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and androgen receptor mRNA levels in feedlot steers



* Animal Growth and Development Laboratory, Department of Animal Science, University of Minnesota, 348 ABLMS, Eckles Avenue, St. Paul, MN 55108, USA
Department of Animal Sciences & Industry, Kansas State University, Manhattan, KS 66506, USA
Abstract
We have previously shown that a combined trenbolone acetate (TBA)/ estradiol-17β (E2) implant significantly increases IGF-I mRNA levels in LM of feedlot steers by 28 d after implantation. Here we compare the effects of E2 (25.7 mg), TBA (120 mg) and combined TBA (120 mg)/ E2 (24 mg) implants on IGF-I, IGF-I receptor (IGFR-1), estrogen receptor (ER)-
and androgen receptor (AR) mRNA levels in the LM of steers implanted for 28 d. Five yearling steers per group were implanted with each implant and 5 control steers received no implant. Steers were weighed weekly starting on d 0 and muscle biopsy samples were taken from each steer on d 0 (before implantation), d 7, d 14 and d 28. RNA was prepared from each sample and real-time RT-PCR was used to determine the levels of IGF-I, IGFR-1, ER-
and AR mRNA. Body weight of implanted steers, adjusted using d 0 BW as a covariant, tended (P = 0.09) to be greater than that of control steers. On d 7 and 28 IGF-I mRNA levels were greater (58% and 78%, respectively; P < 0.009) in E2 implanted animals than in control steers. Similarly, on d 28 the LM IGF-I mRNA level was 65% greater (P = 0.017) in TBA/E2 implanted steers than in control animals. In contrast, the TBA implant did not increase (P = 0.99) LM IGF-I mRNA levels after 28 d of implantation. Muscle IGFR-1, AR and ER-
mRNA level were not different (P > 0.47) in any of the treated groups compared with the control group. These data suggest that E2 is responsible for the increased muscle IGF-I mRNA level observed in steers implanted with a combined TBA/E2 implant.
Key Words: bovine estradiol-17β IGF-I muscle trenbolone acetate
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