TY - JOUR
T1 - Intraperitoneal Administration of Telmisartan Prevents Postsurgical Adhesion Band Formation
AU - Arjmand, Mohammad Hassan
AU - Zahedi-Avval, Farnaz
AU - Barneh, Farnaz
AU - Mousavi, Seyed Hadi
AU - Asgharzadeh, Fereshteh
AU - Hashemzehi, Milad
AU - Soleimani, Atena
AU - Avan, Amir
AU - Fakhraie, Maryam
AU - Nasiri, Seyedeh Najibeh
AU - Mehraban, Saeedeh
AU - Ferns, Gordon A.
AU - Ryzhikov, Mikhail
AU - Jafari, Mohieddin
AU - Khazaei, Majid
AU - Hassanian, Seyed Mahdi
N1 - Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2020/4
Y1 - 2020/4
N2 - Background: Angiotensin II receptor blockers (ARBs) have a potential role in reducing inflammation and fibrosis. We have integrated systems and molecular biology approaches to investigate the therapeutic potential of ARBs in preventing postsurgical adhesion band formation. Material and methods: we have followed the ARRIVE guidelines point by point during experimental studies. Telmisartan (1 and 9 mg/kg), valsartan (1 and 9 mg/kg), and losartan (1 and 10 mg/kg) were administered intraperitoneally in different groups of male albino Wistar rat. After 7 d of treatment, macroscopic evidence and score of fibrotic bands based on scaling methods was performed. Moreover, the anti-inflammatory and antifibrosis effects of telmisartan on reduction of fibrotic bands were investigated by using histopathology, ELISA, and real-time polymerase chain reaction methods. Results: Telmisartan, but not losartan or valsartan, prevented the frequency as well as the stability of adhesion bands. Telmisartan appears to elicit anti-inflammatory responses by attenuating submucosal edema, suppressing proinflammatory cytokines, decreasing proinflammatory cell infiltration, and inhibiting oxidative stress at the site of peritoneal surgery. We also showed that telmisartan prevents fibrotic adhesion band formation by reducing excessive collagen deposition and suppression of profibrotic genes expression at the peritoneum adhesion tissues. Conclusions: These results support the potential application of telmisartan in preventing postsurgical adhesion band formation by inhibiting key pathologic responses of inflammation and fibrosis in postsurgery patients.
AB - Background: Angiotensin II receptor blockers (ARBs) have a potential role in reducing inflammation and fibrosis. We have integrated systems and molecular biology approaches to investigate the therapeutic potential of ARBs in preventing postsurgical adhesion band formation. Material and methods: we have followed the ARRIVE guidelines point by point during experimental studies. Telmisartan (1 and 9 mg/kg), valsartan (1 and 9 mg/kg), and losartan (1 and 10 mg/kg) were administered intraperitoneally in different groups of male albino Wistar rat. After 7 d of treatment, macroscopic evidence and score of fibrotic bands based on scaling methods was performed. Moreover, the anti-inflammatory and antifibrosis effects of telmisartan on reduction of fibrotic bands were investigated by using histopathology, ELISA, and real-time polymerase chain reaction methods. Results: Telmisartan, but not losartan or valsartan, prevented the frequency as well as the stability of adhesion bands. Telmisartan appears to elicit anti-inflammatory responses by attenuating submucosal edema, suppressing proinflammatory cytokines, decreasing proinflammatory cell infiltration, and inhibiting oxidative stress at the site of peritoneal surgery. We also showed that telmisartan prevents fibrotic adhesion band formation by reducing excessive collagen deposition and suppression of profibrotic genes expression at the peritoneum adhesion tissues. Conclusions: These results support the potential application of telmisartan in preventing postsurgical adhesion band formation by inhibiting key pathologic responses of inflammation and fibrosis in postsurgery patients.
KW - Angiotensin receptor blockers
KW - Fibrosis
KW - Inflammation
KW - Postsurgical adhesion band formation
KW - Telmisartan
UR - http://www.scopus.com/inward/record.url?scp=85077395563&partnerID=8YFLogxK
U2 - 10.1016/j.jss.2019.10.029
DO - 10.1016/j.jss.2019.10.029
M3 - Article
C2 - 31923833
AN - SCOPUS:85077395563
SN - 0022-4804
VL - 248
SP - 171
EP - 181
JO - Journal of Surgical Research
JF - Journal of Surgical Research
ER -