Stereological sex difference during development of the magnocelluar subdivision of the medial preoptic nucleus (MPN mag).

In Syrian hamsters, reproductive behaviors are initiated in the presence of appropriate hormonal and chemosensory cues. These cues are detected and integrated within a highly conserved pathway that converges on a small nuclear group in the lateral aspect of the medial preoptic area, the magnocellular subdivision of the medial preoptic nucleus (MPN mag). The MPN mag plays a critical role in the regulation of male mating behavior--bilateral ablation of the MPN mag eliminates copulation. The MPN mag is sexually differentiated in both neuron number and density, but not in overall volume or volume of individual neurons. The current study used unbiased stereological methods to determine when the MPN mag becomes sexually differentiated. Our data indicate that the MPN mag becomes sexually dimorphic in volume and cell number after the critical period when steroid treatment induces male sexual behavior.

Sex differences in the magnocellular subdivision of the medial preoptic nucleus in Syrian hamsters.

Exposure to pheromonal cues initiates male mating behavior. Pheromones are processed within a pathway that converges on the magnocellular subdivision of the medial preoptic nucleus. Lesions of this area eliminate male copulatory behavior, but do not affect anogenital investigation. Exposure to pheromones stimulates cells of the magnocellular subdivision of the medial preoptic nucleus in a sex-specific manner. In this study, we hypothesize that sex differences in cell number may underlie sex differences in pheromone-induced neural stimulation. The current study used unbiased stereological methods to identify sexual dimorphisms in the magnocellular subdivision of the medial preoptic nucleus. Sex differences were found in the number and density of neurons, but not in overall volume or neuron volume. Consequently, the total volume is not sexually differentiated because neurons are more densely packed within the male magnocellular subdivision of the medial preoptic nucleus. These results support the hypothesis that additional neurons in the magnocellular subdivision of the medial preoptic nucleus are critical for the expression of male copulatory behaviors in adulthood. Furthermore, they suggest that sexual differentiation of the magnocellular subdivision of the medial preoptic nucleus is an important process that forms the anatomical basis for sex-specific behavioral responses to pheromonal stimulation.

Reduced glucose-induced neuronal activation in the hypothalamus of diet-induced obese rats.

Rats predisposed to develop diet-induced obesity (DIO) preferentially activate their sympathetic nervous system during intracarotid glucose infusion [B.E. Levin, Intracarotid glucose-induced norepinephrine response and the development of diet-induced obesity, Int. J. Obesity 16 (1992) 451-457.] but their brains are generally less responsive to glucose than diet-resistant rats (DR) [B.E. Levin, K.L. Brown, A.A. Dunn-Meynell, Differential effects of diet and obesity on high and low affinity sulfonylurea binding sites in the rat brain, Brain Res. 739 (1996) 293-300.; B.E. Levin, B. Planas, Defective glucoregulation of brain alpha2-adrenoceptors in obesity-prone rats, Am. J. Physiol. 264 (1993) R305-R311.; B.E. Levin, A.C. Sullivan, Glucose-induced norepinephrine levels and obesity resistance, Am. J. Physiol. 253 (1987) R475-R481.; B.E. Levin, A.C. Sullivan, Glucose-induced sympathetic activation in obesity-prone and resistant rats, Int. J. Obesity 13 (1989) 235-246.]. Here, 1 h intracarotid glucose infusions (4 mg/kg/min) selectively increased Fos-like immunoreactivity (FLIR) in the hypothalamic paraventricular, ventromedial, dorsomedial and arcuate nuclei of inbred DR but not DIO rats. This suggests that enhanced glucose-induced sympathetic activation in DIO rats is related to a failure of glucose to produce neuronal activation in these areas.