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Regenerative Effects of Scrophularia Striata and Adipose Tissue–Derived Stem Cells on Dental Pulp Tissue: An Animal Model

Document Type : Original Article

Authors
1 Research Center for Prevention of Oral and Dental Diseases, Baqiyatallah University of Medical Sciences, Tehran, Iran Department of Endodontics, School of Dentistry, Baqiyatallah University of Medical Sciences, Tehran, Iran
2 Dental Research Center, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran
3 Tissue Engineering and Regenerative Medicine Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
4 Chemical Injuries Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran
5 Department of Physiology and Medical Physics, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran
10.30491/tm.2026.571330.1919
Abstract
Introduction: This study aimed to determine the effects of Scrophularia striata and adipose tissue–derived stem cells on the expression of Kruppel-like factor 4 (KLF4), monocyte chemoattractant protein-1, and brain-derived neurotrophic factor genes during pulp tissue regeneration.
Methods: The methanolic extract of Scrophularia striata was prepared by maceration (Scro). Adipose tissue was harvested from the bilateral inguinal region of rats that did not undergo surgery, and adipose-derived stem cells (SC) were isolated and characterized. Pulp inflammation was induced in the rats, and pulpectomy was performed at the end of the second week. After placement of a triple-antibiotic paste for 2 weeks, regenerative treatment with drugs and materials was performed. The teeth were randomly divided into four groups (n = 4/group): (1) control (blood clot only), (2) Scrophularia alone (Scro), (3) stem cells alone (SC), and (4) Scrophularia + stem cells (SC+Scro). One to four weeks after tooth filling, the dental pulp was harvested from the animals. Real-time PCR was used to measure the expression levels of KLF4, MCP-1, and BDNF genes.
Results: The highest level of KLF4 expression was observed in the SC group (P = 0.001), which was significantly reduced in the SC+Scro group compared with the SC group (P = 0.001). Injection of Scro significantly decreased MCP-1 gene expression compared with the control group (P = 0.001). Injection of Scro, SC, and SC+Scro significantly increased BDNF gene expression compared with the control group (P = 0.001). The highest BDNF expression was observed in the Scro group (P = 0.001), which was significantly reduced in the SC+Scro group compared with the Scro and SC groups (P = 0.001).
Conclusion: Application of the Scro extract increased the expression of KLF4 and BDNF genes and decreased MCP-1 expression. Application of the Scro+SC combination increased the expression of KLF4, BDNF, and MCP-1 genes.
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Articles in Press, Accepted Manuscript
Available Online from 15 February 2026

  • Receive Date 07 January 2026
  • Accept Date 01 February 2026