Effect of neonatal or adult heat acclimation on plasma fT3 level, testicular thyroid receptors expression in male rats and testicular steroidogenesis in vitro in response to triiodothyronine treatment.

This study aimed to evaluate the effect of heat acclimation of neonatal and adult rats on their testes response to in vitro treatment with triiodothyronine (T3). Four groups of rats were housed from birth as: 1) control (CR) at 20°C for 90 days, 2) neonatal heat-acclimated (NHA) at 34°C for 90 days, 3) adult heat-acclimated (AHA) at 20°C for 45 days followed by 45 days at 34°C and 4) de-acclimated (DA) at 34°C for 45 days followed by 45 days at 20°C. Blood plasma and both testes were harvested from 90-day old rats. Testicular slices were then submitted to in vitro treatment with T3 (100 ng/ml) for 8 h. Plasma fT3 level was lower in AHA, NHA and DA groups than in CR group. Basal thyroid hormone receptor α1 (Thra1) expression was higher in testes of NHA and DA and ß1 receptor (Thrb1) in DA rats vs. other groups. In the in vitro experiment, T3: 1) decreased Thra1 expression in all groups and Thrb1 in DA group, 2) increased Star expression in CR, NHA and DA groups, and Hsd17b3 expression in NHA group, 3) decreased the expression of Cyp11a1 in NHA and DA groups, and Cyp19a1 in all the groups, 4) did not affect the activity of steroidogenic enzymes and steroid secretion (A4, T, E2) in all the groups. These results indicate, that heat acclimation of rats, depending on their age, mainly affects the testicular expression of steroidogenic enzymes in response to short-lasting treatment with T3.

Effect of neonatal or adult heat acclimation on testicular and epididymal morphometry and sperm production in rats.

The accessory gland weight, testicular and epididymal morphometry and sperm production were analyzed in four groups of rats housed at 20 or 34°C: (1) control rats (CR) kept at 20°C from birth to day 90; (2) adult heat-acclimated rats (AHA) kept at 20°C from birth to day 45 followed by 34°C to day 90; (3) neonatal heat-acclimated rats (NHA) kept at 34°C from birth to day 90 and (4) de-acclimated rats (DA) kept at 34°C from birth to day 45 followed by 20°C to day 90. In NHA and DA rats, accessory gland weight was higher than in controls. Despite the lack of differences in testicular and epididymal morphometry, curvilinear velocity of spermatozoa was lower in the NHA group compared to controls. Areas of seminiferous tubules were lower in the DA than in CR and NHA groups, however, sperm concentration and motility were not affected by the treatment in this group. In AHA rats, epithelium of approximately 20% of seminiferous tubules was degenerated and Sertoli cell number was lower in the remaining tubules. In contrast to sperm motility, epididymal duct area, area of the duct occupied by spermatozoa and cauda epididymis sperm concentration were lower in AHA rats than in the other groups. In conclusion, neonatal heat acclimation did not affect the testicular morphometry and epididymal sperm concentration, suggesting adjustment to high ambient temperature. On the contrary, adult heat acclimation of rats affected the examined parameters, leading to decreased sperm concentration.

The effect of tumor necrosis factor α (TNFα), interleukin 1ß (IL1ß) and interleukin 6 (IL6) on endometrial PGF2α synthesis, metabolism and release in early-pregnant pigs.

Cytokines produced by the porcine uterus and embryos may be involved in the regulation of endometrial prostaglandin synthesis, metabolism, and release. We studied the effect of tumor necrosis factor α (TNFα), interleukin 1ß (IL1ß) and interleukin 6 (IL6) on: 1) endometrial release of prostaglandin F2α (PGF2α), 2) expression of the terminal enzyme of PGF2α synthesis--PGF synthase mRNA (PGFS mRNA), 3) secretion of PGF(2)α metabolite--13,14-dihydro-15-keto PGF2α (PGFM) by the endometrium and 4) presence and activity of endometrial NAD-dependent 15-hydroxyprostaglandin dehydrogenase (15-PGDH). The effects of cytokines were determined on days 10-11 and days 12-13, e.g., before and during maternal recognition of pregnancy, and on days 15-16, e.g., during the peri-implantation period and compared with its effect in cyclic gilts on corresponding days of the estrous cycle. TNFα did not affect endometrial release of PGF2α in pregnant and cyclic pigs. IL1ß enhanced endometrial PGF2α release on days 12-13 and 15-16 in pregnant and cyclic pigs, respectively. IL6 increased PGF2α release mainly on days 15-16 of pregnancy. Expression of PGFS mRNA was decreased by IL1ß on days 12-13 of pregnancy (P<0.05) and increased in response to IL1ß, TNFα and IL6 on 12-13 (P<0.05) and 15-16 (P<0.01) of the estrous cycle. IL1ß increased release of PGFM in gravid pigs on days 12-13, 15-16 and in non-gravid pigs 10-11 and 15-16 of the cycle. On days 15-16 of pregnancy TNFα and IL6 increased endometrial secretion of PGFM. We determined that in porcine endometrium NAD-dependent 15-hydroxyprostaglandin dehydrogenase (15-PGDH) is present. In gravid pigs, the highest expression of endometrial 15-PGDH occurred during days 12-13 of pregnancy, while in non-gravid pigs during days 10-11 of the estrous cycle. These data provide new evidence that TNFα, IL1ß, IL6 are involved in the regulation of endometrial synthesis, release and metabolism of PGF2α to protect CL during early pregnancy or to facilitate its regression in cyclic females.

The effect of progesterone on oxytocin-stimulated intracellular Ca2+ mobilisation and prostaglandin secretion in porcine endometrium.

We have studied in the porcine endometrium the expression of oxytocin receptor (OTR) mRNA and the effect of progesterone (P4) on oxytocin/oxytocin receptor (OT/OTR) function concerning intracellular Ca2+ mobilisation ([Ca2+]i), prostaglandin F2alpha (PGF2alpha) and E2 (PGE2; PG) secretion. Tissue was taken from cyclic and early pregnant pigs (days 14-16). A higher expression of OTR mRNA (P < 0.05) was observed in the endometrium of cyclic than pregnant pigs. The stimulatory (P < 0.05) effect of OT (10(-7) M) on [Ca2+]i mobilisation was noticed within 15-60 s and 30-60 s in endometrial stromal cells of cyclic and pregnant pigs, respectively. In the presence of P4 (10(-5) M) basal and OT-stimulated [Ca2+]i concentrations decreased in stromal cells during luteolysis and pregnancy. In stromal cells P4 delayed mobilisation of [Ca2+]i in response to OT by 15 s during luteolysis and had no effect during pregnancy. In cyclic and pregnant epithelial cells OT stimulated mobilisation of [Ca2+]i in 45 s and 60 s, respectively. Oxytocin increased (P < 0.05) PGF2alpha secretion during luteolysis and pregnancy and PGE2 during luteolysis from endometrial slices. Progesterone did not inhibit this stimulatory effect. During luteolysis OT increased (P < 0.05) PGF2alpha in epithelial and stromal cells and PGE2 secretion in epithelial cells. In the presence of P4 this effect of OT was reduced only in stromal cyclic cells (6 h culture). The presence of P4 decreased the effect of OT on [Ca2+]i mobilisation only in stromal cells. We found that, in most conditions, P4 did not inhibit the OT-stimulated secretion of PG in the porcine endometrium.

Interleukin 1ß-induced synthesis and secretion of prostaglandin E2 in the porcine uterus during various periods of pregnancy and the estrous cycle.

Peri-implantation porcine embryos express interleukin-1ß (IL-1ß), which could affect uterine activity during early pregnancy. In vitro studies were conducted to determine if IL-1ß stimulates secretion of PGE2 and expression of cyclooxygenase-2 (COX-2) mRNA and microsomal PGE synthase-1 (mPGES-1) mRNA in uterine tissues harvested from pigs on days 10 to 11, 12 to 13 and 15 to 16 of pregnancy and the estrous cycle. IL-1ß (10 ng/ml) increased PGE2 secretion and mPGES-1 mRNA expression in uterine tissues isolated from pigs between days 10 to 13 of pregnancy and the estrous cycle. IL-1ß stimulated PGE2 and mPGES-1 mRNA expression only in cyclic uterine tissues on days 15 to 16. Interleukin-1ß increased COX-2 mRNA expression in the endometrial tissues of pregnant and cyclic pigs harvested on days 10 to 13. It stimulated COX-2 expression in pregnant pigs' myometrial tissues on days 10 to 11, and on days 15 to 16 in tissues from both pregnant and cyclic pigs. The uterine secretion of PGE2 in response to IL-1ß was determined by local intrauterine concentrations of P4 and E2. This study demonstrates that IL-1ß activates expression of mPGES-1 mRNA in uterine tissues to stimulate synthesis and secretion of PGE2 on days 10 to 13 of both pregnancy and the estrous cycle. The profile of COX-2 mRNA expression in the myometrium differs from its profile in the endometrium. This work provides new insight on the role of IL-1ß in PGE2 production to overcome luteolysis in pregnant pigs.

Effect of warm-rearing and heat acclimation on pituitary-gonadal axis in male rats.

Plasma gonadotrophic and testicular hormones concentrations in both immature and adult male rats exposed to 34 degrees C of ambient temperature were determined. In vitro steroidogenic ability of interstitial cells from experimental rats was also studied. Four groups of rats (n = 45) were used. Warm-reared (WR) males were housed in 34 degrees C and control-reared rats in 20 degrees C from birth to adulthood. The other groups were acclimated to 34 degrees C [warm-acclimated (WA) group] or 20 degrees C [deacclimated (DA) group] as adults. Decreased body weight and testis weight (p < 0.05) was found in heat-exposed groups, but relative testis weight was unchanged in WA and increased (p < 0.05) in WR and DA males. Plasma luteinizing hormone (LH) concentration increased in WA and DA males. Increased (p < 0.05) follicle-stimulating hormone (FSH) and prolactin plasma levels were found in DA and WR groups respectively. WA males had decreased testosterone (T) and WR rats androstenedione (A(4)) plasma concentration (p < 0.05). Interstitial cells (43% of them were Leydig cells by 3beta-hydroxysteroid dehydrogenase activity) from heat-exposed males secreted less (p < 0.05) T compared with the control group when incubated without LH (basal conditions). Androstenedione secretion decreased (p < 0.05) in WA rats. Secretion of estradiol-17beta (E(2)) was higher in WR and lower in DA cells under basal conditions. Weaker responsiveness to LH was observed in WR cells. Androgen synthesis from pregnenolone by interstitial cells increased (p < 0.05) in the WA group. We concluded that heat exposure of neonatal and adult male rats caused different pituitary-testicular axis adjustments. It seemed that long-term heat exposure of neonatal rats is less deleterious concerning the activity of pituitary-testicular axis than heat acclimation of adults.

The effect of progesterone on oxytocin-stimulated intracellular mobilization of Ca2+ and prostaglandin E2 and F2alpha secretion from porcine myometrial cells.

UNLABELLED: Our past studies have shown that porcine myometrium produce prostaglandins (PG) during luteolysis and early pregnancy and that oxytocin (OT) and its receptor (OTr) support myometrial secretion of prostaglandins E2 and F2alpha (PGE2 and PGF2alpha) during luteolysis. This study investigates the role of intracellular Ca2+ [Ca2+]i as a mediator of OT effects on PG secretion from isolated myometrial cells in the presence or absence of progesterone (P4). Basal [Ca2+]i was similar in myometrial cells from cyclic and pregnant pigs (days 14-16). OT (10(-7)M) increased [Ca2+]i in myometrial cells of cyclic and pregnant pigs, although this effect was delayed in myometrium from pregnant females. After pre-incubation of the myocytes with P4 (10(-5)M) the influence of OT on [Ca2+]i)was delayed during luteolysis and inhibited during pregnancy. Myometrial cells in culture produce more PGE2 than PGF2alpha regardless of reproductive state of the female. OT (10(-7)M) increased PGE2 secretion after 6 and 12 h incubation for the tissue harvested during luteolysis and after 12 h incubation when myometrium from gravid females was used. In the presence of P4 (10(-5)M), the stimulatory effect of OT on PG secretion was diminished. IN CONCLUSION: (1) porcine myometrial cells in culture secrete PG preferentially during early pregnancy and produce more PGE2 than PGF2alpha, (2) OT controls myometrial PGF2alpha secretion during luteolysis, (3) release of [Ca2+]i is associated with the influence of OT on PG secretion, and (4) the effects of OT on PG secretion and Ca2+ accumulation are delayed by P4 during luteolysis and completely inhibited by P4 during pregnancy.

Expression of enzymes of cyclooxygenase pathway and secretion of prostaglandin E2 and F2alpha by porcine myometrium during luteolysis and early pregnancy.

UNLABELLED: Past studies of uterine prostaglandin (PGs) and pig reproduction have focused on endometrial rather than myometrial PGs. This study documents the synthesis and secretion of myometrial prostaglandins (PGs) in pigs and the involvement of oxytocin (OT) in these processes. Cyclooxygenase-2 (COX-2) expression was similar in myometrial explants from cyclic and pregnant pigs (days 14-16) and OT (10(-7) M) in vitro significantly increased COX-2 protein regardless of reproductive state. Basal expression of prostaglandin E2 synthase (PGES) was higher during pregnancy than during luteolysis. Conversely, prostaglandin F synthase (PGFS) was highest during luteolysis and lower in myometrium from gravid animals. OT had no influence on the expression of PGES and PGFS. In another tissue culture experiment, myometrial slices produced more PGE2 than PGF2alpha regardless of reproductive state of the female. OT stimulated PGE2 production in myometrium harvested during luteolysis and increased PGF2alpha production in all tissues examined. Progesterone (P4; 10(-5) M) blocked stimulatory effect of OT on myometrial PG release. Myometrial OTr mRNA was higher (P=0.03) during luteolysis than during pregnancy. IN CONCLUSION: (1) oxytocin increases myometrial COX-2 expression, but does not influence the expression of terminal enzymes of PGs synthesis (PGES and PGFS); (2) porcine myometrium preferentially produces PGs during early pregnancy and secretes more PGE2 than PGF2alpha; (3) myometrial OT and OTr support secretion of PGs from myometrium during luteolysis.

The concentrations of catecholamines and oxytocin receptors in the oviduct and its contractile activity in cows during the estrous cycle.

UNLABELLED: In vitro experiments on oviducts of cyclic cows were undertaken to study: (1) the content of dopamine (DA), noradrenaline (NA) and adrenaline (A) in infundibulum, ampulla and isthmus, (2) the concentration of oxytocin receptors (OTR) in oviductal tissues and (3) the motility of ampulla and isthmus. Changes of DA content were observed in the infundibulum and the ampulla with maximal values occurring on Days 6-10 of the estrous cycle. The mean NA content was greatest in infundibulum

Endotoxaemia does not limit heat tolerance in rats: the role of plasma lipoproteins.

Severe hyperthermia disrupts the intestinal barrier, allowing bacterial lipopolysaccharides (LPS) to enter the bloodstream. Since the symptoms of heat stroke resemble those of endotoxic shock, there is a common belief that endotoxaemia induces heat stroke. Therefore, we studied the effects of different doses, from moderate to sublethal, of Escherichia coli LPS and an antipyretic (indomethacin) upon the temperature equilibrium of the brain and body of rats exposed to a constant ambient temperature of 38 degrees C. The animals were then heated until they developed heat stroke, which was identified using a critical thermal maximum (CTM) behavioural test. In separate experiments on defence against endotoxaemia, we compared plasma lipid composition in rats exposed to a sublethal dose of LPS, hyperthermia and heat stroke. Neither LPS nor indomethacin, injected into rats while they were in a hyperthermic steady-state condition of 40-41 degrees C, influenced their thermal equilibrium. Unexpectedly, moderate doses of LPS significantly elevated the thermal tolerance of rats, such that the mean (SEM) CTM value of body temperature was raised from 42.7 (0.3) degrees C to 43.1 (0.1) degrees C (P < 0.05). Indomethacin and huge doses of LPS failed to induce any change in this parameter. The sublethal dose of LPS did not induce mortality in rats subjected to heat stroke. Hyperthermic steady-state conditions and heat stroke alone significantly decreased plasma concentrations of cholesterol, triglyceride and high-density lipoproteins, while the concentrations of low-density lipoproteins increased. A similar pattern of changes was recorded in normothermic rats injected with a sublethal dose of LPS. In conclusion, endotoxaemia in heat-stressed rats induces neither a secondary increase in their core temperature nor a decrease in their ultimate thermal tolerance. Low-density lipoproteins are likely to protect heat-stressed animals against endotoxin-induced death.

Behavioral approach to the study of the upper limit of temperature tolerance in rats.

A simple test of critical thermal maximum (CTM) to assess a break-down of heat-escape behavior in rats is described. Experiments were performed on 18 unrestrained adult Wistar rats of both sexes. Hypothalamic and intraperitoneal (i.p.) temperatures as well as motor activity were simultaneously and continuously recorded in the rats exposed to heat. When animals were growing restless, as evidenced by an increase in their motor activity, which was usually recorded at hypothalamic temperatures well above 41 degrees C, we started testing CTM. To assess heat-escape behavior we used a precooled cooling bar (a part of a camp-cooler) which was placed at intervals in a climatic chamber. The hyperthermic rats, given the bar for 30 s, mounted it vigorously until they failed at particular levels of brain and body temperatures which were recognized as respective CTM values. Rapid external cooling of rats prevented lethal effects of the heat exposure. We were able to show effects of timing of heat exposure on heat tolerance. We also managed to detect small but significant differences in heat tolerance of warm-reared (an increase), cold-reared (a decrease), and bacterial-endotoxin-treated (an increase) rats. The heat-escape behavior was less heat-resistant than selective brain cooling response which was still present at CTM point. In conclusion, our CTM test is a safe and reliable way to study heat tolerance in rats.

[The development of Ascaris suum eggs in the presence of moxidectin]. / Rozwój jaj Ascaris suum w obecnosci moksydektyny.

The development of Ascaris suum eggs maintained in the culture containing moxidectin (Cydectin, Cyanamid) in concentration 1, 5, 25, and 50 micrograms/ml was studied. The abnormalities and slowing down of the rate of eggs development, depending on the drug concentration, were observed. Exposure of eggs to moxidectin in concentration 1 and 5 microgram/ml resulted in one- or two-week delay of development. In the higher concentration of moxidectin (25 micrograms/ml) only 18% of eggs became invasive. In the presence of 50 micrograms/ml of the drug only few eggs developed to invasive stage after 7 weeks. The development of embryons was stopped more often in the blastula or gastrula stage. The drug's solvent in the highest concentration restricted the development of Ascaris eggs by about 10%. Unembryonated eggs of the worm appeared to be unaffected by 50 micrograms/ml of moxidectin treatment lasting 1-4 days, but for slowing down a little the development rate. The same concentration of the drug in the culture during the first four days of development resulted in 20% reduction of invasive stage in comparison to the control.

[The effect of cydectin on the survival of second stage larvae and mature Ascaris suum cultured in vitro]. / Wplyw Cydectinu na przezywalnosc larw drugiego stadium oraz osobników doroslych Ascaris suum w hodowli in vitro.

Larvae of Ascaris suum (L2) newly hatched from eggs with sodium hypochlorite, were placed (2000 larvae per 2 ml) of culture in EAGLE's medium, containing 10% calve serum or without it. Moxidectin (Cydectin) was introduced into medium in concentrations: 5, 10, 25 and 50 micrograms/ml. The cultures were incubated for 3 days, and there were controlled every 12 hours. The effect of drug on survival of larvae was slightly expressed. After 3 days survival rates were 87, 81, 80 and 78% in medium with serum, respectively to moxidectin concentrations. The lethality of larvae was higher in medium without serum, and amounted to 17, 23, 29 and 31% in comparison with control probe after 72 hours. Adult Ascaris were placed on ARS medium with glucose (0.1%) containing moxidectin in concentrations 1, 5, 50 and 100 micrograms/ml. The worms' condition was examined every day based on motility and turgor of their body. After 14 days of incubation in control probe 50% worms were alive, but their vitality was reduced. The behaviour of Ascaris in the presence of 50 micrograms/ml moxidectin was similar to those from the control. Only the highest concentration of drug (100 micrograms/ml) was lethal in 100% on the 8th day. The lower moxidectin concentrations (1 and 5 micrograms/ml) were not lethal to adult worms, they had even the positive effect on survival rate and condition of adult Ascaris. The eggs laid by females which were maintained in culture with drug were collected. There were no disturbances in their future development.