PubMed Health⌕ Search

Biomedical subjects

M Terqui

Publications and source records attributed to M Terqui.

At least 55 records · Page 3Linked to original sources

Variations in testicular androgen receptors and histology of the lamb testis from birth to puberty.

Changes in testicular androgen receptor numbers were studied in lambs from 25 to 100 days of age. During this period, cytoplasmic receptors increased from 5 to 80 pmol/testis and nuclear receptors from 1 to 12 pmol/testis, while the total volume of Leydig cells increased 7-fold. The total number of Sertoli cells doubled between 25 and 40 days of age. From 40 days onward their number remained constant while their cellular and nuclear sizes increased by a factor of 3 and 1.5 respectively. Cytoplasmic receptor concentration was positively correlated with the number of Sertoli cells per section of seminiferous tubule, and negatively correlated with the number of germinal cells per cross section. One explanation for these results could be that Sertoli cells are the main androgen target cells in lamb seminiferous tubules.

Animals↗

Effect of confinement, climatic conditions and litter parity on the seasonal variations of the fertility rate and prolificacy.

Prolificacy and fertility in sows were analysed according to the month of service, the regional locations of the herd, the type of building (confinement or open front) and the parity of the sows. Fertility varied throughout the year and was lowest in August, September and October. The regional location of the herd had little or no effect. Primiparous sows were less fertile than multiparous sows, regardless of the type of building. Results for closed buildings were better than those for semi-outdoor quarters. This difference was maximum (8%) for matings in August, September and October. Prolificacy also varied with season but was relatively unaffected by the type of housing. The largest litters were conceived in summer when the ovulation rate was highest. The extend of seasonal variation in prolificacy was higher in Brittany than in the South of France in which hot climatic conditions are more frequent in summer. The month of service and the type of housing appear to be the most important factors conditioning the annual productivity of sows.

Animals↗

Nuclear testosterone receptors in the ovine testis.

Nuclear [3H] testosterone-receptor complexes were demonstrated in hypophysectomized ram testis after in vitro direct labelling. The nuclear binding was maximal after a 45 min incubation of the tissue. The receptors are extractable by 0.4 M KC1 or NaSCN with a 25-30% efficiency. They migrate towards the anodic region during electrophoresis on agar gel. Nuclear androgen receptors were characterized in intact lamb testis by a testosterone exchange assay. After precipitation by protamine sulphate, the receptors were labelled with [3H]testosterone during a 12 h incubation at 4 degrees C. The exchange activity was linear between 0.1 and 0.9 mg of DNA per ml of incubation buffer. The receptors bind testosterone with a limited capacity (40-180 fmoles per mg DNA) and a dissociation constant Kd of 2 x 10(-9) M. Their relative affinities for steroids are dihydrotestosterone greater than testosterone greater than estradiol greater than progesterone greater than 5 alpha-androstanediol greater than cyproterone acute greater than R5020.

Animals↗

A note on the metabolism of 5 alpha-androst-16-en-3-one in the young boar in vivo.

The metabolism of plasma 5 alpha-androst-16-en-3-one (androstenone) was studied in two young boars weighing about 100 kg in which a single dose of tritiated androstenone was injected intravenously. The peripheral blood of one boar was continuously sampled for 6 h after injection; the total radioactivity per liter of plasma increased up to 14 min after the injection, and then declined rather slowly since plasma radioactivity was still measurable 7 days after injection. The metabolic clearance rate of androstenone was calculated to be about 80 000 liters per day. This quick disappearance of plasma androstenone was probably mainly due to storage in fatty tissue and, to a lesser extent, to catabolism into 5 alpha-androst-16-en-3 alpha-ol, 5 alpha-androst-16-en-3 beta-ol and particularly into unknown more polar compounds of which there were at least three. Radioactivity was mainly eliminated in the urine in the form of the same unknown polar compounds.

Androstenes↗

Hormone levels in plasma of ewes induced into lactation.

A short-term treatment with estradiol-17 beta and progesterone induced mammary gland growth and lactogenesis in non-pregnant ewes. These events normally occur during the second half of pregnancy. In order to compare the hormonal environment during the treatment to that during pregnancy, the concentrations of total estrogens (TE), progesterone (P4), glucocorticoids (G) and prolactin (Prl) in the plasma were characterized in non-pregnant, intact ewes induced into lactation with subcutaneous injections of estradiol-17 beta (E2-beta) and P4 for 7 consecutive days (days 1 to 7). Eight non-pregnant, intact, multiparous ewes were divided into two groups (groups I and II, 4 ewes each), according to their milk yields recorded during the previous lactation. All the ewes received the short-term treatment with E2-beta and P4; the ewes of group II were also injected with hydrocortisone acetate (H) and growth hormone (GH) twice daily on days 18 to 20. Blood was collected twice daily for 21 days and milking was initiated 19 days after the first injection of E2-beta and P4. Concentrations of TE, P4, G and Prl were measured in the plasma of ewes in group I but only G and Prl were measured in the plasma of the ewes in group II. Two ewes of group I and one of group II failed to lactate. Mean milk yields (2.5 +/- 0.4 and 6.3 +/- 0.9 kg/34 days) were highest when injections of H and GH were included. Average pretreatment concentrations of plasma TE and P4 were 3.1 +/- 0.8 and 2.1 +/- 0.4 ng/ml, respectively; these increased to 10.2 +/- 1.3 and 5.6 +/- 0.6 ng/ml during the week of the E2-beta and P4 injections. Peak concentrations occurred on days 7 and 6, respectively, and the plasma levels had returned to pretreatment values by days 18 to 20. Concentrations of G in plasma were higher (13.0 +/- 1.0 ng/ml) during E2-beta and P4 injections than during pre- or post-injection (7.4 +/- 1.4 and 8.2 +/- 0.7 ng/ml, respectively). Plasma Prl showed biphasic two to six-fold increases on days 4 and 7 during E2-beta and P4 injections and thereafter declined to lower average daily concentrations on days 10 to 13. Plasma Prl began to increase, and its average concentration was 579 +/- 56 ng/ml by days 18 to 20. These results suggest that the amount of the P4 injections should be increased and that the treatment with E2-beta and P4 should last long enough to insure the induction of an endocrine balance which would correspond more accurately to the hormonal events occurring during the second half of pregnancy in the ewe.

Animals↗

Influence of 2 Br-alpha-ergocryptine (CB 154) on the secretion of prolactin, LH, FSH and testosterone and on testicular growth in rams subjected to different photoperiods.

The influence of 2-Br-alpha-ergocryptine (CB 154) on the secretion of gonadotrophins and on testicular function has been studied in rams subjected to either a normal photoperiod or an abnormal photoperiod causing hyperprolactinaemia. The CB 154 treatment significantly lowered the mean frequency of LH and testosterone pulses in hyperprolactinaemic animals as compared to solvent-treated ones. Also, only those groups subjected to an abnormal photoperiod (groups 2 and 3) exhibited a significant rise in the frequency of LH and testosterone peaks after CB 154 was withdrawn. During treatment, plasma FSH concentrations increased significantly only in group 1 which was subjected to normal photoperiodic variations. Testicular growth was delayed in CB 154-treated rams compared to solvent-treated ones only in group 3 (hyperprolactinaemic).

Animals↗

Seasonal variation in LH and testosterone release in rams of two breeds.

Blood was collected hourly for 24 h in December, February, April, June and September from Préalpes du sud and Ile-de-France rams. Coincidence of the LH and testosterone peaks was found for 96.4% of a total of 670 LH peaks and 647 testosterone peaks. The number of LH and testosterone peaks increased by 66% in Ile-de-France rams and 200% in Préalpes du Sud rams between December and June (P less than 0.001). Values in June and September were similar in Préalpes du Sud rams. There were no differences between breeds in December, but in June, Préalpes du Sud had significantly more peaks than did Ile-de-France rams (P less than 0.025). The numbers of LH and testosterone peaks increased significantly (P less than 0.05) in Préalpes du Sud rams between December and February or April. These results indicate that, although numbers of peaks of LH and testosterone increase when the animals pass from the non-breeding to the breeding season, the genotype influences the pattern of release through the year.

Animals↗

Diurnal variation in release of LH and testosterone in the ram.

The time of appearance of plasma LH and testosterone peaks through the day determined in 75 Préalpes du Sud and 41 Ile-de-France rams in December and in 44 Préalpes du Sud and 11 Ile-de-France rams in June. The distribution of peaks throughout the day was non-random for the two hormones in the two breeds and for both times of the year (P less than 0.01 at least on each occasion; P less than 0.001 on pooled data from the two breeds). The most striking features were the occurrence of (1) a minimum of LH and testosterone peaks immediately after 'dawn' (lights on) in both months; (2) a maximum of peaks 3 h after 'dawn' in June and 4 h after 'dawn' in December. For several hours after the increase in frequency of peaks the probability of measuring peaks of LH values in December and June when adjusted for the time of 'dawn' suggest that dawn could act as a synchronizer of gonadotroph activity.

Animals↗

[Mathematical model on the development of progesterone in the cow: application and proof of differences between breeds].

Peripheral plasma progesterone levels were compared in "Normandy" (6), "Charolais" (6) and French Friesian (6) heifers. The progesterone curves were fitted to mathematical models for the luteal phase (a logistic function) and for the luteolytic phase (an exponential model). 1. Discriminating and multivariate analyses showed a breed difference in luteal phase duration (17.8 +/- 1.1, 16.8 +/- 2.3, 16.1 +/- 1.06 days, respectively, for Normandy, Charolais and French Friesian heifers) and in the rate of progesterone level increase (1.1 +/- 0.4, 1.09 +/- 0.3, 1.3 +/- 0.3 ng/ml/day, respectively) (chi 2 = 22.5; P less than 0.02). 2. Progressive multiple regression showed the duration of the luteal phase was highly correlated to oestrous cycle duration (20.8 +/- 1.7, 20.5 +/- 2.8, 19.2 +/- 1.5 days, respectively) (r = 0.89). It appears that breed differences in bovine oestrous cycle duration are due to differences in luteal phase duration. 3. The rate of progesterone level increase reached a maximum at 7.2 +/- 0.8, 6.9 +/- 1.1 and 6.4 +/- 0.6 days, respectively, concomitant with maximal corpus luteum secretion. 4. The reproducibility of these parameters, summarizing the progesterone pattern during two consecutive oestrous cycles, showed that each animal had an individual secretion pattern.

Animals↗

Effects of various hormone treatments on induction of lactation in the ewe.

In Exp. I and II, 52 of 68 ewes were induced into lactation with twice-daily injections of estradiol-17 beta (E2-beta) and progesterone (P4; .5 and 1.25 mg/kg body weight/day) for 7 days. Additional treatments were twice-daily injections (days 18 to 20) of hydrocortisone, growth hormone, thyroxine and thyrotropin releasing hormone alone or in various combinations. In Exp. III, 12 ewes were induced into lactation. In this experiment, all ewes were injected with E2-beta and hydrocortisone, as previously, but four ewes (III-2) had P4 injections extended to day 20, and four ewes (III-3) were not injected with P4. Across experiments, lowest milk yields during lactation and the lowest percentage of ewes induced into lactation (58%) occurred when only E2-beta and P4 were injected. Inclusion of hydrocortisone injections (50 mg/day) induced the highest percentage of ewes into lactation (86%, 38 of 44), the highest peak daily yields of milk and the highest total yields during lactation. Including injections of growth hormone, thyroxine or thyrotropin releasing hormone alone or in combinations did not produce better results than injections of E2-beta and P4 alone. Injections of E2-beta and hydrocortisone without concurrent injections of P4 were less effective. Intramuscular injections of P4 (10 mg/day) from days 8 to 20 did not inhibit lactogenesis or subsequent lactation. Across all experiments, 76% of multiparous (52/68) and 50% of nulliparous (6/12) ewes produced greater than 100 ml milk/day during their lactation (34 to 95 days). However, yields of milk for ewes that lactated were only 25 to 50% of those from postpartum ewes. The importance of including injections of hydrocortisone in the induction procedure was established, but determination of optimum time to inject and potential importance of other hormones requires additional research.

Animals↗

[Plasma testosterone level and structure of the epididymis and accessory organs of the boar (Sus scrofa L.) after hypophysectomy followed by hCG gonadotropin administration].

Hypophysectomy of the boar resulted in a rapid drop in plasma testosterone level. hCG injections (400 IU/day) considerably elevated testosteronemia (up to 16.41 ng/ml). This effect was obtained either in the days following the operation or several months after (up to 134 days). In the latter case, the effect was temporary because the testosterone level dropped again after 15 days of injections. The sexual target organs (epididymis, seminal vesicle, prostate and Cowper glands) underwent structural change which, in the epithelium, corresponded to fluctuations in testosterone level. These effects were less marked in the cauda epididymis than in other target tissues. In various target organs, the conjunctivomuscular stroma developed after the operation; it did not regress at all, or incompletely, when the epithelia were stimulated indirectly by hCG, and began to hypertrophy when the hCG was no longer effective. Variations in stromal reaction were organ-dependent. When the hCG was administered for more than 14 days, it seemed to have a desensitizing effect; these mechanisms have been discussed.

Animals↗

Characterization of a cytoplasmic androgen receptor in the ram testis.

An androgen receptor has been characterized in the cytosol fraction of testes from hypophysectomized adult rams after in vitro labelling with [3H]testosterone. It can be distinguished from the testicular androgen-binding protein (ABP) and from the plasma 5 alpha-dihydrotestosterone-binding protein by electrophoresis on 3.25% acrylamide gels (Rx = 0.5) and on agar gels (anodic migration). It sediments in the 4S region in sucrose gradient containing 0.4 M KCl. Its complex with testosterone dissociates very slowly (t 1/2 = 29 h at 0 degrees C), and is destroyed by heating at 50 degrees C for 30 min and by pronase. Its relative affinities for steroids are 5 alpha-DHT greater than T greater than 5 alpha-androstanediols greater than cyproterone acetate greater than estradiol greater than progesterone. The number of binding sites is limited (about 20 fmoles/mg protein) and the apparent equilibrium dissociation constant (KD) is 5 x 10(-9) M.

Adsorption↗

Periovulatory gonadotrophin and ovarian steroid patterns in sheep of breeds with differing fecundity.

Plasma hormone concentrations before and during luteolysis (induced by injection of a prostaglandin analogue on Day 10 or 11 of the cycle), during the period of preovulatory follicle growth and ovulation were examined in sheep with known differences in ovulation rate (Romanov, Préalpes, Romanov x Préalpes cross, Ile de France). The number of CL at the time of treatment and the ovulation rate in the ensuing cycle were established by endoscopy. Plasma concentrations of FSH, LH, progesterone and total oestrogen were measured by radioimmunoassays in the 3 days before PG injection, then hourly for the 24 h after PG injection and 2-hourly for a further period up to about 100 h after PG injection. The onset and duration of oestrus were also recorded. Although breed differences were observed for many of the features studied, only the intervals between oestrus and the LH peak and between PG injection and the LH peak were significantly correlated with ovulation rate.

Animals↗

Biochemical and physiological studies of androgen-binding protein in the reproductive tract of the ram.

The electrophoretic mobility, effect of pronase, temperature stability, affinity constant and specificity of androgen-binding protein (ABP) were compared in rete testis fluid (RTF), cauda epididymal plasma (CEP) and seminal plasma (SP) of the ram in which the levels of ABP, dihydrotestosterone (DHT), total protein and the number of spermatozoa were also measured. The characteristics of the ABP appeared to be almost identical in all 3 fluids. ABP was highly concentrated in the cauda epididymidis although 50-75% of it was utilized or destroyed during transit through the epididymis. The levels of ABP were higher in the breeding season and positively correlated with DHT in RTF and SP. It is concluded that ABP might be responsible for the increase in DHT in the reproductive tract of the ram during the breeding season and that ABP in the SP might serve as a useful marker of Sertoli cell function in the ram.

Androgen-Binding Protein↗

Oestrogen pattern during early pregnancy in the mare.

Plasma total (conjugated + unconjugated) oestrogens were measured from Day 0 to 100 of pregnancy and compared with the levels found during the oestrous cycle. From Day 0 to 35 of gestation, the concentrations were similar to those during dioestrus. An increase in total oestrogens between Days 35 and 40 was followed by a plateau of 3 ng/ml between Days 40 and 60 which was slightly higher than preovulatory concentrations. This first increase in total oestrogen level was produced by the ovaries since values were suppressed after ovariectomy; stimulation may be due indirectly to PMSG causing follicular growth. After Day 60, a second increase was detected and considered to be of feto-placental origin as the levels at this time were not suppressed after ovariectomy. By Day 85, oestrogen concentrations exceeded thos detected in non-pregnant mares so that a direct measurement of total oestrogens in plasma by a simplified radioimmunoassay after Day 85 of gestation offers a reliable method of pregnancy diagnosis.

Animals↗