M. Garcia-Winder
University of Nebraska–Lincoln
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Animal Reproduction Science | 1995
E. G. M. Bergfeld; F. N. Kojima; M. E. Wehrman; Andrea S. Cupp; K. E. Peters; V. Mariscal; T. Sanchez; Roger J. Kittok; M. Garcia-Winder; J. E. Kinder
Abstract The present study was designed to test whether progesterone from exogenous and endogenous sources modulates the frequency of luteinizing hormone (LH) pulses in a differential fashion. Our working hypotheses were: (1) the frequency of secretion of LH pulses and concentration of 17β-oestradiol in circulation would be directly related to circulating concentration of progesterone; (2) progesterone from an exogenous source would have a different effect on frequency of LH pulses and circulating concentration of 17β-oestradiol than progesterone from an endogenous source. Cows were treated with graded doses of PGF 2α or progesterone to result in varying concentrations of progesterone in circulation from endogenous and exogenous sources. Treatment with PGF 2α resulted in concentrations of circulating progesterone among animals in this group that ranged from 0.5 to 10.9 ng ml −1 of plasma. Treatment with progesterone resulted in circulating concentrations of progesterone among animals in this group that ranged from 0.8 to 11.8 ng ml −1 of plasma. Concentrations of progesterone in circulation and frequency of LH pulses were negatively correlated ( r = −0.59) in cows with functional corpora lutea and in cows treated with progesterone without corpora lutea ( r = −0.62). The frequency of LH pulses had the same relationship to the varying concentrations of progesterone in both treatment groups. Cows with higher progesterone levels had fewer LH pulses and cows with lower progesterone had a greater frequency of LH pulses. Mean circulating concentrations of 17β-oestradiol also had the same relationship with varying concentrations of progesterone in both treatment groups. Cows with higher progesterone levels had lower 17β-oestradiol and cows with lower progesterone had higher 17β-oestradiol levels. The results indicate that there is a direct relationship between circulating concentration of progesterone, frequency of LH pulses and circulating concentration of 17β-oestradiol. In addition, progesterone modulates the frequency of release of LH pulses from the pituitary and circulating concentration of 17β-oestradiol in a similar fashion when coming from either an endogenous or exogenous source.
Animal Reproduction Science | 2003
F.N. Kojima; E. G. M. Bergfeld; M. E. Wehrman; Andrea S. Cupp; K.E. Fike; D.V. Mariscal-Aguayo; T. Sanchez-Torres; M. Garcia-Winder; Debra T. Clopton; A.J. Roberts; J. E. Kinder
The objectives of the present study were to determine how varying frequency of LH pulses as controlled by varying treatments with progesterone (P4) in cattle would affect: (1) concentration of steroid hormones and activity of insulin-like growth factor binding proteins (IGFBPs) in the ovarian follicular fluid and blood plasma, and (2) duration of persistence of largest ovarian follicles. There were four treatment groups (n=7 per group) and a control group (n=5) of mature, non-lactating beef cows. Treatments were: (1) two progesterone releasing intravaginal devices (PRIDs) for 16 days (2PRID); (2) a half PRID for 16 days (0.5PRID); (3) two PRIDs for 8 days, then a half PRID for 8 days (2-0.5PRID); or (4) a half PRID for 8 days, then two PRIDs for 8 days (0.5-2PRID). Treatment was initiated on the fifth day of the estrous cycle, which was designated as Day 0, and continued for 16 days. All P4-treated females were administered prostaglandin F2alpha on Day 0 and 1 to regress their corpora lutea. Frequency of LH pulses was greater during treatment with the smaller dose of P4 compared with treatment with the larger dose of P4 and the control group. Ovarian follicles were classified into five categories based on ultrasonographic observations: growing (G); atretic (A); growing dominant (GD); growing persistent (GP); or atretic persistent (AP). At ovariectomy on Day 16, the largest and second largest follicles collected were re-classified into five categories based on follicular concentration of steroids. Classification of the largest follicle collected on Day 16 was influenced by treatment (P<0.005), with the 2PRID group having A follicles, the 2-0.5PRID group GP follicles, the 0.5-2PRID group AP follicles, and the 0.5PRID group GD and GP follicles. Concentrations of 17beta-estradiol (E2) were greatest in GD and GP follicles (P<0.05). There was less (P<0.05) activity of IGFBP-2 in GD follicles and less (P<0.05) activity of IGFBP-3 in GD and GP follicles than other follicles. Activity of IGFBP-4 and -5 was greater (P<0.05) in A and AP follicles than G, GD, and GP follicles. Maintenance of a frequent release of LH pulses over a 16-day period did not result in maintenance of persistent follicles throughout this period indicating that duration of dominance of these follicles is finite even when there is frequent release of LH pulses. Follicular atresia is associated with greater activity of IGFBP-2, -4, -5, and greater concentrations of P4 in follicles, whereas growing dominant and persistent follicles contained greater concentrations of E2, androstenedione (A4), and less IGFBP-2 activity than follicles of other classes. Follicle classifications based on ultrasonography or follicular concentration of steroids did differ (P<0.05) for the largest follicles from the 2PRID group. Two follicles in this group appeared as GD follicles by ultrasonography, but these were atretic based on follicular steroid contents. Objective 1 of the present study yielded the conclusion that concentrations of steroid hormones in follicular fluid and blood plasma could be predictably controlled by regulating the frequency of LH pulses with varying doses of P4. Objective 2 yielded the conclusion that maintain frequent release of LH pulses over a 16-day period could not maintain persistent follicles throughout this period, indicating that duration of dominance of these follicles is finite even when there is frequent release of LH pulses. Follicular atresia in the present study was associated with increased follicular fluid activity of IGFBP-2, -4, -5, and P4, whereas growing dominant and persistent follicles contained greater concentrations of E2, A4, and less IGFBP-2 activity than follicles of other classes.
Domestic Animal Endocrinology | 1986
M. L. Day; K. Imakawa; M. Garcia-Winder; Roger J. Kittok; B.D. Schanbacher; J. E. Kinder
Abstract Secretion of luteinizing hormone (LH) and effects of estradiol were evaluated during and after the prepubertal decline in negative feedback of estradiol on secretion of LH. Prepubertal heifers (269 ± 4 days of age; n=10) were ovariectomized on February 6, 1981 (Day 0). Five ovariectomized heifers were administered a subcutaneous implant on Day 0 which provided physiological serum concentrations of estradiol (OVX-E 2 ). The remaining 5 heifers were not implanted (OVX). A second estradiol implant was administered to OVX-E 2 heifers on Day 164 (n=3) or Day 206 (n=2) of the study. Blood samples were collected sequentially (every 12 min for 8 hr) at approximately two week intervals from Days 0 to 232 of the experiment. The experimental period spanned from approximately 100 days before (269 days of age) to 100 days after (501 days of age) the expected age at puberty. Mean serum concentration of LH and frequency of LH pulses increased rapidly from Days 0 to 36 in OVX heifers and were followed by a further gradual rise in pulse frequency (Day 50 to 232) and a reciprocal decline in mean LH and pulse amplitude. The rapid post-ovariectomy increase in secretion of LH was blocked by estradiol in OVX-E 2 heifers. All characteristics (mean, frequency and amplitude) of secretion of LH increased gradually during the experimental period in OVX-E 2 heifers (Days 0 to 232). Mean concentration and amplitude of pulses were higher in OVX-E 2 than in OVX heifers by Days 148 and 134, respectively. These differences were maintained for the remainder of the experimental period. No acute effects of the second estradiol implant on secretion of LH were observed in OVX-E 2 heifers. Results of this study indicate that long-term changes in secretion of LH occur following prepubertal ovariectomy in heifers and suggest that the previously documented prepubertal decline in negative feedback of estradiol on secretion of LH is followed by a period of positive feedback after pubertal age is surpassed.
Domestic Animal Endocrinology | 1986
M. Garcia-Winder; K. Imakawa; M. L. Day; D. D. Zalesky; Roger J. Kittok; J. E. Kinder
Abstract An experiment was conducted to test if suckling acutely suppressed circulating levels of LH during the postpartum period in beef cows. In addition, the influence of exogenous administration of low concentrations of estradiol on LH secretion during the postpartum period was evaluated. Twelve mature cows were randomly assigned before parturition to one of three treatments. Four intact cows were used as controls (INT). Eight cows were ovariectomized within the first 7 days following parturition. Four of these cows received a silastic 17β-estradiol implant subcutaneously at the time of ovariectomy (OVX-E); the remaining four cows received no further treatment (OVX). All cows were allowed to nurse one calf for 30 min daily between 1200 and 1230 hours for the duration of the experiment. Blood samples were collected at 12 min intervals for 6 hr before and 6 hr after suckling on days 9, 30, 44 and 58 postpartum. Mean interval (mean ± SE) to the first increase in peripheral progesterone concentrations indicative of the onset of ovarian luteal activity was detected in INT cows 37 ± 4.9 days postpartum. An acute effect of suckling on LH secretion did not occur in INT and OVX cows but mean LH concentrations were reduced in OVX-E cows following suckling on days 44 and 58. Mean LH concentrations remained low in INT cows; whereas, in OVX and OVX-E cows LH concentrations increased linearly (P
Domestic Animal Endocrinology | 1991
J. E. Kinder; M. Garcia-Winder; K. Imakawa; M. L. Day; D. D. Zalesky; M.L. D'Occhio; T. T. Stumpf; Roger J. Kittok; B.D. Schanbacher
The objective of the research was to determine the relationship between circulating 17 beta-estradiol (E2) and secretion of luteinizing hormone (LH) in cows. A second objective was to determine if response to E2 was influenced by interval between ovariectomy and the start of E2 treatment. Thirty-one nulliparous cows 3 yr of age were randomly assigned to a 2 x 4 factorial arrangement of treatments. Sixteen cows were ovariectomized at 18 mo of age (long term), and the other 15 cows were ovariectomized at 36 mo of age (short term). At the time of ovariectomy of cows in the short term group, 11 cows in the short term group and 12 cows in the long term group were implanted subcutaneously with 1, 2 or 4 polydimethylsiloxane capsules containing E2. The other eight cows served as non-implanted controls (n = 4-short term, n = 4-long term). All cows were fitted with jugular vein catheters on day 29 of treatment, and on day 30 blood samples were collected at 12-min intervals for 6 hr. At the end of 6 hr, luteinizing hormone-releasing hormone (LHRH) was administered and blood sampling continued at 12-min intervals for an additional hour. Serum was analyzed for LH and E2. Variables of LH secretion analyzed were mean concentration, frequency of pulses, amplitude of pulses and maximum concentration after LHRH. There were no significant interactions for any of the variables of LH among cows ovariectomized for the long and short term. There was a significant linear increase in mean concentration of LH with increased circulating concentration of E2.(ABSTRACT TRUNCATED AT 250 WORDS)
Biology of Reproduction | 1984
M. L. Day; K. Imakawa; M. Garcia-Winder; D. D. Zalesky; B. D. Schanbacher; Roger J. Kittok; J. E. Kinder
Biology of Reproduction | 1994
E. G. M. Bergfeld; F. N. Kojima; Andrea S. Cupp; M. E. Wehrman; K. E. Peters; M. Garcia-Winder; J. E. Kinder
Journal of Animal Science | 1986
K. Imakawa; M. L. Day; M. Garcia-Winder; D. D. Zalesky; Roger J. Kittok; B. D. Schanbacher; J. E. Kinder
Journal of Animal Science | 1986
K. Imakawa; M. L. Day; D. D. Zalesky; M. Garcia-Winder; Roger J. Kittok; J. E. Kinder
Biology of Reproduction | 1984
M. Garcia-Winder; K. Imakawa; M. L. Day; D. D. Zalesky; Roger J. Kittok; J. E. Kinder