Acute oral toxicity evaluation of synbiotic mixture containing Streptococcus salivarius K12 and Musa acuminata aqueous peel extract in Sprague-Dawley rats.

IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Journal of Ayurveda and Integrative Medicine Pub Date : 2024-12-15 DOI:10.1016/j.jaim.2024.101037
Aalina Sakiinah Mohd Fuad, Mohd Hafiz Arzmi, Muhammad Ekmal Bakar, Izatus Shima Taib, Fazle Khuda, Nurrul Shaqinah Nasruddin
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Abstract

Background: The combination of S. salivarius K12 and M. acuminata are being used as synbiotic, but its safety evaulation is required.

Objective: This study aimed to determine the LD50 of synbiotic containing probiotic Streptococcus salivarius K12 and prebiotic Musa acuminata peel extract.

Materials and methods: The determination of LD50 is done according to the Acute Oral Toxicity test No. 425 (AOT425). For limit test, five female Sprague Dawley rats were given a limit dose of 2000 mg/kg of the synbiotic mixture once orally, and observed for 12 days. For subacute toxicity test, twenty female Sprague Dawley rats were randomised into 4 groups (n = 5). Control group received saline, others received synbiotic mixture at doses 175 mg/kg, 550 mg/kg, and 2000 mg/kg, respectively, and observed for 14 days. Animals were euthanised on day-15, blood was collected, and subjected to haematological and biochemical analyses. Kidney and liver were preserved for histopathological examination.

Result: No significant changes on the average body weight of the animals throughout the study. Haematological parameters and biochemical analysis do not depict any changes related to acute toxicity. Histopathology analysis depicted mild changes on kidney and liver.

Conclusion: Based on the data, the LD50 of the synbiotic formulation is higher than 2000 mg/kb, with no sign of acute toxicity observed on all parameters.

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唾液链球菌K12与荆芥水剥提取物复合制剂对sd大鼠急性口服毒性评价。
背景:唾液链球菌K12与尖锐棘球菌联合作为合生剂已被广泛应用,但其安全性评价尚待进一步研究。目的:测定含益生菌唾液链球菌K12和益生元沙棘皮提取物的合成菌的LD50。材料和方法:LD50的测定参照急性口服毒性试验第425号(AOT425)。限药试验方法:雌性大鼠5只,按限药剂量2000 mg/kg口服1次,观察12 d。亚急性毒性试验选取雌性sd大鼠20只,随机分为4组(n = 5),对照组给予生理盐水,对照组给予175 mg/kg、550 mg/kg、2000 mg/kg剂量的合成制剂,观察14 d。在第15天对动物实施安乐死,采集血液并进行血液学和生化分析。保留肾脏和肝脏进行组织病理学检查。结果:在整个研究过程中,动物的平均体重没有明显变化。血液学参数和生化分析没有描述任何与急性毒性有关的变化。组织病理学分析显示肾脏和肝脏轻度改变。结论:合成制剂的LD50均大于2000 mg/kb,各项指标均无急性毒性。
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来源期刊
Journal of Ayurveda and Integrative Medicine
Journal of Ayurveda and Integrative Medicine INTEGRATIVE & COMPLEMENTARY MEDICINE-
CiteScore
4.70
自引率
12.50%
发文量
136
审稿时长
30 weeks
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