箭毒叶甲醇提取物对 Wistar 大鼠肾脏肝脏的保护作用和抗糖尿病作用

IF 3.3 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE
Oluwaseyi Adegoke Adetunji, Jeremiah Olorunjuwon Olugbami, Ayodeji Mathias Adegoke, Michael Adedapo Gbadegesin, Oyeronke Adunni Odunola
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引用次数: 0

摘要

接触被砷污染的水导致中毒和糖尿病的发生是主要的健康问题。采用治疗措施来解决这些问题的效果有限。传统上,Laportea aestuans(LA)被用于治疗各种疾病。因此,我们研究了雄性 Wistar 大鼠体内 Laportea aestuans(LA)甲醇叶提取物(MeLELA)的肝脏保护/抗糖尿病潜力。将 30 只大鼠(100-150 克)平均分成 6 组:第一组(药物治疗);第二组接受 2.5 毫克/千克亚砷酸钠(SA)治疗,每周三次,连续两周;第三组接受链脲佐菌素(STZ,50 毫克/千克,一次)治疗;第四组每天接受 200 毫克/千克 LA 治疗,连续 14 天;第五组接受 SA 和 LA 治疗;第六组接受 STZ 和 LA 治疗。亚砷酸钠和 STZ 分别诱发肾肝毒性和糖尿病。植物化学筛选、生物标志物/酶活性、血糖水平、微核检测、肾脏、肝脏和胰腺组织学均按照标准程序进行测定。结果表明,SA 和 STZ 处理的动物体内含有大量生物碱、类胡萝卜素和黄酮类化合物。SA和STZ处理组的血清蛋白浓度均显著降低(p < 0.05),而与LA联合处理组的血清蛋白浓度则显著恢复。SA 引起的肌酐/尿素水平显著升高在 LA 的作用下也明显降低。在 SA 和 STZ 治疗组中,LA 可显著降低血清丙氨酸和天门冬氨酸转氨酶活性的升高。LA 能明显降低糖尿病组的血糖升高。此外,LA 还能明显降低 SA 引起的多色微核红细胞的频率。总之,LA 对 SA 诱导的毒性和 STZ 诱导的 Wistar 大鼠糖尿病具有保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of <i>Laportea Aestuans</i> in Wistar Rats.

Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of <i>Laportea Aestuans</i> in Wistar Rats.

Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of <i>Laportea Aestuans</i> in Wistar Rats.

Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of Laportea Aestuans in Wistar Rats.

Toxicities due to exposure to arsenic-contaminated water and the occurrence of diabetes mellitus are major health concerns. Treatment of these concerns using therapeutic measures have recorded limited success. Traditionally, Laportea aestuans (LA) has been used in managing various diseases. Hence, we investigated the reno-hepatoprotective/antidiabetic potentials of methanol leaf extract of LA (MeLELA) in male Wistar rats. Thirty rats (100-150 g) were equally distributed into 6 groups: Group I (vehicle-treated); group II received 2.5 mg/kg sodium arsenite (SA) thrice a week for 2 weeks; group III received streptozotocin (STZ, 50 mg/kg once); group IV received 200 mg/kg LA daily for 14 days; group V received SA and LA; group VI received STZ and LA. Sodium arsenite and STZ induced reno-hepatotoxicity and diabetes, respectively. Phytochemical screening, biomarkers/enzyme activities, blood glucose levels, micronucleus assay, kidney, liver and pancreas histologies were determined according to standard procedures. Alkaloids, carotenoids and flavonoids were present in abundance. Both SA-and STZ-treated groups recorded significant (p < 0.05) reductions in serum protein concentrations, while co-treatment with LA significantly restored the levels. The SA-induced significant increase in creatinine/urea levels were significantly reduced by LA. Co-treatment of each of SA-and STZ-treated groups, respectively, with LA significantly decreased the elevated serum alanine and aspartate aminotransferases' activities. Increased blood glucose level in diabetic group was remarkably lowered by LA. Also, the SA-induced frequency of micronucleated polychromatic erythrocytes was significantly ameliorated by LA. Conclusively, LA is protective against SA-induced toxicity and STZ-induced diabetes in Wistar rats.

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来源期刊
Journal of Evidence-based Integrative Medicine
Journal of Evidence-based Integrative Medicine INTEGRATIVE & COMPLEMENTARY MEDICINE-
CiteScore
5.90
自引率
0.00%
发文量
43
审稿时长
15 weeks
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