Tarçın Ekstraktı İle Tedavi Edilen Diyabetik Sıçanların Mide Dokusunda Somatostatinin İmmunohistokimyasal Dağılımı
Diyabet, kronik metabolik bir bozukluk olduğu gibi aynı zamanda da artmış bir oksidatif stres durumudur. Çalışmamızda immunohistokimyasal teknik kullanarak tarçın uygulanan streptozotosin ile diabet oluşturulan ratların mide dokusundaki somatostatinin salınımını inceledik. Çalışmada 30 adet Sprague Dawley cinsi erkek rat kullanıldı. Deney grupları kontrol, sham, tarçın, diyabet ve diyabet + tarçın olarak 5 gruba ayrıldı. Kontrol grubuna herhangi bir uygulama yapılmadı, sham grubuna intraperitoneal (i.p.) olarak 50 mg/kg sodyum sitrate uygulandı. Diyabet ve diyabet + tarçın gruplarına i.p. 50 mg/kg STZ enjeksiyonu yapılarak diabet oluşturuldu. Tarçın ve diyabet + tarçın gruplarına tarçın ekstraktı 200 mg/kg olacak şekilde oral gavaj yolu ile 14 gün verildi. Somatostatinin immunoreaktivitesini belirlemek için streptavidin-biotin-peroxidase metotu uygulandı. Mide dokularının normal histolojik yapısını incelemek için Crossman’ın üçlü boyama yöntemi ve Hematoksilen-Eosin boyaması uygulandı. Kontrol, sham ve tarçın gruplarındaki somotostatin immunoreaktivitesi, diyabet ve diyabet + tarçın gruplarından daha güçlü olduğu tesbit edildi. Diyabet ve diyabet + tarçın gruplarında mide dokusunun kardia, fundus ve pilor mukozasında zayıf immunoreaktivite bulunurken tarçın, sham ve kontrol gruplarında güçlü immunoreaktivite bulundu. Ayrıca tüm gruplar parietal ve prensipal hücre sayıları bakımından karşılaştırıldığında istatiksel olarak anlamlı bulundu (P
Immunohistochemical Distribution of Somatostatin in Gastric Tissue of Diabetic Rats Treated with Cinnamon Extract
Diabetes is a chronic metabolic disorder, as well as a situation of increased oxidative stress. We examined the distribution of somatostatin in gastrictissues of cinnamon extract treated streptozotocin-induced diabetic rats using the immunohistochemistry technique. A total of 30 male SpragueDawley rats were used in the study. The rats were assigned to five groups as control, sham, cinnamon, diabetes and diabetes + cinnamon. Noapplication was made to the control group, the sham group received intraperitoneally (i.p.) 50 mg/kg sodium citrate, and diabetes was inducedby i.p. injection of 50 mg/kg STZ in diabetes and diabetes + cinnamon groups. Cinnamon extracts were then given to cinnamon and diabetes+ cinnamon groups by oral gavage at a dose of 200 mg/kg for 14 days. The streptavidin-biotin-peroxidase method was used to determine theimmunoreactivity of somatostatin. Gastric tissue sections were prepared and stained by Crossman’s triple and Hematoxylin-Eosin staining in orderto examine histological structure of the gastric tissue. We determined that somatostatin immunoreactivity of the control, sham and cinnamongroups was stronger than for the diabetes, and diabetes + cinnamon groups. While a weak immunoreactivity was found in the cardia, fundusand pyloric mucosa of the gastric tissue in the diabetes and diabetes + cinnamon groups, a strong immunoreactivity was found in the cinnamon,sham, and control groups. Also, a statistically significant was observed when all groups compared in terms of count of parietal and principal cells(P
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