JDR JDR Most Read Articles
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Full Text
Right arrow Full Text (PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via ISI Web of Science (8)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Graves, D.T.
Right arrow Articles by Krall, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Graves, D.T.
Right arrow Articles by Krall, E.

Inflammation is More Persistent in Type 1 Diabetic Mice

D.T. Graves*, G. Naguib, H. Lu, C. Leone, H. Hsue, and E. Krall

Department of Periodontology and Oral Biology, Boston University School of Dental Medicine, Suite W-202D, 700 Albany Street, Boston, MA 02118, USA;



View larger version (12K):

[in a new window]
 
Figure 1. P. gingivalis stimulates formation of a more persistent inflammatory infiltrate in diabetic mice. Diabetes was induced by multiple low-dose streptozotocin treatment, while control mice were treated with citrate buffer alone. (A) P. gingivalis (5 x 108) or (B) P. gingivalis (1 x 108) was inoculated s.c. into the scalp. The degree of PMN infiltration was measured in H&E-stained sections at the center of the infiltrate. A scale was used ranging from no inflammation to severe inflammation with necrosis (0–9). Results are shown as mean ± SEM of 6 mice per group. *A significant difference (P < 0.05) between the control and diabetic groups.

 


View larger version (16K):

[in a new window]
 
Figure 2. Diabetes causes prolonged expression of MIP-2 in response to P. gingivalis. Diabetes was induced and P. gingivalis was inoculated into the scalp as described in Fig. 1Go. RNA was extracted from the soft tissue and analyzed by RPA. The density of each band was quantified and normalized according to the level of GAPDH expression in the same lane. Each value represents the mean of 3 different RPAs ± standard deviation. (A) P. gingivalis (5 x 108); (B) P. gingivalis (1 x 108). *A significant difference (P < 0.05) between the control and diabetic groups.

 


View larger version (14K):

[in a new window]
 
Figure 3. Diabetes causes prolonged expression of MCP-1 in response to P. gingivalis. Diabetes was induced and P. gingivalis was inoculated into the scalp as described in Fig. 1Go. RNA was extracted from the soft tissue and analyzed by RPA. The density of each band was quantified and normalized according to the level of GAPDH expression in the same lane. Each value represents the mean of 3 different RPAs ± standard deviation. (A) P. gingivalis (5 x 108); (B) P. gingivalis (1 x 108). *A significant difference (P < 0.05) between the control and diabetic groups.

 





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
IADR Journals Advances in Dental Research ®
Journal of Dental Research ® Critical Reviews (1990-2004)
Copyright © 2005 Institutional Access Guidelines