栀子提取物可减轻对乙酰氨基酚引起的小鼠肝损伤。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-19 DOI:10.1186/s12906-024-04676-y
Peenaprapa Tangpradubkiat, Maneerat Chayanupatkul, Pornpen Werawatganone, Kanjana Somanawat, Prasong Siriviriyakul, Naruemon Klaikeaw, Duangporn Werawatganon
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引用次数: 0

摘要

背景:对乙酰氨基酚(APAP)引起的肝毒性可能会危及生命。栀子果提取物(GJE)的主要活性成分是基尼泊苷(Gen),它具有抗炎和抗氧化特性,可能有助于解决APAP诱导的肝毒性的潜在发病机制。本研究旨在评估 GJE 在 APAP 诱导的肝毒性小鼠模型中的作用:将 24 只雄性 ICR 小鼠分为 4 组(n = 6/组):[1] 对照组,小鼠给予蒸馏水;[2] APAP 组,小鼠接受单剂量 600 mg/kg APAP;[3] APAP + 低剂量 GJE 组,小鼠接受 APAP 后 30 分钟再接受 2 剂低剂量 GJE(0.44 g/kg/dose, containing Gen 100 mg/kg/dose); [4] APAP + 高剂量 GJE 组,小鼠接受 APAP 后,再接受 2 次高剂量 GJE (0.88 g/kg/dose, containing Gen 200 mg/kg/dose)。所有小鼠均在施用 APAP 24 小时后安乐死。使用肝组织进行组织学检查,并测量谷胱甘肽(GSH)和丙二醛(MDA)的水平。血清用于测定谷丙转氨酶(ALT)和炎症细胞因子(肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6))的水平:结果:肝组织病理学显示 APAP 组存在中度至重度肝坏死炎症,而两个治疗组都只有轻度坏死炎症。与对照组相比,APAP 组的血清 ALT 水平明显升高,但经过低剂量和高剂量 GJE 治疗后,ALT 水平明显降低。APAP 组血清 TNF- α 水平明显高于对照组,但在大剂量 GJE 治疗后明显降低(分别为 135.5 ± 477.2 vs. 35.5 ± 25.8 vs. 74.7 ± 47.2 vs. 41.4 ± 50.8 pg/mL)。血清 IL-6 也有类似的变化。与对照组相比,APAP 组的肝脏 GSH 水平明显较低,但低剂量和高剂量 GJE 治疗后肝脏 GSH 水平均明显升高(分别为 19.9 ± 4.5 vs. 81.5 ± 12.4 vs. 71.4 ± 7.8 vs. 82.6 ± 6.6 nmol/mg 蛋白)。相反,与对照组相比,APAP 组的肝脏 MDA 水平明显升高,但大剂量 GJE 治疗后则明显降低(分别为 108.6 ± 201.5 vs. 40.5 ± 18.0 vs. 40.5 ± 16.8 nmol/mg 蛋白):结论:茉莉果提取物可以减轻 APAP 引起的肝毒性,这可能是由于它具有抗炎和抗氧化特性。
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Gardenia jasminoides extract mitigates acetaminophen-induced liver damage in mice.

Background: Acetaminophen (APAP)-induced hepatotoxicity is a potentially life-threatening condition. Gardenia jasminoides fruit extract (GJE), which contains geniposide (Gen) as its major active constituent, possesses anti-inflammatory and antioxidant properties and may help address the underlying pathogenesis of APAP-induced hepatotoxicity. This study aimed to evaluate the effects of GJE in a mouse model of APAP-induced hepatotoxicity.

Methods: Twenty-four male ICR mice were divided into 4 groups (n = 6/group): [1] Control group, mice were given distilled water; [2] APAP group, mice received a single dose of 600 mg/kg APAP; [3] APAP + low-dose GJE group, mice received APAP followed 30 min later by 2 doses of low-dose GJE (0.44 g/kg/dose, containing Gen 100 mg/kg/dose) 8 h apart; [4] APAP + high-dose GJE group, mice received APAP followed by 2 doses of high-dose GJE (0.88 g/kg/dose, containing Gen 200 mg/kg/dose). All mice were euthanized 24 h after APAP administration. Liver tissue was used for histological examination and to measure glutathione (GSH) and malondialdehyde (MDA) levels. Serum was used to determine levels of ALT and inflammatory cytokines (tumor necrosis factor- α (TNF-α) and interleukin-6 (IL-6)).

Results: Liver histopathology showed moderate to severe hepatic necroinflammation in the APAP group, whereas only mild necroinflammation was observed in both treatment groups. Serum ALT levels were significantly elevated in the APAP group compared to the control group but were significantly reduced after low- and high-dose GJE treatment. Serum TNF- α levels were significantly higher in the APAP group than in the control group and were significantly lower after high-dose GJE treatment (135.5 ± 477.2 vs. 35.5 ± 25.8 vs. 74.7 ± 47.2 vs. 41.4 ± 50.8 pg/mL, respectively). Serum IL-6 followed a similar pattern. Hepatic GSH levels were significantly lower in the APAP group compared to the control group but significantly increased after both low- and high-dose GJE treatment (19.9 ± 4.5 vs. 81.5 ± 12.4 vs. 71.4 ± 7.8 vs. 82.6 ± 6.6 nmol/mg protein, respectively). Conversely, hepatic MDA levels were significantly elevated in the APAP group compared with the control group but significantly decreased after high-dose GJE treatment (108.6 ± 201.5 vs. 40.5 ± 18.0 vs. 40.5 ± 16.8 nmol/mg protein, respectively).

Conclusions: Treatment with G. jasminoides fruit extract can alleviate APAP-induced hepatotoxicity, likely through its anti-inflammatory and antioxidant properties.

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