Possible contribution of nitric oxide and prostaglandin in the protective effect of angiotensin (1-7) against stress induced gastric ulceration in adult male albino rats

被引:1
|
作者
Hassan, M. K. A. [1 ]
Aziz, N. M. [1 ]
Shaaban, M. A. E. [2 ]
Rifaai, R. A. [3 ]
机构
[1] Menia Univ, Dept Physiol, Fac Med, Al Minya 61111, Egypt
[2] AL Azhar Univ, Dept Physiol, Fac Med, Assiut, Egypt
[3] Menia Univ, Dept Histol, Fac Med, Al Minya, Egypt
来源
BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY | 2016年 / 117卷 / 12期
关键词
angiotensin (1-7); cold restraint stress; Nitric oxide; prostaglandin E-2; caspase; 3; RESTRAINT STRESS; MUCOSAL DAMAGE; COLD STRESS; INHIBITION; SECRETION; LIGATION; HYDROGEN; RECEPTOR; ULCERS; AXIS;
D O I
10.4149/BLL_2016_137
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To assess the gastro-protective potential of the angiotensin (Ang-) (1-7) on the gastric secretion and ulceration induced by cold restraint stress (CRS) in adult male rats and the possible contribution of nitric oxide and prostaglandin E-2. Rats were pylorically ligated and divided randomly into the following groups (8 rats each): control, cold-restraint stressed (CRS), stressed Ang-(1-7) treated, stressed L-NNA-Ang-(1-7) treated, stressed Indo-Ang-(1-7) treated groups. Our results revealed that Ang-(1-7) pre-treatment proved to be protective against development of ulcerative lesions in CRS model as evidenced by histological examination and the reduction of the ulcer index and this could be mediated through reduction of free and total acidity and pepsin concentration of gastric secretion with significantly decreased lipid peroxidation and increased the gastric protective nitric oxide and prostaglandin E2 levels. Furthermore, Ang-(1-7) pre-treatment has anti-apoptotic effect, evident by its down-regulation of the CRS induced over-expression of the gastric caspase 3. In addition, the gastro-protective effects of Ang-(1-7) were significantly attenuated by co-administration with L-NNA or indomethacin. In conclusion, Ang-(1-7) can be considered a potential therapeutic agent to protect against the major clinical challenge of gastric injury resulting from stress. Nitric oxide and prostaglandin E2 seem to contribute to the Ang-(1-7)'s gastro-protective effect (Tab. 2, Fig. 5, Ref. 35). Text in PDF www.elis.sk.
引用
收藏
页码:715 / 721
页数:7
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