4.6 Article

Pulpal Response to the Combined Use of Mineral Trioxide Aggregate and Iloprost for Direct Pulp Capping

Journal

APPLIED SCIENCES-BASEL
Volume 11, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/app11083702

Keywords

iloprost; inflammation; mineralization; pulp capping material; mineral trioxide aggregate; rat dental pulp

Funding

  1. Research Initiative from the Prince Naif bin Abdulaziz Health Research Center, King Saud University Medical City, Riyadh, Saudi Arabia

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The study evaluated the effects of using iloprost, MTA, and MTA-iloprost as pulp capping materials on pulpal inflammation and tertiary dentin formation in rat molars. Results showed similar pulpal responses in all groups, suggesting that mixing MTA with iloprost might not have significant clinical benefits.
Purpose: The present study aims to assess the combined effects of mineral trioxide aggregate (MTA) and iloprost when used as a pulp capping material on pulpal inflammation and tertiary dentin formation compared with MTA and iloprost alone in rat molar teeth. Methods: Eighty maxillary first molar rat teeth were exposed and capped with iloprost solution, MTA, or MTA mixed with iloprost (MTA-iloprost). The cavities were then filled with resin-modified glass ionomer. The cavity was restored with glass ionomer without the use of pulp capping agent in the control group. The rats were sacrificed after one and four weeks. Block sections of the molar specimens were prepared and subjected to hematoxylin and eosin staining for evaluation. Statistical analysis was done using the Kruskal-Wallis test, followed by Dunnett's test. Results: At week one, the control group showed significantly more severe pulpal inflammatory reactions than the iloprost (p = 0.00), MTA (p = 0.04), and MTA-iloprost (p = 0.00) groups. Hard tissue formation was commonly found in the iloprost, MTA, and MTA-iloprost groups. After four weeks, pulpal tissue degeneration was observed in the control group. Complete hard tissue barriers were found in 50%, 72.7%, and 77.8% of the specimens in iloprost, MTA, and MTA-iloprost groups, respectively, with no significant differences among the experimental groups. The dentinal tubule patterns were mostly regular in the MTA-iloprost group and irregular in the iloprost and MTA groups. Conclusions: The application of iloprost, MTA, and MTA-iloprost as a pulp capping material resulted in similar pulpal responses in the mechanically exposed pulp of rat molars. Therefore, mixing MTA with iloprost might not be clinically significant.

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