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[Abstract Title]. - Society for Neuroscience

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Poster<br />

279. Steroids and Plasticity I<br />

Time: Sunday, November 16, 2008, 1:00 pm - 5:00 pm<br />

Program#/Poster#: 279.9/MM23<br />

Topic: E.01.c. Steroids and plasticity<br />

Support: NIH Grant DA08259<br />

NIH-MSTP Grant GM07739<br />

<strong>Title</strong>: Sex differences in the level and subcellular distribution of delta-opioid receptor<br />

immunoreactivity in hippocampal principal cells<br />

Authors: *T. J. WILLIAMS 1,2 , A. TORRES-REVERON 1 , T. A. MILNER 1,3 ;<br />

1 Neurol and Neurosci, Weill Cornell Med. Coll, New York, NY; 2 Weill<br />

Cornell/Rockefeller/Sloan-Kettering Tri-Institutional MD-PhD Program, New York, NY; 3 Lab.<br />

of Neuroendocrinology, The Rockefeller Univ., New York, NY<br />

<strong>Abstract</strong>: Our previous studies revealed that ovarian steroids influence endogenous opioid<br />

peptide levels and trafficking of mu-opioid receptors (MORs) in the rat hippocampal <strong>for</strong>mation<br />

(HF). However, whether ovarian steroids affect the levels or trafficking of delta opioid receptors<br />

(DORs) in the HF is unknown. Here, the brains of proestrus (as assessed by vaginal smear<br />

cytology) female, diestrus female, and male adult (2-3 month old) Sprague-Dawley rats were<br />

perfusion fixed with para<strong>for</strong>maldehyde and acrolein. Vibratome cut coronal sections through the<br />

HF were processed <strong>for</strong> quantitative immuno-peroxidase light microscopy or immuno-gold<br />

electron microscopy using antisera directed against the DOR (Chemicon, rabbit polyclonal;<br />

Cheng et al., 1995, guinea pig polyclonal). Consistent with previous studies in males (Commons<br />

and Milner 1996, 1997), DOR-immunoreactivity (-ir) localized to select interneurons and<br />

principal cells in the female HF. Light microscopic densitometry analysis, per<strong>for</strong>med by<br />

hippocampal region using NIH Image, revealed that in comparison to males, proestrus (high<br />

estrogen) females display reduced DOR-ir in the CA1 pyramidal cell layer while diestrus<br />

females show reduced DOR-ir in the dentate granule cell layer. No differences were observed<br />

between males and females within CA1 or dentate hilar interneurons. Electron microscopic<br />

analysis showed reduced total DOR labeling per dendrite and reduced localization of DORs to<br />

the dendritic plasmalemma within CA1 stratum radiatum in females (regardless of estrous phase)<br />

compared to males. Further analysis suggested that diestrus females had reduced total DOR per<br />

dendrite while proestrus females exhibited decreased plasmalemmal distribution of DORs.<br />

Postsynaptic DOR activation is thought to increase potassium conductance and hyperpolarize<br />

membranes. Thus, proestrus females, with fewer plasmalemmal DORs available <strong>for</strong> ligand

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