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芦荟提取物对阿霉素诱导的小鼠卵巢卵泡和基质细胞变性的保护作用。

Protective effects of Aloe vera extract against doxorubicin-induced degeneration in ovarian follicles and stromal cells in mice.

作者信息

Assis E I T de, Godinho A N, Freire J M O, Lima Neto M F de, Costa J J N, Souza A L P, Monte A P O do, Matos M H T, Sousa A L M de, Silva J R V, Silva A W B

机构信息

Laboratório de Biotecnologia e Fisiologia da Reprodução, Universidade Federal do Ceará, Sobral, CE, Brasil.

Núcleo de Pesquisa em Experimentação Animal, Universidade Federal do Ceará, Sobral, CE, Brasil.

出版信息

Braz J Med Biol Res. 2025 Jun 16;58:e14402. doi: 10.1590/1414-431X2025e14402. eCollection 2025.

DOI:10.1590/1414-431X2025e14402
PMID:40531753
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12172158/
Abstract

The present study aimed to evaluate the protective effects of Aloe vera on doxorubicin (DOX)-induced degeneration in ovarian follicles and stromal cells in mice. Mice (n=48) were randomly divided into six groups. The positive control group mice received pretreatment of N-acetylcysteine orally (po), followed by a single intraperitoneal (ip) dose of DOX after 1 h (NAC+DOX). The negative control group mice were pre-treated with saline (po) and administered a single DOX dose (ip) after 1 h (SAL+DOX). The other groups of mice were pre-treated with different concentrations (0.1, 1.0, or 10.0 mg/kg; po) of Aloe vera and then received a single dose of DOX (ip) after 1 h (AV0.1+DOX, AV1.0+DOX, and AV10.0+DOX). The control group received saline po and ip (SAL+SAL). Aloe vera was administered once daily for 3 consecutive days. On the fourth day, the ovaries were processed for histological analysis, immunohistochemistry, and real-time PCR (mRNA for superoxide dismutase (SOD), catalase (CAT), nuclear factor erythroid 2-related factor 2 (NRF2), and tumor necrosis factor-α (TNF-α). Results showed that 0.1 and 1.0 mg/kg Aloe vera protected ovarian follicles and stromal density against DOX-induced degeneration. Furthermore, 0.1 and 1.0 mg/kg Aloe vera reduced TNF-α protein expression and increased NRF2, SOD, and CAT mRNA levels. In conclusion, 0.1 and 1.0 mg/kg Aloe vera had protective effects against DOX-induced degeneration in ovarian follicles and stromal cells in mice.

摘要

本研究旨在评估芦荟对阿霉素(DOX)诱导的小鼠卵巢卵泡和基质细胞变性的保护作用。将48只小鼠随机分为六组。阳性对照组小鼠口服N-乙酰半胱氨酸进行预处理,1小时后腹腔注射单次剂量的DOX(NAC+DOX)。阴性对照组小鼠用生理盐水预处理,1小时后腹腔注射单次剂量的DOX(SAL+DOX)。其他几组小鼠用不同浓度(0.1、1.0或10.0mg/kg;口服)的芦荟进行预处理,1小时后腹腔注射单次剂量的DOX(AV0.1+DOX、AV1.0+DOX和AV10.0+DOX)。对照组小鼠口服和腹腔注射生理盐水(SAL+SAL)。连续3天每天给药一次芦荟。在第4天,对卵巢进行组织学分析、免疫组织化学和实时PCR(超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、核因子红细胞2相关因子2(NRF2)和肿瘤坏死因子-α(TNF-α)的mRNA)检测。结果表明,0.1和1.0mg/kg的芦荟可保护卵巢卵泡和基质密度免受DOX诱导的变性。此外,0.1和1.0mg/kg的芦荟可降低TNF-α蛋白表达,并提高NRF2、SOD和CAT的mRNA水平。总之,0.1和1.0mg/kg的芦荟对DOX诱导的小鼠卵巢卵泡和基质细胞变性具有保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/d713b50feb21/1414-431X-bjmbr-58-e14402-gf007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/334f34ab4c70/1414-431X-bjmbr-58-e14402-gf001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/c5c46dda78ea/1414-431X-bjmbr-58-e14402-gf002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/45251e63df93/1414-431X-bjmbr-58-e14402-gf003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/5cdb49f926a5/1414-431X-bjmbr-58-e14402-gf004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/8697b6e52786/1414-431X-bjmbr-58-e14402-gf005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/beb62ce1617c/1414-431X-bjmbr-58-e14402-gf006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/d713b50feb21/1414-431X-bjmbr-58-e14402-gf007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/334f34ab4c70/1414-431X-bjmbr-58-e14402-gf001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/c5c46dda78ea/1414-431X-bjmbr-58-e14402-gf002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/45251e63df93/1414-431X-bjmbr-58-e14402-gf003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/5cdb49f926a5/1414-431X-bjmbr-58-e14402-gf004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/8697b6e52786/1414-431X-bjmbr-58-e14402-gf005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/beb62ce1617c/1414-431X-bjmbr-58-e14402-gf006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd9/12172158/d713b50feb21/1414-431X-bjmbr-58-e14402-gf007.jpg

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