Distribution and repeatability of anterior pituitary responses to GnRH and relationship of response classification to the postpartum anovulatory interval of beef cows

Our objectives were to investigate the phenotypic variation in anterior pituitary responsiveness to GnRH (100 mu g, i.v.) of beef cows between d 5 and 8 postpartum, estimate repeatability, and determine the relationship between response classification and duration of the postpartum anovulatory interval (PPI). Brahman x Hereford (F-1) cows (n = 137) and primiparous heifers(n = 58) were evaluated. Response classifications (Class) included peak LH (Low, Intermediate, or High; Class I) and time to peak LH (Early, 10 to 30 min or Late, 60 to 120 min; Class II). The independent effects of Class I and II on PPI were determined in 145 of 195 cows through twice-weekly serum samples analyzed for progesterone. For Class I, pituitary responses to GnRH approximated a normal distribution and, by definition, differed (P < .001) in magnitudes of peak. LH and area under the curve (AUC). For Class II, 111 and 84 cows exhibited early and late peaks, respectively; mean AUC was greater (P < .05) in cows exhibiting late compared with early peaks. Pretreatment LH (P < .01) and estradiol-17 beta (P < .004) influenced responses in one or both response classes. Pluriparous cows had shorter (P < .035) PPI than primiparous cows. Class I did not influence the duration of the PPI; however, in Class II, cows with late peaks exhibited an average PPI that was 8 d shorter (P < .025) than in those with an early peak. To estimate repeatability of pituitary responses, 18 classified cows were subsequently rechallenged with GnRH at d 170 of gestation and at the next postpartum period. Although means for each of these challenges differed (P < .05) throughout in both Classes I and II, the small sample size used to make the estimate failed to yield significant (P > .10) interclass correlations. Nevertheless, overall results provide evidence that variability in individual pituitary responses to GnRH could be targeted as a selection marker to improve reproduction.