Ernando I T de Assis, Venância A N Azevedo, Miguel F De Lima Neto, Francisco C Costa, Laís R F M Paulino, Alane P O Do Monte, Maria H T Matos, Alana N Godinho, Jordânia M O Freire, Ana L P Souza, José R V Silva, Anderson W B Silva
{"title":"芦荟对阿霉素诱导小鼠卵巢毒性的体外保护作用。","authors":"Ernando I T de Assis, Venância A N Azevedo, Miguel F De Lima Neto, Francisco C Costa, Laís R F M Paulino, Alane P O Do Monte, Maria H T Matos, Alana N Godinho, Jordânia M O Freire, Ana L P Souza, José R V Silva, Anderson W B Silva","doi":"10.1080/10520295.2025.2537829","DOIUrl":null,"url":null,"abstract":"<p><p>The present study investigated the protective effect of <i>Aloe vera</i> extract against the toxic effects of doxorubicin (DOX) on mice ovaries cultured in vitro. Female <i>Swiss</i> mice with regular estrous cycle were used. The animals (n = 48) had their ovaries collected and cultured individually in a 24-well plate at 37.5°C in 5% CO<sub>2</sub> for 6 days. The ovaries were culture DMEM<sup>+</sup> alone or supplemented with DOX (0.3 μg/ml), as well as both DOX and <i>Aloe vera</i> (5%, 10%, 25%, or 50%). After culture, ovaries were fixed for histological analysis (follicle morphology, growth and activation, extracellular matrix (ECM) configuration and stromal cell density), immunohistochemistry (<i>TNF-α</i> expression) or stored at - 80°C to evaluate the levels of mRNA for superoxide dismutase (<i>SOD</i>), catalase (<i>CAT</i>), nuclear factor-erythroid 2-related factor 2 (<i>NRF2</i>) and tumoral necrosis factor-α (<i>TNF-α</i>) by real-time PCR. The results showed that ovaries cultured with DOX had a lower percentage of normal follicles and reduced stromal cell density, but when <i>Aloe vera</i> extract was added to the culture medium, there was a protective effect on the ovarian structure against the deleterious effects of DOX. In addition, ovaries cultured with both DOX and <i>Aloe vera</i> (10 and 25%) had reduced <i>TNF-α</i> immunostaining and increased expression of mRNA for antioxidant enzymes (<i>SOD</i>, <i>CAT</i>, and <i>NRF2</i>). In conclusion, <i>Aloe vera</i> is associated with a protective effect on ovarian follicles and stromal cells against DOX-induced toxicity. Therefore, <i>Aloe vera</i> has great potential to preserve fertility in patients undergoing chemotherapy treatment, which often cause irreversible damage to oocytes.</p>","PeriodicalId":8970,"journal":{"name":"Biotechnic & Histochemistry","volume":" ","pages":"381-392"},"PeriodicalIF":1.4000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Protective <i>in vitro</i> effects of <i>Aloe vera</i> on doxorubicin-induced ovarian toxicity in mice.\",\"authors\":\"Ernando I T de Assis, Venância A N Azevedo, Miguel F De Lima Neto, Francisco C Costa, Laís R F M Paulino, Alane P O Do Monte, Maria H T Matos, Alana N Godinho, Jordânia M O Freire, Ana L P Souza, José R V Silva, Anderson W B Silva\",\"doi\":\"10.1080/10520295.2025.2537829\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The present study investigated the protective effect of <i>Aloe vera</i> extract against the toxic effects of doxorubicin (DOX) on mice ovaries cultured in vitro. Female <i>Swiss</i> mice with regular estrous cycle were used. The animals (n = 48) had their ovaries collected and cultured individually in a 24-well plate at 37.5°C in 5% CO<sub>2</sub> for 6 days. The ovaries were culture DMEM<sup>+</sup> alone or supplemented with DOX (0.3 μg/ml), as well as both DOX and <i>Aloe vera</i> (5%, 10%, 25%, or 50%). After culture, ovaries were fixed for histological analysis (follicle morphology, growth and activation, extracellular matrix (ECM) configuration and stromal cell density), immunohistochemistry (<i>TNF-α</i> expression) or stored at - 80°C to evaluate the levels of mRNA for superoxide dismutase (<i>SOD</i>), catalase (<i>CAT</i>), nuclear factor-erythroid 2-related factor 2 (<i>NRF2</i>) and tumoral necrosis factor-α (<i>TNF-α</i>) by real-time PCR. The results showed that ovaries cultured with DOX had a lower percentage of normal follicles and reduced stromal cell density, but when <i>Aloe vera</i> extract was added to the culture medium, there was a protective effect on the ovarian structure against the deleterious effects of DOX. In addition, ovaries cultured with both DOX and <i>Aloe vera</i> (10 and 25%) had reduced <i>TNF-α</i> immunostaining and increased expression of mRNA for antioxidant enzymes (<i>SOD</i>, <i>CAT</i>, and <i>NRF2</i>). In conclusion, <i>Aloe vera</i> is associated with a protective effect on ovarian follicles and stromal cells against DOX-induced toxicity. Therefore, <i>Aloe vera</i> has great potential to preserve fertility in patients undergoing chemotherapy treatment, which often cause irreversible damage to oocytes.</p>\",\"PeriodicalId\":8970,\"journal\":{\"name\":\"Biotechnic & Histochemistry\",\"volume\":\" \",\"pages\":\"381-392\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biotechnic & Histochemistry\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1080/10520295.2025.2537829\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/4 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnic & Histochemistry","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1080/10520295.2025.2537829","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/4 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Protective in vitro effects of Aloe vera on doxorubicin-induced ovarian toxicity in mice.
The present study investigated the protective effect of Aloe vera extract against the toxic effects of doxorubicin (DOX) on mice ovaries cultured in vitro. Female Swiss mice with regular estrous cycle were used. The animals (n = 48) had their ovaries collected and cultured individually in a 24-well plate at 37.5°C in 5% CO2 for 6 days. The ovaries were culture DMEM+ alone or supplemented with DOX (0.3 μg/ml), as well as both DOX and Aloe vera (5%, 10%, 25%, or 50%). After culture, ovaries were fixed for histological analysis (follicle morphology, growth and activation, extracellular matrix (ECM) configuration and stromal cell density), immunohistochemistry (TNF-α expression) or stored at - 80°C to evaluate the levels of mRNA for superoxide dismutase (SOD), catalase (CAT), nuclear factor-erythroid 2-related factor 2 (NRF2) and tumoral necrosis factor-α (TNF-α) by real-time PCR. The results showed that ovaries cultured with DOX had a lower percentage of normal follicles and reduced stromal cell density, but when Aloe vera extract was added to the culture medium, there was a protective effect on the ovarian structure against the deleterious effects of DOX. In addition, ovaries cultured with both DOX and Aloe vera (10 and 25%) had reduced TNF-α immunostaining and increased expression of mRNA for antioxidant enzymes (SOD, CAT, and NRF2). In conclusion, Aloe vera is associated with a protective effect on ovarian follicles and stromal cells against DOX-induced toxicity. Therefore, Aloe vera has great potential to preserve fertility in patients undergoing chemotherapy treatment, which often cause irreversible damage to oocytes.
期刊介绍:
Biotechnic & Histochemistry (formerly Stain technology) is the
official publication of the Biological Stain Commission. The journal has been in continuous publication since 1926.
Biotechnic & Histochemistry is an interdisciplinary journal that embraces all aspects of techniques for visualizing biological processes and entities in cells, tissues and organisms; papers that describe experimental work that employs such investigative methods are appropriate for publication as well.
Papers concerning topics as diverse as applications of histochemistry, immunohistochemistry, in situ hybridization, cytochemical probes, autoradiography, light and electron microscopy, tissue culture, in vivo and in vitro studies, image analysis, cytogenetics, automation or computerization of investigative procedures and other investigative approaches are appropriate for publication regardless of their length. Letters to the Editor and review articles concerning topics of special and current interest also are welcome.