The norepinephrine content of hypothalamus in vehicle-treated control rats gradually increases between days 16 and 45 of life. Norepinephrine contents of the hypothalamus and mesencephalon of the thyroxine-treated (10 µg/g b.w., s.c., days 8–10) animals also increase between days 16 and 21. Mesencephalic and hypothalamic dopamine contents show no definite patterns throughout this period. The norepinephrine content of both regions is higher in the thyroxine-treated than in control animals between days 16 and 21. Hypothalamic dopamine content is higher and mesencephalic dopamine is lower in thyroxine-treated than in control animals between days 16–21. Corticosterone treatment (20 µg/g b.w., i.p., days 2–4) results in lower norepinephrine content of both regions, lower dopamine content of hypothalamus and higher dopamine content of mesencephalon between days 16 and 21. Thyroxine treatment (days 8–10) counteracts all these effects of the corticosteroid in animals receiving both treatments. Thus, neonatal thyroxine and/or corticosterone treatment significantly affect the developmental pattern of hypothalamic and mesencephalic catecholamines.

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.