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Biomedical subjects

D W Forrest

Publications and source records attributed to D W Forrest.

At least 37 records · Page 2Linked to original sources

Ethanol alters vasoactive intestinal peptide-induced steroid release from immature rat ovaries in vitro.

The present study was conducted to examine the acute effects of ethanol (ETOH) on basal and VIP-induced release of testosterone (T) and estradiol (E2) from immature ovaries in vitro. Ovaries were collected from anestrus (A) and both naturally occurring and pregnant mare's serum gonadotropin (PMSG)-induced early proestrus (EP) animals. The ovaries were incubated in either media alone, media plus 1 microM VIP, media plus ETOH in doses ranging from 25 to 100 mM, or media plus each dose of ETOH containing VIP. The present results demonstrate that ETOH did not affect either basal or VIP-induced steroid release from ovaries collected from A animals. Likewise, the ETOH did not alter basal steroid secretion from EP animals; however, the drug significantly reduced the VIP-stimulated release of both T and E2 from EP ovaries. Thus, these data demonstrate for the first time that ETOH is capable of altering prepubertal ovarian responsiveness to VIP, a peptide known to be involved in the developmental regulation of ovarian function.

Animals↗

Suckling inhibits release of luteinizing hormone-releasing hormone from the bovine median eminence following ovariectomy.

The effect of suckling on depletion of hypothalamic LHRH from the median eminence (ME) following ovariectomy (OVX) was determined in cattle. Multiparous, postpartum Holstein cows were assigned randomly to three groups: intact, nonsuckled (INT, n = 4); ovariectomized (3 to 5 d after parturition), nonsuckled (OVX, n = 4); and ovariectomized (3 to 5 d after parturition) and suckled by three calves (OVX-S, n = 5). Blood samples were collected at three periods (1 to 7 d before parturition and 3 to 5 d and 31 to 37 d after parturition) to determine plasma LH concentration. At 31 to 37 d after parturition, all cows were slaughtered and each ME was collected and mid-sagitally sectioned. The left half of each ME was used to determine content and concentration of LHRH. Concentrations of LH and LHRH were determined by RIA. Plasma LH concentration was similar among the three groups at 1 to 7 d before parturition and 3 to 5 d after parturition; however, at 31 to 37 d after parturition, OVX cows had a greater (P less than .05) concentration of LH (2.25 +/- .64 ng/ml) than either INT (.47 +/- .10 ng/ml) or OVX-S (.92 +/- .14 ng/ml) cows. Content of LHRH in the ME of INT (80.12 +/- 15.0 ng) and OVX-S 109.8 +/- 16.4 ng) cows was similar but was greater (P less than .05) than that in OVX cows (48.95 +/- 5.9 ng).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Biological and immunological luteinizing hormone activity and blood metabolites in postpartum Brahman cows.

Multiparous Brahman cows were assigned by order of calving and sex of calf to groups to be fed to maintain body condition score (BCS) of 6 or greater (M; n = 10) or to lose BCS (L; n = 10). Blood samples were collected weekly for progesterone analysis and at 15, 30 and 45 d after parturition at 15-min intervals for 6 h for determination of immunological (ILH) and biological (BLH) luteinizing hormone. Serum concentrations of ILH were determined using a double antibody RIA procedure, whereas BLH was determined using a rat interstitial cell-testosterone bioassay (RICT). By 45 d after parturition 7 of 10 M cows had returned to estrus. Therefore, comparisons between groups were made on d 15 and 30 postpartum. Cows in the M group had a shorter (P less than .001) interval to first estrus (46.7 d) than did L cows (91.2 d). The concentrations of bioactive and immunoactive LH were parallel between d 15 and 30 postcalving. However, a day x treatment interaction (P less than .05) showed that episodic BLH concentrations (ng/ml) decreased with day postpartum in L, but increased in M cows from d 15 to 30 postcalving. Likewise, relative biological activity, as measured by B:I ratios, decreased between d 15 and 30 in L cows, whereas it increased in M cows during the same period (B:I x day interaction; P less than .05).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Biological activity of LH during the peripartum period and the estrous cycle of the ewe.

Biological activity of luteinizing hormone (LH) is related to the degree of glycosylation of the glycoprotein hormone. The objectives of this study were to determine changes in biologically (BLH) and immunologically (ILH) active LH concentrations in plasma (in vitro bioassay and radioimmunoassay, respectively) and in the ratio of BLH to ILH (B:I) during the peripartum period and during the estrous cycle of the ewe. Blood samples were collected daily 4 days before through 4 days after parturition and during one estrous cycle. Also, samples were collected at 15-min intervals for 6 hr on Days 3 and 12 of the estrous cycle to quantify the influence of an elevated plasma concentration of progesterone (P) on the episodic secretion profiles of BLH. Progesterone concentration was determined on the 4th days pre- and post-partum, on each day of the estrous cycle and at hourly intervals on Days 3 and 12 of the cycle to investigate the hypothesis of an inverse relationship between P and BLH. The BLH and ILH concentrations were low during the peripartum period, and the B:I ratio did not increase by the 4th day postpartum. Mean ILH concentration was greater (P less than .05) in the postpartum than during the prepartum period. During the estrous cycle, mean daily B:I ratio was consistently above unity except for the day of estrus. The pre-ovulatory LH surge (BLH and ILH) was associated with a decrease (P less than .05) in the mean B:I ratio to 0.0065. Mean concentrations of BLH and ILH in plasma samples collected every 15 min on Day 12 were similar to Day 3 of the cycle.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Ovarian inhibition of peripheral plasma concentration of follicle stimulating hormone in prepuberal Holstein heifers.

The objective of this study was to determine effects of age and castration on follicle stimulating hormone (FSH) secretion in prepuberal heifers. In experiment 1, twelve heifers were bilaterally ovariectomized at 3, 6, or 9 months of age (n = 4/group). Blood was collected at 10 min intervals for 8 hr at 1 week before ovariectomy and 1 and 4 weeks after ovariectomy. Frequency, amplitude and duration of FSH pulses were calculated. Mean plasma concentration of FSH (ng/ml), and frequency (pulses/8 hr), amplitude (ng/ml), and duration (min/pulse) of FSH pulses were not altered by age. Mean concentration of FSH increased (P less than .01) from 1 week before to 1 week and 4 weeks after ovariectomy, respectively, in all age groups. Pulse frequency increased (P less than .05) from 1 week before ovariectomy to 4 weeks after ovariectomy in 3 month old heifers, from 1 week before to 4 weeks after ovariectomy in 6 month old heifers, and from 1 week before to 1 week and 4 weeks after ovariectomy in 9 month old heifers. In experiment 2, twelve heifers were bilaterally ovariectomized at 3, 6 or 9 weeks of age (n = 4/group). Sample collection and measurement of mean concentration of FSH were the same as in experiment 1. Mean concentration of FSH increased (P less than .01) from 1 week before to 1 and 4 weeks after ovariectomy in heifers ovariectomized at 6 and 9 weeks of age.(ABSTRACT TRUNCATED AT 250 WORDS)

Aging↗

Effects of nutritional level and biological type on gonadotropin-releasing hormone-induced luteinizing hormone release and plasma progesterone, estrone and estradiol concentrations in pre- and post-partum beef heifers.

Forty-six beef heifers (16 to 23 mo) of two biological types (small = Red Poll-sired, large = Charolais-sired) were individually fed from d 90 of gestation through parturition to evaluate the effects of nutritional restriction on plasma LH and steroid hormone concentrations. Heifers were allotted to one of two nutritional treatments to achieve a BW reduction (loss, fed at 1% of BW/d) or to maintain initial BW (maintenance, fed 1.5% of BW/d) to parturition. Gonadotropin-releasing hormone (100 micrograms) was injected i.m. three times during gestation (d 130; d 200; d 270) and twice after parturition (d 1 to 14; d 23 to 36). Blood samples were collected at 20-min intervals after GnRH for 4 h. Maternal BW change from d 90 to parturition differed (P less than .01) between loss and maintenance heifers. Mean plasma progesterone concentrations were greater (P less than .05) at d 130 and 270 of gestation in small than in large heifers and were greater (P less than .01) at d 23 to 36 postpartum in maintenance than in loss heifers. Mean concentrations of estrone and estradiol were greater (P less than .05) in large than in small heifers at d 200 of gestation. Mean plasma LH concentrations following GnRH injection were greater (P less than .01) in loss than in maintenance heifers at 200 and 270 d of gestation. Metabolizable and retained energy were related inversely to LH release during mid and late gestation.(ABSTRACT TRUNCATED AT 250 WORDS)

Animal Nutritional Physiological Phenomena↗

Gonadotropin-releasing hormone-induced luteinizing hormone release in heifers: effect of nutrition during gestation.

The effects of nutrition during the last two trimesters of gestation on GnRH-induced LH release were assessed in crossbred heifers. Heifers (n = 58) were allotted at 90 d gestation to one of three levels of an experimental diet fed at 1, 1.5 or 2% of BW to attain maternal BW loss, BW maintenance or BW gain, respectively, at parturition. Twenty-two heifers were injected (i.m.) once with 100 micrograms GnRH between d 14 and 1 before parturition, and 32 heifers were injected (i.m.) once with 100 micrograms GnRH between d 8 and 21 after parturition. Jugular blood samples were collected before and at 30-min intervals after GnRH for 4 h. Least squares means for BW change differed (P less than .01) among BW loss (-17.6%), BW maintenance (-6.0%) and BW gain (7.0%) heifers. Basal plasma LH concentration was not influenced by nutritional treatment and was similar before and after parturition for all groups. However, in response to GnRH, peak plasma LH concentration was greater (P less than .10) for prepartum than for postpartum heifers. Mean LH peak amplitude in prepartum heifers was approximately twofold greater (P less than .10) in the BW loss and maintenance groups compared with the BW gain group. Prepartum LH release was related inversely (r = -.64) to change in heifer BW and increased (P less than .01) as BW loss increased during gestation. After parturition, mean LH peak amplitude and area under the response curve averaged 50% less (P less than .10) in the BW loss and maintenance groups than in the BW gain group.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Methods for collecting follicular oocytes from mares.

A series of experiments was conducted to develop a procedure for consistent, repeatable collection of oocytes from the preovulatory follicle of the mare. In one experiment, in situ follicular aspiration with a needle and syringe was performed on 19 mares. From 37 aspirations, four oocytes were recovered (10% recovery rate). In a second experiment, ovaries were visualized via standing flank laparotomy during which two different aspiration techniques were used. Use of a needle and syringe as in the first experiment resulted in successful oocyte recovery in one of seven (14%) attempts. Aspiration via a continuous irrigation vacuum system (CIV), developed for use during laparotomy, resulted in collection of oocytes from six of 10 (60%) attempts. In the third experiment, oocytes were recovered from seven of 18 (38%) attempts at in situ follicular aspiration using a double-lumen needle attached to the CIV. In each experiment, some mares were subjected to stimulation of follicular maturation by exogenous hormones. Oocyte recovery was significantly increased in treated mares as compared with nontreated mares. Results indicate that collection of equine follicular oocytes by in situ aspiration is possible with moderate success. Oocytes apparently are not physically damaged by the procedure, as most retained either the corona radiata or the entire cumulus cell mass.

Journal Article↗

Gestation nutrition, tissue exchange and maintenance requirements of heifers.

Forty-six pregnant, crossbred, 2-yr-old heifers of large or small mature size were individually fed a 70% cottonseed hull diet during gestation. Heifers were fed at either 1.0% (nutritionally restricted) or 1.5% (nonrestricted) of body weight from 90 d gestation through parturition. Live weight, from 90 d gestation to parturition, was reduced by 20.5% and 1.0% for restricted and nonrestricted heifers, respectively. Whereas nonrestricted heifers gained maternal protein (3.2 kg) from d 90 through parturition, restricted heifers lost (P less than .05) protein (-5.4 kg) and mobilized twice (P less than .05) as much fat (49 vs 25 kg). Percentage of empty body protein increased 13.1 and 9.3% in restricted and nonrestricted heifers, respectively, whereas fat decreased (P less than .05) 31.7% (restricted) and 23.5% (nonrestricted) from 90 d to parturition. Daily metabolizable energy for maintenance (MEm) was greater for large than for small mature size heifers (169 vs 158 kcal/kg.75). Efficiency of ME use for gain was greater for small than for large mature size heifers (36.5 vs 31.2%). Efficiency in early gestation (45.4%) was greater than in late gestation (29.4%) and averaged 33.8% for 90 d gestation to parturition. Maintenance ME requirements increased 25% and efficiency of ME use decreased 35% with advancing stage of gestation. Nutritional restriction of heifers reduced (P less than .05) calf birth weight (27.3 vs 30.2 kg) and decreased gestation lengths (275 vs 282 d) compared with nonrestricted heifers. This research indicates that nutritional restriction of beef heifers alters birth weight, repartitions maternal tissues and changes rate of tissue mobilization.

Animals↗

Biological activity of luteinizing hormone in the peripartum cow: least activity at parturition with an increase throughout the postpartum interval.

The biological (B) and immunological (I) activities of luteinizing hormone (LH) were determined during four peripartum periods in the cow. The sampling periods were PRE-5 (approximately 5 days prior to parturition), POST-3 (Day 2 or 3 postpartum), POST-12 (Day 11 or 12 postpartum) and LUTEAL (Day 11 or 12 following the first observed postpartum estrus). Blood samples were collected at 10-min intervals for either 8 h (PRE-5, POST-3, and POST-12) or 6 h (LUTEAL). Four hours prior to the end of each sampling period, 100 micrograms of luteinizing hormone-releasing hormone (LHRH) was injected i.v. Plasma concentrations of LH were analyzed by a validated bioassay (rat interstitial cell testosterone) and a radioimmunoassay. Area under the LHRH-induced LH release curve was calculated by the trapezoidal rule, and endogenous LH was determined by averaging the pre-LHRH treatment values. Paired t-analyses were used to compare LH release between periods. The periods of lowest (p less than 0.05) bioactive LH (BLH) were PRE-5 and POST-3. During POST-12, BLH was maximal. Endogenous immunoactive LH (ILH) was maximal during the POST-12 period, with PRE-5, POST-3, and LUTEAL being the least (p less than 0.05). The B:I ratio was lowest (p less than 0.05) around the time of parturition (PRE-5 and POST-3), then increased (p less than 0.05) by Day 12 postpartum. The ratio then increased (p less than 0.05) again by the LUTEAL period. These data suggest that the biological quality of LH changes throughout the puerperium. We infer from these data that the low biological activity of LH (subquality LH) may contribute to the postpartum infertility in the cow.

Animals↗

Reproductive performance of postpartum beef cows after short-term calf separation and dietary energy and protein supplementation.

Beef cows (n = 294) calving between November and April in six states were used to evaluate the effects of postpartum diet and calf separation on body weight, body condition score (BCS), reproductive performance, and weaning weight of calves. In each state, half of the 48 cows that calved during 60 d were group fed an additional 4.5 kg of a 20% crude protein supplement daily for 28 d starting an average of 30 d post partum (flush). Calves were separated from half of the flush and half of the nonflush cows for 48 h at 14 and 28 d after the beginning of flush. Progesterone was quantified in plasma samples obtained weekly during a 56-d breeding period to assess ovarian luteal activity. The breeding period started at the first calf separation. BCS ranged from 3.3 to 5.6 among states (on a scale of 1 to 9) at the start of the flush but was similar for treatments within a state. There was a state x flush (P < 0.008) effect on body weight at the end of the flush period. Weaning weights were influenced by state x separation x flush (P < 0.06) and were greatest for flush nonseparated calves in five of six states. There were state x flush (P < 0.08) and separation (P < 0.04) effects on ovarian luteal activity at the start of the breeding period. Flush and separation tended to increase ovarian luteal activity. During the breeding period, ovarian luteal activity was influenced only by state but there was a state x separation x flush effect (P < 0.001) on the number of weeks post partum to onset of ovarian luteal activity. Conception rate and days postpartum to conception were not influenced by either separation or flush but were affected by state (P < 0.001). These data indicate that flushing may increase weaning weights of calves and calf separation may hasten the onset of postpartum ovarian luteal activity, but conception rate and days postpartum to conception for cows in thin to moderate body condition were not influenced by the calf separation or flushing treatments.

Journal Article↗

Cloprostenol inouced luteal regression in the beef cow. I. Ovarian response and endocrine changes.

Forty-two cycling, multiparous beef cows (percentage-Brahman) were given two injections of 500 ug Cloprostenol (CLP) 11 days apart. Cows were randomly allocated to be ovariectomized at 0, 12, 24, 36, 48, 60 or 72 hr after the second CLP injection. Mean CL weight declined within 36 hr after CLP. Mean concentration of P4 in luteal tissue increased between o and 60 hr, while mean P4 content per CL declined by 12 hr after CLP. There was a precipitous decrease in mean serum P4 by 12 hr following CLP injection. Serum E2 was elevated until 24 hr and then declined through 72 hr after CLP. Follicular T concentration increased from 0 to 48 hr and then decreased by 60 hr. We conclude that CLP caused rapid diminution of luteal function which was accompanied by a reduction in P4 content but not in P4 concentration. Futhermore, the concentration of E2 in large follicles decreased by 72 hr post-CLP which is consistent with an alteration of the steroidogenic pathway in the periovulatory follicle.

Journal Article↗

Cloprostenol induced luteal regression in the beef cow. II. Histological evaluation of corpora lutea and correlation with luteal progesterone.

Forty-two cycling, multiparous beef cows (percentage-Brahman) were injected twice at 11-d intervals with 500mug Cloprostenol (a prostaglandin F(2alpha) analog) to induce luteolysis. Cows were randomly assigned for ovariectomy at 12 hr intervals from 0 to 72 hr post-injection. Corpora lutea were excised and one-half of the corpus luteum was stored in phosphate-buffered formalin until mounting and staining with hematoxylin and eosin. The other half of the CL was snap-frozen for determination of progesterone content and concentration. Luteal cell density increased following Cloprostenol injection and was significantly correlated with a shift from predominantly healthy Type I cells to predominantly degenerating Types III and V cells. Cell mitosis tended to decrease by 12 hr and was lower by 24 hr post-injection. Cell pyknosis increased by 24 hr post-injection and was correlated with the decrease in percentage of healthy luteal cells. No pattern was detectable in cell karyorrhexis. Histological regression of the CL was inversely correlated with CL progesterone content. Therefore, we conclude that a reduction in cell mitosis is the earliest morphological sign of degeneration of the CL and that the CL follows a well-defined sequence of regression which is accompanied by a decrease in progesterone content.

Journal Article↗

The influence of exogenous estradiol on bobwhite quail (Colinus virginianus) reproductive systems.

Mean plasma 17-beta-estradiol (E2) concentrations of nonphotostimulated adult bobwhite quail were less than 31.2 and 119.9 pg/ml for males and females, respectively. Dietary beta-estradiol-3-benzoate (E2 beta) dosages of 10, 100 or 500 micrograms/bird/day caused mean plasma E2 concentrations of females to increase by 1.2, 2.0 or 5.6 times. Oviduct weights were significantly increased in females fed E2 beta dosages of greater than 100 micrograms/bird/day for five days. Gonad weights were not significantly effected in either sex. Ten- to fifty-fold greater doses of dietary E2 beta were required to induce oviduct growth responses equivalent to those produced by injected E2 beta.

Animals↗

The concentration of estradiol-17 beta in bovine semen.

This study was conducted to evaluate the influence of age, breed, epididymectomy and semen processing on the concentration of estradiol-17 beta (E2) in bovine semen. Semen was collected either by electroejaculation or with an artificial vagina. Neat semen samples were stored at -20 C until analysis. Processed, frozen semen and an egg yolk-citrate semen extender were obtained from a commercial semen processing firm and stored in liquid nitrogen at -196 C. The concentration of E2 in semen was determined by radioimmunoassay. Semen from mature (greater than 24 mo), fertile Brahman (n = 19), Brangus (n = 16), Charolais (n = 29), Holstein (n = 15) and Santa Gertrudis (n = 25) bulls was analyzed for E2 concentration, and no difference (P greater than .10) between breeds was found. There was no difference (P greater than .10) in seminal E2 concentration between mature, fertile bulls (n = 104) and epididymectomized bulls (n = 22). In semen collected from prepuberal (12 to 16 mo, n = 21), peripuberal (17 to 20 mo, n = 17) and mature (greater than 24 mo, n = 19), Brahman bulls, the mature bulls had a lower (P less than .01) semen E2 concentration than peripuberal and prepuberal bulls. There were no differences (P greater than .10) in seminal E2 concentration among peripuberal Angus (n = 8), Hereford (n = 8) and Brahman (n = 17) bulls.(ABSTRACT TRUNCATED AT 250 WORDS)

Age Factors↗

Reproductive response to suckling manipulation in Spanish goats.

One hundred and fifty-six Spanish does were used to evaluate the effect of suckling manipulation on postpartum breeding. Does were divided into four herds dependent upon their kidding dates (range from October to January) and location. All kids were nursed ad libitum for approximately 30 days following birth. Groups were then subdivided, and does with kids were randomly allotted to one of the following treatment groups: 1) continuous suckling (CS), 2) once-daily suckling (ODS) or 3) early weaning (EW). Nonlactating does (NL) which lost a kid or aborted were also evaluated for rebreeding performance. At least one fertile male equipped with a marking harness was placed with each treatment group for estrus detection. After 30 days, ODS kids were returned to their dams. The proportion of does exhibiting estrus within 60 days postpartum was greater for ODS and EW does compared to CS does (P<0.05 and P<0.001, respectively). Postpartum interval to first estrus was shorter (P<0.05) for ODS does than for CS does (41.7 and 48.0 days, respectively). The percentage of does conceiving within 60 days postpartum was 25.0, 44.7, 74.4 and 70.7% for CS, ODS, EW and NL does, respectively. The interval from parturition to conception was shorter (P<0.05) for ODS does (43.6 days) than for CS does (50.4 days). Overall kid production was 1.87 kids/doe/year. These results indicate that reducing the suckling stimulus in Spanish does during the breeding season may result in an earlier return to estrus with a greater percentage of does rebreeding within 60 days postpartum.

Journal Article↗