) of the anterior pituitaries did not differ among groups (P greater than .05). Number of receptors for GnRH averaged 37 +/- 7, 39 +/- 9, 25 +/- 5 and 23 +/- 5 X 10(-14) M/mg protein at d 5, 10, 20 and 30, respectively. Anterior pituitaries from luteal phase cows contained 22 +/- 2 X 10(-14) M/mg protein of receptors for GnRH.(ABSTRACT TRUNCATED AT 250 WORDS)

Anestrus↗

PubMed1984

Characterization of luteinizing hormone-human chorionic gonadotropin receptor and its relationships to testicular development and steroidogenesis during sexual maturation in boars.

Luteinizing hormone-human chorionic gonadotropin (LH-hCG) binding capacity for testes of boars and receptor sites per Leydig cell were estimated during pubertal development from 70 to 250 days of age, and changes in these two traits were correlated with morphological and endocrine parameters. Binding capacity increased linearly from 70 to 160 days of age, remained constant through 250 days of age, and was correlated (P less than 0.05) with paired testes weight, Leydig cell number and weight per paired testes, and serum estradiol-17 beta (E2) concentrations. LH-hCG receptor sites per Leydig cell were constant at all ages except for an increase observed at 160 days of age and were correlated (P less than 0.05) to in vitro maximum testosterone (T) production and sensitivity of E2 production per Leydig cell in response to hCG stimulation. Number of LH-hCG receptor sites was correlated (P less than 0.05) with Leydig cell surface area, and sites per unit surface area increased with age. Equilibrium association constants did not differ with age, and they averaged 8.6 +/- 1.0 X 10(9) M-1. Results from the present study indicate that LH-hCG receptor capacity per paired porcine testes increases throughout pubertal development primarily as Leydig cell numbers increase.

Animals↗

PubMed1983

Pubertal development of the boar: age-related changes in testicular morphology and in vitro production of testosterone and estradiol-17 beta.

The responsiveness of testicular tissue, in terms of testosterone (T) and estradiol-17 beta (E2) production, to human chorionic gonadotropin (hCG) stimulation in vitro was assessed during pubertal development of the boar. A morphometric investigation was conducted concurrently to quantitate Leydig cell and seminiferous tubule changes in the testes of developing boars. Testicular volume percentage of seminiferous tubules increased from 36% at 40 days of age to a maximum of 72% at 190 days of age. Increases in tubular diameter were from 65 micrometers at 40 days of age to 236 micrometers at 250 days of age. Testicular volume percentage of Leydig cells decreased from 40% at 40 days of age to 10% at 250 days of age. Leydig cell number increased rapidly to 130 days of age, remained constant through 160 days, and then increased steadily to 220 days of age. Volume per Leydig cell changed little from 40 to 130 days of age, increased by 75% at 160 days, and declined thereafter. Total Leydig cell weight increased steadily from 40 to 160 days of age and then declined slightly. The capacity of Leydig cells for T production and testicular tissue for E2 production was greatest (P less than 0.05) after hCG stimulation in boars that were 130 and 160 days of age. In addition, sensitivity, as judged by the regression coefficient of T or E2 production per Leydig cell on log dosage of hCG was greater (p less than 0.05) for T at 130 days of age and for E2 at 160 days of age. The data presented support the hypothesis that one factor in pubertal development of boars is an increased capacity and sensitivity of the testes to gonadotropin stimulation.

Aging↗

PubMed1982

Pubertal development of the boar: testosterone, estradiol-17 beta, cortisol and LH concentrations before and after castration at various ages.

Forty-eight Landrace x Duroc boars were assigned at weaning to eight castration ages (40, 70, 100, 130, 160, 190, 220 and 250 d). Catheterization of the external jugular vein was performed 5 d before scheduled castration. Blood samples were collected every .5 h between 0800 and 1200 h, 2 d before (-2) and on d +1, +2, +3, +4, +8 and +16 after castration. Testosterone (T) was determined in serum samples collected every .5 h on d -2. Serum concentrations of estradiol-17 beta (E2), cortisol (C) and luteinizing hormone (LH) were quantified by radioimmunoassays in pooled (within boar) samples collected on d -2. In addition, LH was determined in pooled (within boar) samples collected on d +1, +2, +3, +4, +8 and +16 after castration. Mean concentrations of T and E2 (d -2) increased in a near linear (P less than .01) fashion with age of boar. However, T concentrations at 250 d of age had declined (P less than .01) to values similar to concentrations of boars at 130 d of age. Serum C concentrations (d -2) were lower (P less than .01) at 100, 130 and 160 d of age compared with an average C concentration of 19 ng/ml for all other age groups. Mean concentrations of LH (d -2) did not differ among any of the ages. Luteinizing hormone concentrations were elevated (P less than .01) within 1 to 2 d following castration at 40, 70, 100, 130 and 160 d of age. Serum T concentrations of individual boars varied greatly at all ages as determined by half-hourly sampling over a 4-h period. The results indicate that in the boar: (1) T concentrations increase as pubertal development progresses and decline as maturity nears; (2) E2 concentrations increase steadily through pubertal development; (3) C concentrations are depressed at 100, 130 and 160 d of age relative to concentrations before and after that period; (4) LH concentrations are constant during pubertal development, and (5) a decrease in the sensitivity of the negative feedback mechanism controlling LH occurs after 160 d of age.

Aging↗