Restoration of the luteinizing hormone surge in middle-aged female rats by altering the balance of GABA and glutamate transmission in the medial preoptic area

Abstract

Hypothalamic glutamate and gamma-aminobutyric acid (GABA) neurotransmission are involved in the ovarian hormone-induced GnRH-LH surge in rodents. We previously reported that middle-aged rats have significantly less glutamate release in the medial preoptic area than young rats on the day of the LH surge. The present study tested the hypothesis that the delayed and attenuated LH surge in ovariohysterectomized middle-aged rats primed with ovarian steroids results from reduced hypothalamic glutamate and increased GABA(A) neurotransmission. Microdialysis results show that middle-aged rats with attenuated LH surges had reduced extracellular glutamate and increased extracellular GABA levels in the medial preoptic area compared with young rats. Blocking GABA(A) receptors with bicuculline or inhibiting synaptic glutamate reuptake with L-trans-pyrrolidine-2,4-dicarboxylic acid increased extracellular Glu in the medial preoptic area and partially restored LH surge amplitude in middle-aged rats without altering LH surge onset. Complete recovery of LH surge amplitude was observed in middle-aged rats treated with the combination of bicuculline and L-trans-pyrrolidine-2,4-dicarboxylic acid. This treatment also restored the extracellular glutamate:GABA ratio in the medial preoptic area of middle-aged rats to the level of young rats. Immunoblot analysis revealed that estradiol and progesterone treatment reduced SLC32A1(formerly known as vesicular GABA transporter) levels and increased SLC17A6 (formerly known as vesicular glutamate transporter 2) levels in the anterior hypothalamus of ovariohysterectomized young but not middle-aged rats. These data suggest that both reduced availability of glutamate and increased activation of GABA(A) receptors under estrogen-positive feedback conditions contribute to the age-related delay in onset and attenuated amplitude of the LH surge.

Figure 1

(A) Illustration of microdialysis probes placements in the medial preoptic area. The diagram corresponds to a coronal section at approximately 0.0 mm relative to Bregma according to the atlas of Paxinos and Watson [81]. Medial preoptic area (MPA); third ventricle (3V); och (optic chiasm); ventromedial preoptic nucleus (VMPO), ventrolateral preoptic nucleus (VLPO); anteroventral periventricular nucleus (AVPe); supraoptic nucleus (SO); Alar nucleus(Al); Strial part preoptic nucleus (StA); (●) young rats; (■) middle-aged rats. (B) Photomicrograph of thionin-stained coronal section, magnification 4x, showing the approximate location of a microdialysis probe. The arrow indicates the site of probe placement.

Figure 2

Middle-aged (M) rats exhibit a delayed and attenuated GnRH-LH surge that is accompanied by decreased extracellular Glu and increased extracellular GABA in the mPOA on the day of the GnRH-LH surge relative to young (Y) rats. Data are from GnRH-LH surges generated in Y (n=8) and M (n=7) rats primed with E2B and P as described in Methods. Time 0 represents the time of the P injection at 0900 h. (A) LH, (B) extracellular Glu (C) extracellular GABA levels in the mPOA. * P<0.001. See Table 1 for additional quantitation and statistical comparisons.

Figure 3

Elevation of extracellular Glu and inhibition of extracellular GABA in the mPOA can increase GnRH-LH surge amplitude in middle-aged females. Data are means ± SEM of Y (N=7) controls, M (N=6) controls, MS (middle-aged controls with saline infusion at 0900 and 1300 hr; N=5), M infused at 0900 and 1300 hr with 10 μM bicuculline (M+B, N=5), M reverse dialyzed with 10 mM TPDC (M+T, N=6) and M treated with a combination of 10 μM bicuculline and 10 mM TPDC (B+T, N=6). Time 0 is relative to the P injection at 0900 h. Each treatment is illustrated on separate panels with the appropriate middle-aged control group graphed for comparison. The same young control (Y) is depicted in each panel. See Figure 4 and Table 2 for additional quantitation and statistical comparisons.

Figure 4

Increasing mPOA Glu release and decreasing mPOA GABA_A receptor activation with TPDC plus bicuculline rescues total LH release. Because M and MS were not significantly different, data from M are illustrated. Total LH (A), Glu (B), GABA (C) and Glu:GABA ratio (D) during the GnRH-LH surge in Y ( N=8), M (N=6), M+B (N=5), M+T (N=6) and M+B+T (N=6) rats are illustrated. *Significantly different than Y (P<0.01). **Significantly different than M (P<0.05).

Figure 5

Effects of steroid priming on VGAT and VGLUT2 abundance in the anterior and posterior hypothalamus. Representative Western blot gels showing abundance of synaptosomal VGAT and VGLUT2 in hypothalamic regions from vehicle and E2B + P-treated young and middle-aged rats are illustrated (A). SYP (formerly known as synaptophysin) was used as a marker for synaptosomes. ACTB (formerly known as β-actin), a cytoskeletal protein, was used as a loading control. The VGLUT2 and VGAT band densities were normalized to the SYP band density in the same sample. Normalized band density of young (Y), vehicle-treated rats (control) was assigned a value of 1 for comparison with all other groups (B-G). All values are mean ± SEM of 5-6 independent replications (*, P<0.05 versus young vehicle; **, P<0.05 versus young E2B + P).