Probiotic Lactobacillus acidophilus FNCC 0051 Improves Pancreatic Histopathology in Streptozotocin-induced Type-1 Diabetes Mellitus Rats

M. Sariyanti, Tiara Ayoe Andita, Noor Diah Erlinawati, Elvira Yunita, A. A. Nasution, Kartika Sari, Nikki Aldi Massardi, Sylvia Rianissa Putri
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Abstract

BACKGROUND: Intestinal microbial dysbiosis and its metabolites can affect the immune activity of intestinal mucosal cells, causing insulitis and pancreatic β-cell death. Probiotic Lactobacillus acidophilus plays an important role in reducing inflammatory cytokines, hence improves oxidative stress that affects pancreatic β-cell apoptosis. Current study examined the feature of pancreatic histopathology affected by the administration of probiotic L. acidophilus in rats with type-1 diabetes mellitus (DM) induced by streptozotocin (STZ).METHODS: Twelve rats were induced by STZ at double dose of 50 mg/kgBB before administered with probiotic L. acidophilus at a dose of 1.5x10 8 or 1.5x10 9 CFU/mL/day, while other 4 rats were used as control. After 21 days of the L. acidophilus treatment, the average of fasting blood glucose (FBG) levels of rats were measured, then the pancreatic histopathology was assessed to evaluate the degree of insulitis in islet of Langerhans.RESULTS: The induction of STZ had been succeeded to increase blood glucose levels, which indicate DM condition. The highest FBG level after 21 days of treatment was found in DM group with glucose level of 512±81.51 mg/dL. The administration of probiotic L. acidophilus during 21 days treatment at both dose 1.5x10 8 and 1.5x10 9 CFU/mL/day significantly improved pancreatic histopathology (p=0.04 and p=0.034, respectively), with significant decrease on insulitis scores compared to DM group.CONCLUSION: The administration of L. acidophilus at both dose of 1.5x10 8 and 1.5x10 9 CFU/mL/day for 21 days can improve pancreatic histopathology of type-1 DM rats induced by STZ, therefore probiotic L. acidophilus may be potential as supplementation treatment for type-1 DM.KEYWORDS: Lactobacillus acidophilus, pancreatic histopathology, streptozotocin, type-1 diabetes mellitus
益生菌嗜酸乳杆菌FNCC 0051改善链脲佐菌素诱导的1型糖尿病大鼠胰腺组织病理学
背景:肠道微生物生态失调及其代谢产物可影响肠粘膜细胞的免疫活性,引起胰岛素炎和胰腺β细胞死亡。益生菌嗜酸乳杆菌在减少炎症细胞因子中发挥重要作用,从而改善影响胰腺β细胞凋亡的氧化应激。本研究观察了链脲佐菌素(STZ)诱导的1型糖尿病(DM)大鼠胰脏组织病理学变化与益生菌嗜酸乳杆菌(L. acidophilus)的关系。方法:12只大鼠以50 mg/kgBB双剂量STZ诱导,然后分别给予1.5 × 10 8或1.5 × 10 9 CFU/mL/d益生菌嗜酸乳杆菌,其余4只大鼠作为对照。经嗜酸乳杆菌治疗21 d后,测定各组大鼠平均空腹血糖(FBG)水平,并进行胰腺组织病理学检查,评价朗格汉斯岛胰岛素炎症程度。结果:STZ诱导成功,血糖水平升高,提示糖尿病。治疗21 d后,DM组血糖水平最高,为512±81.51 mg/dL。在21天的治疗中,1.5 × 10 8和1.5 × 10 9 CFU/mL/天的剂量均显著改善了胰腺组织病理学(p=0.04和p=0.034),与DM组相比,胰岛素评分显著降低。结论:嗜酸乳杆菌1.5 × 10 8和1.5 × 10 9 CFU/mL/d连续21 d均能改善STZ诱导的1型DM大鼠胰腺组织病理学,因此嗜酸乳杆菌可能是1型DM的潜在补充治疗。关键词:嗜酸乳杆菌,胰腺组织病理学,链脲佐菌素,1型糖尿病
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