Groups of Wistar rats and albino hamsters were given six different experimental diets containing 56% of either glucose, sucrose, amylopectin or combinations of glucose and amylopectin. Half of the animals were infected with a mixture of four strains of Streptococcus mutans. The rats were kept in an automatic feeding machine whereas the hamsters were caged in ordinary macrolon cages. Caries was scored after 80 days. Animals infected with S. mutans developed more caries in all dietary groups than noninfected. All types of caries, buccolingual, sulcal and proximal, were increased. Especially in the sucrose group, both in rats and hamsters, a pronounced occurrence of smooth surface caries was found, infected animals having 4–15 times as many smooth surface caries lesions as noninfected ones. Thus, the combination S. mutans-sucrose showed an outstanding picture of rampant caries in comparison to all other groups. Amylopectin could not substitute for extracellular glucan formation by S. mutans either alone or in combination with glucose.

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.