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表没食子儿茶素没食子酸酯可拮抗顺铂对大鼠睾丸的毒性。

Epigallocatechin-3-gallate counters cisplatin toxicity of rat testes.

机构信息

a Biomedical Sciences Department, Division of Pharmacology, College of Medicine , King Faisal University , Al-Ahsa , Saudi Arabia.

b Department of Pharmacology, Faculty of Medicine , Minia University , El-Minia , Egypt.

出版信息

Pharm Biol. 2017 Dec;55(1):1710-1714. doi: 10.1080/13880209.2017.1322618.

DOI:10.1080/13880209.2017.1322618
PMID:28478745
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6130736/
Abstract

CONTEXT

Epigallocatechin-3-gallate (EG), the main active flavonoid in green tea, has well-known anti-inflammatory, antioxidant, and anti-apoptotic activities.

OBJECTIVE

The EG protection against testicular injury induced by cisplatin was studied in Sprague-Dawley rats.

MATERIALS AND METHODS

Cisplatin (10 mg/kg, i.p) was given as a single injection to rats. EG was given at 40 and 80 mg/kg/day, i.p., for 5 days, starting the same day of cisplatin insult. Serum testosterone, and testicular malondialdehyde, total antioxidant status, nitric oxide, interleukin-6, interleukin-1β, cytochrome C, Bax/Bcl-2 ratio, and caspase-3 were measured. In addition, testicular histopathological examination and immunohistochemical expression of testicular tumour necrosis factor-α were evaluated.

RESULTS

Cisplatin, compared to the control, significantly decreased serum testosterone (6.48 ± 0.7 vs. 50.8 ± 4.91 ng/10 mL), and testicular tissue antioxidant status (17.3 ± 1.21 vs. 64.12 ± 5.4 μmol/g), and significantly increased interleukin-6 (85.81 ± 6.11 vs. 38.2 ± 2.79 pg/100 mg), interleukin-1β (98.09 ± 8.31 vs. 32.52 ± 2.08 pg/100 mg), malondialdehyde (74.5 ± 5.88 vs. 23.8 ± 1.91 nmol/g), nitric oxide (104.98 ± 8.5 vs. 52.68 ± 5.12 nmol/100 mg), cytochrome C (5.97 ± 0.33 vs. 1.6 ± 0.99 ng/mg protein), Bax/Bcl-2 ratio (4.01 ± 0.38 vs. 0.71 ± 0.0), and caspase-3 (3.2 ± 0.21 vs. 0.98 ± 0.08 O.D. 405 nm) in rat testes. EG (40 and 80 mg/kg, respectively) caused significant increases of serum testosterone (33.9 ± 2.89 and 47.88 ± 4.4 ng/10 mL), and testicular antioxidant status (47.1 ± 3.92 and 58.22 ± 3.58 μmol/g), and significant decreases of interleukin-6 (57.39 ± 4.2 and 48.18 ± 3.98 pg/100 mg), interleukin-1β (65.12 ± 5.88 and 41.96 ± 3.51 pg/100 mg), malondialdehyde (42.3 ± 3.9 and 28.67 ± 2.49 nmol/g), nitric oxide (70.6 ± 6.79 and 61.31 ± 5.18 nmol/100 mg), cytochrome C (3.4 ± 0.27 and 2.21 ± 0.18 ng/mg protein), Bax/Bcl-2 ratio (1.49 ± 0.14 and 1.1 ± 0.09), and caspase-3 (2.1 ± 0.17 and 1.48 ± 0.13 O.D. 405 nm) in testes of cisplatin-treated rats. Additionally, both doses of EG significantly ameliorated the histopathological injury and reduced tumour necrosis factor-α expression in rat testes.

CONCLUSION

EG can afford testicular protection in cisplatin-challenged rats by its antioxidant, antinitrative, anti-inflammatory and antiapoptotic effects.

摘要

背景

表没食子儿茶素没食子酸酯(EG)是绿茶中的主要活性类黄酮,具有众所周知的抗炎、抗氧化和抗凋亡作用。

目的

研究 EG 对顺铂诱导的大鼠睾丸损伤的保护作用。

材料和方法

顺铂(10mg/kg,腹腔注射)单次注射给予大鼠。EG 以 40 和 80mg/kg/天的剂量腹腔注射 5 天,从顺铂损伤的同一天开始。测量血清睾酮和睾丸丙二醛、总抗氧化状态、一氧化氮、白细胞介素-6、白细胞介素-1β、细胞色素 C、Bax/Bcl-2 比值和半胱天冬酶-3。此外,评估了睾丸组织病理学检查和肿瘤坏死因子-α的免疫组织化学表达。

结果

与对照组相比,顺铂显著降低了血清睾酮(6.48±0.7 与 50.8±4.91ng/10mL)和睾丸组织抗氧化状态(17.3±1.21 与 64.12±5.4μmol/g),显著增加了白细胞介素-6(85.81±6.11 与 38.2±2.79pg/100mg)、白细胞介素-1β(98.09±8.31 与 32.52±2.08pg/100mg)、丙二醛(74.5±5.88 与 23.8±1.91nmol/g)、一氧化氮(104.98±8.5 与 52.68±5.12nmol/100mg)、细胞色素 C(5.97±0.33 与 1.6±0.99ng/mg 蛋白)、Bax/Bcl-2 比值(4.01±0.38 与 0.71±0.0)和半胱天冬酶-3(3.2±0.21 与 0.98±0.08O.D.405nm)在大鼠睾丸中的表达。EG(40 和 80mg/kg)分别导致血清睾酮(33.9±2.89 和 47.88±4.4ng/10mL)和睾丸抗氧化状态(47.1±3.92 和 58.22±3.58μmol/g)显著增加,白细胞介素-6(57.39±4.2 和 48.18±3.98pg/100mg)、白细胞介素-1β(65.12±5.88 和 41.96±3.51pg/100mg)、丙二醛(42.3±3.9 和 28.67±2.49nmol/g)、一氧化氮(70.6±6.79 和 61.31±5.18nmol/100mg)、细胞色素 C(3.4±0.27 和 2.21±0.18ng/mg 蛋白)、Bax/Bcl-2 比值(1.49±0.14 和 1.1±0.09)和半胱天冬酶-3(2.1±0.17 和 1.48±0.13O.D.405nm)在顺铂处理的大鼠睾丸中显著降低。此外,EG 的两种剂量均显著改善了大鼠睾丸的组织病理学损伤,并降低了肿瘤坏死因子-α的表达。

结论

EG 通过其抗氧化、抗硝化、抗炎和抗凋亡作用,可为顺铂挑战的大鼠提供睾丸保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd7e/6130736/3babff9833be/IPHB_A_1322618_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd7e/6130736/0ab0dab53b4e/IPHB_A_1322618_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd7e/6130736/5d115bc54084/IPHB_A_1322618_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd7e/6130736/72fc7bcbd107/IPHB_A_1322618_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd7e/6130736/3babff9833be/IPHB_A_1322618_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd7e/6130736/0ab0dab53b4e/IPHB_A_1322618_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd7e/6130736/5d115bc54084/IPHB_A_1322618_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd7e/6130736/72fc7bcbd107/IPHB_A_1322618_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd7e/6130736/3babff9833be/IPHB_A_1322618_F0004_C.jpg

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