Efficacy and safety assessment of probiotic Bacillus coagulans (Heyndrickxia coagulans) BCP92 for treatment of diarrhea.

IF 2.2 4区 医学 Q3 TOXICOLOGY
Toxicology Research Pub Date : 2024-11-11 eCollection Date: 2024-12-01 DOI:10.1093/toxres/tfae182
Sohel S Shaikh, Snehal Patel, Anis Malik, Aakash Kumar S
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引用次数: 0

Abstract

Objective: Probiotics offer a potentially new therapeutic approach for the treatment of diarrhea. This study aimed to determine the anti-diarrheal activity of Bacillus coagulans BCP92 (MTCC 25460) and its safety assessment (acute and sub-acute toxicity studies) in animal models and cell lines.

Methods: The antidiarrheal activity was studied in mice using a castor oil-induced diarrhea model. In the acute toxicity study, the rats were orally fed 2000 mg/kg (4 × 1011 CFU/g) of B. coagulans BCP92 (MTCC 25460) as a single dose, and for sub-acute toxicity study rats received 250, 500, and 1,000 mg/kg/day for 28 days. At the end of the treatment, body weight, organ weight, food intake, biochemical parameters, hematological parameters, and histopathology were studied. B. coagulans BCP92 is effective against diarrhea by reducing the onset of diarrhea (latency), frequency of defecation, total fecal weight, and percentage of defecation. In-vitro MTT assay was performed on Vero cell lines.

Results: In-vitro MTT assay showed a cytoprotective effect. In acute toxicity study, 2000 mg/kg dose did not cause any alteration in clinical signs, morbidity, or mortality. The findings of the subacute toxicity study showed no alterations in physical appearance and behavioral patterns. Moreover, no significant variations were found in organ weights and hematological and biochemical parameters of the treated groups in the control group. Furthermore, no visible histological changes were observed in the heart, lung, liver, and kidney of the high-dose treatment groups.

Conclusion: Thus, the results of the present study conclude that B. coagulans BCP92 is safe for human use in the treatment of diarrhea.

益生菌凝结芽孢杆菌(Heyndrickxia coagulans)BCP92 治疗腹泻的疗效和安全性评估。
目的:益生菌为治疗腹泻提供了一种潜在的新疗法。本研究旨在确定凝结芽孢杆菌 BCP92(MTCC 25460)的止泻活性及其在动物模型和细胞系中的安全性评估(急性和亚急性毒性研究):采用蓖麻油诱导的腹泻模型对小鼠的止泻活性进行了研究。在急性毒性研究中,给大鼠口服单剂量 2000 毫克/千克(4 × 1011 CFU/克)的 B. coagulans BCP92(MTCC 25460);在亚急性毒性研究中,给大鼠口服 250、500 和 1,000 毫克/千克/天,共 28 天。治疗结束后,对大鼠的体重、器官重量、进食量、生化指标、血液学指标和组织病理学进行了研究。凝结球菌 BCP92 对腹泻有效,能减少腹泻的发生(潜伏期)、排便次数、粪便总重量和排便率。在 Vero 细胞系上进行了体外 MTT 试验:结果:体外 MTT 试验显示了细胞保护作用。在急性毒性研究中,2000 毫克/千克的剂量不会导致任何临床症状、发病率或死亡率的改变。亚急性毒性研究结果表明,动物的体貌和行为模式没有发生变化。此外,处理组与对照组的器官重量、血液学和生化指标也未发现明显变化。此外,在高剂量处理组的心脏、肺、肝脏和肾脏中也没有观察到明显的组织学变化:因此,本研究得出结论,凝结球菌 BCP92 可安全用于人类腹泻的治疗。
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来源期刊
Toxicology Research
Toxicology Research TOXICOLOGY-
CiteScore
3.60
自引率
0.00%
发文量
82
期刊介绍: A multi-disciplinary journal covering the best research in both fundamental and applied aspects of toxicology
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