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芦荟减轻了对乙酰氨基酚诱导的肝炎小鼠的肝损伤。

Aloe vera attenuated liver injury in mice with acetaminophen-induced hepatitis.

机构信息

Departments of Physiology, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.

出版信息

BMC Complement Altern Med. 2014 Jul 8;14:229. doi: 10.1186/1472-6882-14-229.

DOI:10.1186/1472-6882-14-229
PMID:25005608
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4227002/
Abstract

BACKGROUND

An overdose of the acetaminophen causes liver injury. This study aims to examine the anti-oxidative, anti-inflammatory effects of Aloe vera in mice with acetaminophen induced hepatitis.

METHODS

Male mice were randomly divided into three groups (n = 8 each). Control group were given orally distilled water (DW). APAP group were given orally N-acetyl-P-aminophenol (APAP) 400 mg/kg suspended in DW. Aloe vera-treated group were given orally APAP and Aloe vera (150 mg/kg) suspended in DW. Twenty-four hours later, the liver was removed to determine hepatic malondialdehyde (MDA), hepatic glutathione (GSH), the number of interleukin (IL)-12 and IL-18 positive stained cells (%) by immunohistochemistry method, and histopathological examination. Then, the serum was collected to determine transaminase (ALT).

RESULTS

In APAP group, ALT, hepatic MDA and the number of IL-12 and IL-18 positive stained cells were significantly increased when compared to control group (1210.50 ± 533.86 vs 85.28 ± 28.27 U/L, 3.60 ± 1.50 vs 1.38 ± 0.15 nmol/mg protein, 12.18 ± 1.10 vs 1.84 ± 1.29%, and 13.26 ± 0.90 vs 2.54 ± 1.29%, P = 0.000, respectively), whereas hepatic GSH was significantly decreased when compared to control group (5.98 ± 0.30 vs 11.65 ± 0.43 nmol/mg protein, P = 0.000). The mean level of ALT, hepatic MDA, the number of IL-12 and IL-18 positive stained cells, and hepatic GSH in Aloe vera-treated group were improved as compared with APAP group (606.38 ± 495.45 vs 1210.50 ± 533.86 U/L, P = 0.024; 1.49 ± 0.64 vs 3.60 ± 1.50 nmol/mg protein, P = 0.001; 5.56 ± 1.25 vs 12.18 ± 1.10%, P = 0.000; 6.23 ± 0.94 vs 13.26 ± 0.90%, P = 0.000; and 10.02 ± 0.20 vs 5.98 ± 0.30 nmol/mg protein, P = 0.000, respectively). Moreover, in the APAP group, the liver showed extensive hemorrhagic hepatic necrosis at all zones while in Aloe vera-treated group, the liver architecture was improved histopathology.

CONCLUSIONS

APAP overdose can cause liver injury. Our result indicate that Aloe vera attenuate APAP-induced hepatitis through the improvement of liver histopathology by decreased oxidative stress, reduced liver injury, and restored hepatic GSH.

摘要

背景

过量的对乙酰氨基酚会导致肝损伤。本研究旨在研究芦荟对乙酰氨基酚诱导的肝炎小鼠的抗氧化、抗炎作用。

方法

雄性小鼠随机分为三组(每组 8 只)。对照组给予口服蒸馏水(DW)。APAP 组给予口服 N-乙酰-P-氨基酚(APAP)400mg/kg 悬浮在 DW 中。芦荟处理组给予口服 APAP 和芦荟(150mg/kg)悬浮在 DW 中。24 小时后,取出肝脏,通过免疫组织化学方法测定肝丙二醛(MDA)、肝谷胱甘肽(GSH)、白细胞介素(IL)-12 和 IL-18 阳性染色细胞数(%),并进行组织病理学检查。然后,收集血清以测定转氨酶(ALT)。

结果

与对照组相比,APAP 组 ALT、肝 MDA 和 IL-12 和 IL-18 阳性染色细胞数显著增加(1210.50±533.86 vs 85.28±28.27U/L、3.60±1.50 vs 1.38±0.15nmol/mg 蛋白、12.18±1.10 vs 1.84±1.29%和 13.26±0.90 vs 2.54±1.29%,P=0.000),而肝 GSH 与对照组相比显著降低(5.98±0.30 vs 11.65±0.43nmol/mg 蛋白,P=0.000)。与 APAP 组相比,芦荟处理组的 ALT、肝 MDA、IL-12 和 IL-18 阳性染色细胞数和肝 GSH 水平均有所改善(606.38±495.45 vs 1210.50±533.86U/L,P=0.024;1.49±0.64 vs 3.60±1.50nmol/mg 蛋白,P=0.001;5.56±1.25 vs 12.18±1.10%,P=0.000;6.23±0.94 vs 13.26±0.90%,P=0.000;和 10.02±0.20 vs 5.98±0.30nmol/mg 蛋白,P=0.000)。此外,在 APAP 组中,肝脏各区域均显示广泛出血性肝坏死,而在芦荟处理组中,肝脏结构得到改善。

结论

APAP 过量可导致肝损伤。我们的结果表明,芦荟通过降低氧化应激、减轻肝损伤和恢复肝 GSH 来减轻 APAP 诱导的肝炎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e9/4227002/857326e2f73d/1472-6882-14-229-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e9/4227002/b4a7757db661/1472-6882-14-229-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e9/4227002/a0a605be9b37/1472-6882-14-229-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e9/4227002/f04d2c96b636/1472-6882-14-229-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e9/4227002/857326e2f73d/1472-6882-14-229-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e9/4227002/b4a7757db661/1472-6882-14-229-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e9/4227002/a0a605be9b37/1472-6882-14-229-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e9/4227002/f04d2c96b636/1472-6882-14-229-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e9/4227002/857326e2f73d/1472-6882-14-229-4.jpg

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