In the rat median eminence immunoreactive galanin nerve fibers and terminals are present in high numbers in the external layer, and fibers in moderate numbers are seen in the internal layer. The possible sources of these galanin-containing fibers were studied by means of radioimmunoassay and immunohistochemistry in rats with different types of hypothalamic lesions. Galanin-like neurons were found both (1) in the magnocellular hypothalamo-neurohypophyseal system and (2) in the parvocellular hypothalamo-median eminence-anterior pituitary system. Cell bodies containing galanin-like immunoreactivity were localized in the supraoptic, magnocellular paraventricular and accessory magnocellular neurons with axons traversing the internal layer and terminating in the posterior pituitary. Surgical isolation of these neurons from the median eminence resulted in a marked depletion of immunoreactive galanin from the internal layer of the median eminence and the posterior pituitary. Due to the retrograde accumulation of axonally transported substances in cells proximal to the lesions, immunoreactive galanin-like cells became visible in the supraoptic and paraventricular nuclei ipsilateral to the knife cuts, and levels of galanin-like immunoreactivity increased in these nuclei 7 days after bilateral transections of the hypothalamo-hypophyseal tract. Immunoreactive galanin fibers in the external layer of the median eminence around the portal capillaries were found to be of paraventricular and arcuate nucleus origin. Bilateral paraventricular lesions caused marked (70%) reduction in levels of galanin-like immunoreactivity in the median eminence. The remaining 30% of the galanin immunoreactivity in the external layer may arise from the arcuate nucleus, which contains a great number of galanin-containing cell bodies. Thus, galanin-like immunoreactivity accumulated retrogradely in parvocellular paraventricular and arcuate nucleus neurons after transections of their fibers in the lateral retrochiasmatic area or in the median eminence, respectively.

This content is only available via PDF.
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
You do not currently have access to this content.