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Leila Zarei, Mehri Kouhkan, Rahim Mohammadi, Amir Bolouri,
Volume 22, Issue 1 (4-2020)
Abstract

Background: Wound healing is the interaction of a complex cascade of cellular and biochemical actions leading to the restoration of structural and functional integrity with regaining the strength of injured tissues. Diabetes is effective in delaying the wound healing process in human beings. It has been reported that pyrozilidine derivatives bear antioxidant activity and antioxidant agents that accelerate wound healing process. The aim of the present study was to assess the activity of Methyl 2'-Methyl-1,3-dioxo-1,1',2',3,5',6',7',7a'-octahydrospiro[indene-2,3'-pyrrolizidine]-2' carboxylate (6) on the full-thickness excisional wound healing in diabetic rats. 
Material and Methods: 60 male Wistar rats were randomized into three groups of 20 animals following the creation of the wound. Group 1 (normal control): creation of the wound with no further intervention. Group 2 (diabetic control): induction of diabetes in the animals and creation of the wound with the intraperitoneal administration of 100 microliter DMSO (0.25%) for one week. Group 3 (treatment): induction of diabetes in the animals and creation of the wound with the intraperitoneal administration of 100 microliter of the synthetized agent (60 µg/kg) dissolved in DMSO (0.25%) for one week. Induction of diabetes in the animals of groups 2 and 3 was performed using streptozotocin. Histologic studies were conducted on the days 7, 14 and 21 post wounding. Planimetric studies were carried out on the days 3, 6, 9, 12, 15, 18 and 21 post wounding. 
Results: The histologic studies indicated a significant decrease in inflammatory cells and a noticeable increase in fibroblasts (P<0.05).
Conclusion: It could be concluded that treatment with the synthetized agent (6) could increase wound healing rate in diabetic rats.

Golbano Bolouri, Mehran Ghahramani, Iraj Geraminia, Mahdieh Nassiri Avanaki,
Volume 23, Issue 4 (9-2021)
Abstract

Background: This study aimed to compare the two methods of continuous and interval training for eight weeks on Aplin 13 and fibroblast growth factor in elderly rats.
Materials and Methods: In this study, 30 elderly male rats were randomly divided into three groups of continuous training (n=10), interval training (n=10), and control group (n=10). Interventions were performed for eight weeks. Blood samples (3 cc) were taken from the tails of elderly male rats 72 h before and after the last session of the protocol to evaluate the research variables (Aplin 13 and fibroblast growth factor). One-way analysis of variance was used to analyze the findings, and the Tukey test was utilized for the homogeneity of variance of groups. All statistical tests were performed in SPSS software (version 17) at a significance level of α=0.05.
Results: Aplin 13 had a significant increase in the continuous exercise group (P<0.05). Moreover, the fibroblast growth factor was significantly increased in the continuous exercise group (P<0.05). Aplin 13 had a significant increase in the interval exercise group (P<0.05). Fibroblast growth factor was significantly increased in the interval exercise group (P<0.05). No significant changes were observed in the control group.
Conclusion: The results of this study showed that eight weeks of continuous and interval training caused a significant increase in the levels of Aplin 13 and fibroblast growth factor in elderly male rats. Therefore, these exercises and especially periodic exercises can be used as a suitable way to increase angiogenesis in the elderly.



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