Mehrdad Moetamani-Ahmadi, Seyedeh Elnaz Nazari, Fereshteh Asgharzadeh, Nima Zafari, Mahla Velayati, Hamed Akbarzade, Maryam Alaei, Zhara Negahbanzaferanloo, Elmira Lagzian, Ibrahim Saeed Gataa, Seyed Mahdi Hassanian, Gordon A Ferns, Majid Khazaei, Amir Avan
{"title":"加厚石榴对大鼠子宫角粘连模型术后粘连形成的抑制作用。","authors":"Mehrdad Moetamani-Ahmadi, Seyedeh Elnaz Nazari, Fereshteh Asgharzadeh, Nima Zafari, Mahla Velayati, Hamed Akbarzade, Maryam Alaei, Zhara Negahbanzaferanloo, Elmira Lagzian, Ibrahim Saeed Gataa, Seyed Mahdi Hassanian, Gordon A Ferns, Majid Khazaei, Amir Avan","doi":"10.2174/0113816128337474250311074502","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Despite recent advances in surgical procedures, postoperative peritoneal adhesions are common following major abdominopelvic surgery. Here, the therapeutic potential of Punica granatum var. pleniflora (PGP) on postoperative peritoneal adhesions has been explored in a rat uterine horn adhesion model.</p><p><strong>Method: </strong>Eighteen Albino Wistar female rats were divided into three groups: control group, sham, and treatment group receiving 400 mg/kg/day PGP orally for ten days. An identical surgical technique was employed to induce adhesion of the uterine horn in both the control and treatment groups. At the end of the experiments, all rats were re-operated for evaluation of adhesion. The macroscopic evaluation and fibrotic bands scaling were conducted and inflammation and fibrosis were assessed and graded, microscopically. Additionally, the effect of PGP on inflammation and fibrosis was assessed via PCR, ELISA, and histopathology.</p><p><strong>Results: </strong>PGP could significantly reduce the peritoneal adhesion score (treatment group vs. control group; P<0.001). Histopathological analysis indicated that PGP prevented adhesion formation by suppressing inflammation and fibrosis. Moreover, inflammatory and fibrosis biomarkers were decreased following PGP treatment. Furthermore, rats in the treatment group had significantly lower oxidative stress markers in adhesion tissues when compared to the control group.</p><p><strong>Conclusion: </strong>Oral PGP was associated with reduced peritoneal adhesion formation in rats, postoperatively. This therapy might be an effective and safe strategy for preventing intraperitoneal adhesion after abdominopelvic surgeries.</p>","PeriodicalId":10845,"journal":{"name":"Current pharmaceutical design","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Treatment with Punica granatum var. pleniflora Inhibits Postoperative Adhesion Formation in a Rat Uterine Horn Adhesion Model.\",\"authors\":\"Mehrdad Moetamani-Ahmadi, Seyedeh Elnaz Nazari, Fereshteh Asgharzadeh, Nima Zafari, Mahla Velayati, Hamed Akbarzade, Maryam Alaei, Zhara Negahbanzaferanloo, Elmira Lagzian, Ibrahim Saeed Gataa, Seyed Mahdi Hassanian, Gordon A Ferns, Majid Khazaei, Amir Avan\",\"doi\":\"10.2174/0113816128337474250311074502\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Despite recent advances in surgical procedures, postoperative peritoneal adhesions are common following major abdominopelvic surgery. Here, the therapeutic potential of Punica granatum var. pleniflora (PGP) on postoperative peritoneal adhesions has been explored in a rat uterine horn adhesion model.</p><p><strong>Method: </strong>Eighteen Albino Wistar female rats were divided into three groups: control group, sham, and treatment group receiving 400 mg/kg/day PGP orally for ten days. An identical surgical technique was employed to induce adhesion of the uterine horn in both the control and treatment groups. At the end of the experiments, all rats were re-operated for evaluation of adhesion. The macroscopic evaluation and fibrotic bands scaling were conducted and inflammation and fibrosis were assessed and graded, microscopically. Additionally, the effect of PGP on inflammation and fibrosis was assessed via PCR, ELISA, and histopathology.</p><p><strong>Results: </strong>PGP could significantly reduce the peritoneal adhesion score (treatment group vs. control group; P<0.001). Histopathological analysis indicated that PGP prevented adhesion formation by suppressing inflammation and fibrosis. Moreover, inflammatory and fibrosis biomarkers were decreased following PGP treatment. Furthermore, rats in the treatment group had significantly lower oxidative stress markers in adhesion tissues when compared to the control group.</p><p><strong>Conclusion: </strong>Oral PGP was associated with reduced peritoneal adhesion formation in rats, postoperatively. This therapy might be an effective and safe strategy for preventing intraperitoneal adhesion after abdominopelvic surgeries.</p>\",\"PeriodicalId\":10845,\"journal\":{\"name\":\"Current pharmaceutical design\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-03-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current pharmaceutical design\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.2174/0113816128337474250311074502\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current pharmaceutical design","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2174/0113816128337474250311074502","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Treatment with Punica granatum var. pleniflora Inhibits Postoperative Adhesion Formation in a Rat Uterine Horn Adhesion Model.
Objective: Despite recent advances in surgical procedures, postoperative peritoneal adhesions are common following major abdominopelvic surgery. Here, the therapeutic potential of Punica granatum var. pleniflora (PGP) on postoperative peritoneal adhesions has been explored in a rat uterine horn adhesion model.
Method: Eighteen Albino Wistar female rats were divided into three groups: control group, sham, and treatment group receiving 400 mg/kg/day PGP orally for ten days. An identical surgical technique was employed to induce adhesion of the uterine horn in both the control and treatment groups. At the end of the experiments, all rats were re-operated for evaluation of adhesion. The macroscopic evaluation and fibrotic bands scaling were conducted and inflammation and fibrosis were assessed and graded, microscopically. Additionally, the effect of PGP on inflammation and fibrosis was assessed via PCR, ELISA, and histopathology.
Results: PGP could significantly reduce the peritoneal adhesion score (treatment group vs. control group; P<0.001). Histopathological analysis indicated that PGP prevented adhesion formation by suppressing inflammation and fibrosis. Moreover, inflammatory and fibrosis biomarkers were decreased following PGP treatment. Furthermore, rats in the treatment group had significantly lower oxidative stress markers in adhesion tissues when compared to the control group.
Conclusion: Oral PGP was associated with reduced peritoneal adhesion formation in rats, postoperatively. This therapy might be an effective and safe strategy for preventing intraperitoneal adhesion after abdominopelvic surgeries.
期刊介绍:
Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field.
Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.