Bryan K A, Hammond J M, Canning S, Mondschein J, Carbaugh D E, Clark A M, Hagen D R
Dept. of Dairy and Anim. Sci., Pennsylvania State University, University Park 16802.
J Anim Sci. 1989 Jan;67(1):196-205. doi: 10.2527/jas1989.671196x.
Forty gilts (mean wt = 72 kg) were administered daily either vehicle (C = control) or 70 micrograms porcine growth hormone (pGH)/kg BW. After 30 d of treatment, eight gilts per group (Exp. 1) were slaughtered and blood, uteri and ovaries were collected. Follicular fluid (FFl) was collected and granulosa cells (GC) were cultured. The remaining gilts (Exp. 2) were treated for up to 35 additional days and examined twice daily for estrus. Estrusal gilts were removed from the experiment. Noncyclic gilts (n = 9 of 12 pGH; n = 4 of 12 C) were slaughtered on d 66 and their ovaries were examined. Ovarian weights were not different for pGH and C gilts in either Exp. 1 (P greater than .1) or Exp. 2 (P = .09). Uterine weights were greater for pGH-treated than for C gilts (P less than .007) in Exp. 1, but not in Exp. 2. Concentrations of estradiol (E2) in plasma and FF1 and of progesterone (P) in plasma and FF1 were not different for pGH and C gilts. Concentrations of insulin-like growth factor-I (IGF-I) in FF1 and in serum were greater for pGH than for C gilts (P less than .01). Concentration of P in serum-free medium of cultured GC was lower for GH than for C (P less than .05) in the presence or absence of gonadotropins in Exp. 1. The FSH-stimulated secretion of P was also lower for GC of pGH-treated gilts in Exp. 2, indicating a failure of GC to differentiate in culture. Only one pGH gilts in Exp. 2 manifested estrus, compared with seven C gilts (P less than .025). In Exp. 1, ADG was higher (P less than .03) and feed/gain lower (P less than .07) for pGH gilts. Longissimus muscle area (LMA) was not different (P = .19) between groups. Backfat thickness (BF) was lower (P less than .005) in pGH than in C in both Exp. 1 and 2. We conclude that exogenous pGH increased growth rate, improved feed efficiency and altered carcass traits in gilts. However, these effects were associated with impaired ovarian development of prepubertal gilts and a low incidence of estrus.
40头后备母猪(平均体重 = 72千克)每天分别注射赋形剂(C = 对照组)或70微克/千克体重的猪生长激素(pGH)。治疗30天后,每组8头后备母猪(实验1)被屠宰,采集血液、子宫和卵巢。收集卵泡液(FFl)并培养颗粒细胞(GC)。其余后备母猪(实验2)再额外治疗35天,并每天检查两次发情情况。出现发情的后备母猪被排除在实验之外。未出现发情周期的后备母猪(pGH组12头中有9头;C组12头中有4头)在第66天被屠宰并检查其卵巢。在实验1(P>0.1)或实验2(P = 0.09)中,pGH组和C组后备母猪的卵巢重量没有差异。在实验1中,pGH处理的后备母猪子宫重量大于C组(P<0.007),但在实验2中并非如此。pGH组和C组后备母猪血浆和FF1中的雌二醇(E2)浓度以及血浆和FF1中的孕酮(P)浓度没有差异。pGH组FF1和血清中的胰岛素样生长因子-I(IGF-I)浓度高于C组(P<0.01)。在实验1中,无论有无促性腺激素,GH处理的GC在无血清培养基中的P浓度均低于C组(P<0.05)。在实验2中,pGH处理的后备母猪的GC经促卵泡素刺激后的P分泌也较低,表明GC在培养中未能分化。在实验2中,只有1头pGH组后备母猪出现发情,而C组有7头(P<0.025)。在实验1中,pGH组后备母猪的平均日增重较高(P<0.03),料重比更低(P<0.07)。两组之间的背最长肌面积(LMA)没有差异(P = 0.19)。在实验1和实验2中,pGH组的背膘厚度(BF)均低于C组(P<0.005)。我们得出结论,外源性pGH提高了后备母猪的生长速度,改善了饲料效率并改变了胴体性状。然而,这些影响与青春期前后备母猪卵巢发育受损以及发情发生率低有关。