Effects of interferon-tau and interferon-alpha on proliferation of bovine endometrial cells.

The ruminant conceptus secretes a unique interferon, interferon-tau, that regulates endometrial prostaglandin secretion during early pregnancy. Because one of the pleiotropic effects of interferons is to inhibit cellular proliferation, a series of experiments was conducted to determine whether or not the bovine endometrium is sensitive to the antiproliferative effect of interferon-tau and the related interferon, interferon-alpha. Endometrial epithelial and stromal cells were prepared from the endometrium of cows from Days 11-17 after estrus and incubated with recombinant bovine interferon-tau (rbIFN tau; 1-1000 ng/ml), recombinant bovine interferon-alpha 1 (rbIFN alpha; 1-1000 ng/ml), recombinant human interferon-alpha 2b (rhIFN alpha; 100 ng/ml), or ovine interferon-tau (oIFN tau; 100 ng/ml). Proliferation was determined by monitoring uptake of [3H]thymidine into DNA. Generally, interferons did not inhibit proliferation of endometrial epithelial cells. Exceptions were for 1000 ng/ml rbIFN tau, which inhibited proliferation by 23%; 100 ng/ml rbIFN alpha, which inhibited proliferation by 28% in one of two experiments only; and 100 ng/ml oIFN tau, which inhibited proliferation by 17%. Proliferation of endometrial stromal cells was not inhibited by any concentration of any interferon in two separate experiments. Therefore, unlike other bovine cells tested previously (lymphocytes and oviductal cells), bovine endometrial cells were not consistently inhibited by IFN tau or IFN alpha. Such reduced responsiveness of endometrial cells to the antiproliferative effects of type I interferons could allow for growth of the endometrium during the period of pregnancy when the conceptus produces IFN tau.

Responses of bovine lymphocytes to heat shock as modified by breed and antioxidant status.

We tested whether resistance of lymphocytes to heat stress is modified by breed, intracellular glutathione content, and extracellular antioxidants. In the first experiment, lymphocytes from Angus (Bos taurus, non-heat-tolerant), Brahman (B. indicus, heat-tolerant), and Senepol (B. taurus, heat-tolerant) heifers (12 heifers per breed) were cultured at 45 degrees C for 3 h to evaluate thermal killing, at 42 degrees C for 12 h in a 60-h phytohemagglutinin-induced proliferation test, and at 42 degrees C for 1 h to measure induction of heat shock protein 70 (HSP70). Killing at 45 degrees C was affected by breed x temperature (P < .01); the decrease in viability caused by a temperature of 45 degrees C was greater for Angus than for Brahman or Senepol. For phytohemagglutinin-stimulated lymphocytes, heating to 42 degrees C reduced [3H]thymidine incorporation equally for all breeds. Viability at the end of culture was affected (P < .001) by a breed x temperature interaction because the decrease in viability caused by culture at 42 degrees C was greatest for lymphocytes from Angus heifers. Heat shock for 1 h at 42 degrees C caused a two- to threefold increase in intracellular concentrations of HSP70, but there was no interaction of temperature with breed. In another experiment (with lymphocytes harvested from three Holstein cows), buthionine sulfoximine, a glutathione synthesis inhibitor, inhibited (P < .01) proliferation of phytohemagglutinin-stimulated lymphocytes at 38.5 and 42 degrees C. Addition of the antioxidants glutathione or thioredoxin to culture did not reduce the effects of heating to 42 degrees C on proliferation.(ABSTRACT TRUNCATED AT 250 WORDS)

Photoperiod influences age at puberty of heifers.

Two experiments were conducted to determine if exposure of prepubertal heifers to supplemental lighting hastens the onset of puberty. In Exp. 1, 16 heifers were paired according to birth date (April 21 to July 4) and assigned randomly to exposure to either 18 h light/d (L) or natural photoperiods (N) from 22 wk of age until puberty. Twenty-two heifers in Exp. 2, born between February 27 and March 31 and between May 3 and May 17, 1981, were exposed to L or N from 24 wk of age until March 23, 1982. In Exp. 2, animals were bred at all estrous periods until conception. Age at first ovulation and first estrus were less (P less than .01 for Exp. 1 and P less than .10 for Exp. 2) for L than N heifers. Average ages at first estrus were 318 (L) and 367 d (N) for Exp. 1 and 367 (L) and 394 d (N) for Exp. 2. Age at conception in Exp. 2 was similar for L (380 d) and N (396 d) groups. There were no significant differences between L and N heifers in changes in body weight for either experiment. There was a photoperiod X age interaction (P less than .06) for ovarian volume in Exp. 1 because the rate of ovarian growth was greater for L than N heifers. Concentrations of LH were not affected by photoperiod in Exp. 1 and not measured in Exp. 2. There were no significant changes in LH concentrations between 22 and 34 wk of age. When expressed relative to first ovulation, LH levels were highest at 7 and 2 wk before first ovulation. Concentrations of prolactin in Exp. 1 were not significantly affected by photoperiod. It was concluded that supplemental lighting after 22 or 24 wk of age reduced ages at first ovulation and first estrus in heifers born from February to July. These effects of photoperiod were accompanied by changes in ovarian development.

The influence of photoperiod on the onset of puberty in the female rabbit.

Seventy-six New Zealand white does born between June 28, 1979 and April 6, 1980 were used in an experiment of 2 X 2 X 2 factorial design to determine if 1) exposure to 18 h (L) or 6 h (D) of light/d beginning at weaning influenced age and body weight at puberty and 2) if mating and(or) hormone treatment at puberty influenced ovulation rate and number of embryos. Beginning at weaning, estrus was checked daily using males known to be fertile. At first expression of estrus, does were either mated or nonmated and were injected iv with either 30 IU human chorionic gonadotropin (hCG), or saline. Means for the L and D groups for age at puberty (d), body weight at puberty (kg), ovarian weight (g) and number of embryos 5 d postcoitus were 105 +/- 3.6 vs 121.9 +/- 4.1 (P less than .01); 2.65 +/- .07 vs 2.87 +/- .08 (P less than .05); .56 +/- .04 vs .78 +/- .04 (P less than .001) and 6.1 +/- .83 vs 3.44 +/- .67 (P less than .01), respectively. Photoperiod did not influence number of ovulations. Number of embryos relative to number of ovulations were higher in rabbits exposed to 18 h of light. Does that were both mated and hormone-treated had more (P less than .025) corpora lutea (11.0 +/- .9) than does that were either hormone-treated (7.7 +/- .86) or mated (7.0 +/- .97) only. Mated does had heavier uteri (10.8 +/- .5 vs 7.9 +/- .5) while hormone treatment increased both ovarian and uterine weights (g) over nontreated does (.74 +/- .04 vs .59 +/- .05; 9.9 +/- .45 vs 8.8 +/- .65). Multiple regression analysis revealed that does born in summer reached puberty later than those born during other seasons. It was concluded that season of birth and exposure of does to 18 h of light from weaning affect onset of puberty. Increasing daily light exposure from 6 to 18 h/d may improve litter size in pubertal does.

Influence of season on sexual development in heifers: age at puberty as related to growth and serum concentrations of gonadotropins, prolactin, thyroxine and progesterone.

An experiment was done to test the hypothesis that seasonal changes in environment during the first and second 6 months of life influence age at puberty in heifers. Twenty-eight Angus X Holstein heifers, born in March (M) or September (S), were reared under natural conditions until 6 months of age. From 6 to 12 months of age, heifers were reared in environmental chambers programmed to simulate seasonal changes in temperature and photoperiod characteristic of spring, summer and early autumn (Sp-F chamber) or autumn, winter and early spring (F-Sp chamber). S were younger (P less than 0.06) at puberty than M, and Sp-F were younger (P less than 0.08) than F-Sp for both M and S. Mean ages at puberty were 295 for S, Sp-F; 319 for S, F-Sp; 321 for M, Sp-F and 346 days for M, F-Sp. Average daily gain (ADG) between 6 and 9 months of age [1.03 kg/day (S) vs. 0.91 kg/day (M)] and mean concentrations of serum luteinizing hormone (LH) between 6 and 7 months of age [3.45 ng/ml (S) vs. 0.47 ng/ml (M)] were greater (P less than 0.01) for S than M, suggesting an association between these traits and date of birth effects on age at puberty. Differences in these traits did not seem to be involved in the chamber effect on age at puberty, since ADG from 6-9 months of age was greater (P less than 0.05) for F-Sp heifers and chamber did not generally affect LH concentrations. Serum concentrations of follicle-stimulating hormone (FSH) were not significantly influenced by month of birth or chamber, but concentrations tended to decrease with age. Serum concentrations of thyroxine (T4) were higher in M than S at 6 months of age (7.8 micrograms/dl vs. 6.3 micrograms/dl) but not at other times, and chamber did not have a significant affect. Prolactin (Prl) concentrations paralleled patterns of temperature and day length and did not appear to be related to age. Although cattle are not seasonal breeders, these results demonstrate that season of birth and season of attainment of puberty influence age at puberty in heifers. Season may have influenced age at puberty by affecting serum concentrations of LH or Prl, or growth rate.

The effect of photoperiod on serum concentrations of luteinizing and follicle stimulating hormones in prepubertal heifers following ovariectomy and estradiol injection.

Eleven heifers, between 63 and 197 days of age, were exposed to 18 hr light/day (L) or natural photoperiods (N), beginning October 19, 1979. They were ovariectomized 8 weeks later. LH concentrations after ovariectomy were not affected by photoperiod, but the rate of increase of FSH after ovariectomy was greater (P<0.10) for group L than for group N. Three weeks after ovariectomy, heifers were injected, IV, with 0.1 mug/kg estradiol-17beta. LH concentrations initially decreased after injection. This was followed by a series of pulses larger than those prior to injection. FSH concentrations declined after injection and remained low throughout the sampling period. The net response of LH concentrations to estradiol (mean post-injection concentration minus mean pre-injection concentration) was greater (P=0.05) for group L (4.7+/-0.49 ng/ml) than for group N (2.9+/-0.37 ng/ml). Photoperiod did not affect the net response of FSH concentrations to estradiol. We concluded that exposing prepubertal heifers to 18 hr light/day during the winter resulted in a greater rate of increase of FSH after ovariectomy and greater estrogen-induced LH release. Because the response of LH to estradiol-17beta differed from the response of FSH, these hormones may be regulated differently.