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Endocrinology Vol. 147, No. 10 4843-4851
Copyright © 2006 by The Endocrine Society

Morphological Plasticity in the Neural Circuitry Responsible for Seasonal Breeding in the Ewe

Van L. Adams, Robert L. Goodman, A. K. Salm, Lique M. Coolen, Fred J. Karsch and Michael N. Lehman

Departments of Physiology and Pharmacology (V.L.A., R.L.G.) and Neurobiology and Anatomy (A.K.S.), West Virginia University Health Sciences Center, Morgantown, West Virginia 26506; Reproductive Sciences Program (F.J.K.), Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor Michigan 48109; and Department of Anatomy and Cell Biology (L.M.C., M.N.L.), University of Western Ontario, London, Ontario N6A 5C1, Canada

Address all correspondence and requests for reprints to: Dr. Robert L. Goodman, Department of Physiology and Pharmacology, PO Box 9229, West Virginia University, Morgantown, West Virginia. E-mail: bgoodman{at}hsc.wvu.edu.

An increase in the response of GnRH neurons to estrogen negative feedback is responsible for seasonal anestrus in the ewe, but the underlying neural mechanisms remain largely unknown. Neural plasticity may play an important role because the density of synaptic input to GnRH neurons changes with seasons. Moreover, the transition from breeding to anestrous season requires thyroid hormones, which are also required for neuronal development. In the first experiment, we examined whether the decrease in synapses on GnRH neurons is critical for the transition to anestrus by comparing synaptic input in thyroidectomized and thyroid-intact controls, using electron microscopic analysis. Thyroidectomized ewes remained in the breeding season, but the number of synaptic contacts on their GnRH cells was not different from those in thyroid-intact ewes that were anestrus. The next experiment tested whether there was a seasonal change in morphology of the A15 dopaminergic neurons that mediate estrogen negative feedback during anestrus by analyzing synapsin-positive close contacts onto A15 neurons with confocal microscopy. There was a 2-fold increase in these close contacts onto dendrites of A15 neurons in anestrus and a corresponding increase in the length of A15 dendrites at this time of year. The increase in dendritic length was blocked by thyroidectomy, but this procedure did not significantly affect synaptic input to A15 neurons. These results provide initial evidence that the seasonal change in synapses on GnRH neurons is not sufficient for the transition into anestrus but that plasticity of the A15 dopaminergic neurons mediating estrogen negative feedback may contribute to this seasonal alteration.




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