Abstract

The current study evaluated the effect of glutamate supply on the onset of puberty and possible links to changes in serum concentrations of insulin [INS], glucose [GLU] and triiodothyronine [T 3]. The study was conducted from June to November in prepuberal female goats ( n = 18; 3 mo. old, 7/8 Saanen-Alpine, 1/8 Criollo, 26° north) randomly assigned to two experimental groups: (i) excitatory amino acids group (group AA, n = 10; 16.52 ± 1.04 kg LW, 3.4 ± 0.12 body condition score [BCS], receiving an intravenous infusion of 7 mg kg −1 live weight [LW] of l-glutamate, twice a week, and (ii) control group (group CC, n = 8; 16.1 ± 1.04 kg LW, 3.1 ± 0.12 BCS) receiving saline. Blood samples were obtained twice a week, for assessing progesterone [P 4], as well as in a monthly basis to evaluate INS and T 3 by RIA. Mean final LW and BCS were 23.2 ± 0.72 kg, 3.53 ± 0.10 units, without differences between groups. The AA group depicted an earlier onset of puberty (6.9 ± 0.3 compared to 7.5 ± 0.4 mo.; P < 0.05) and an increased ovarian activity (70 ± 0.28% compared to 25 ± 0.26%; P < 0.05). Neither serum INS concentrations nor serum glucose concentrations differed between treatments (1.2 ± 0.06 ng mL −1 and 89.6 ± 1.8 mg 100 mL −1; P > 0.05, respectively). Serum T 3 concentrations, however, were greater in AA goats (1.55 ± 0.03 compared to 1.39 ± 0.04 ng mL −1). In addition, a treatment x time interaction occurred ( P < 0.05) across the experimental period for both T 3 and INS, with increases by the last third of the experimental period, time at which the onset of puberty occurred in both experimental groups. No differences ( P > 0.05) for glucose concentrations across time occurred between treatments. Results indicate that, in prepuberal goats, glutamate acts as a cue for sexual maturation in a glucose-independent pathway, while both T 3 and INS seem to act as metabolic modulators for the establishment of puberty in goats. Actions of INS and T 3 are mediated directly on hypothalamic centers regulating the pulsatile release of GnRH or indirectly by peripheral cues reflecting INS-T 3 actions on somatic development remains to be determined.

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