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Original Article

Aflatoxin B1-induced oxidative stress in canine small intestinal cells

첫 페이지 보기
  • 발행기관
    한국동물생명공학회(구 한국동물번식학회) 바로가기
  • 간행물
    Journal of Animal Reproduction and Biotechnology 바로가기
  • 통권
    Volume. 39 No. 2 (2024.06)바로가기
  • 페이지
    pp.105-113
  • 저자
    Hyun-Woo Cho, Kangmin Seo, Min Young Lee, Sang-Yeob Lee, Kyoung Min So, Ki Hyun Kim, Ju Lan Chun
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A452084

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원문정보

초록

영어
Background: Aflatoxin B1 (AFB1) is a toxic metabolite generated by Aspergillus species and is commonly detected during the processing and storage of food; it is considered a group I carcinogen. The hepatotoxic effects, diseases, and mechanisms induced by AFB1 owing to chronic or acute exposure are well documented; however, there is a lack of research on its effects on the intestine, which is a crucial organ in the digestive process. Dogs are often susceptible to chronic AFB1 exposure owing to lack of variation in their diet, unlike humans, thereby rendering them prone to its effects. Therefore, we investigated the effects of AFB1 on canine small intestinal epithelial primary cells (CSIc). Methods: We treated CSIc with various concentrations of AFB1 (0, 1.25, 2.5, 5, 10, 20, 40, and 80 μM) for 24 h and analyzed cell viability and transepithelial-transendothelial electrical resistance (TEER) value. Additionally, we analyzed the mRNA expression of tight junction-related genes (OCLN, CLDN3, TJP1, and MUC2), antioxidant-related genes (CAT and GPX1), and apoptosis-related genes (BCL2, Bax, and TP53). Results: We found a significant decrease in CSIc viability and TEER values after treatment with AFB1 at concentrations of 20 μM or higher. Quantitative polymerase chain reaction analysis indicated a downregulation of OCLN, CLDN3, and TJP1 in CSIc treated with 20 μM or higher concentrations of AFB1. Additionally, AFB1 treatment downregulated CAT , GPX1, and BCL2. Conclusions: Acute exposure of CSIc to AFB1 induces toxicity, and exposure to AFB1 above a certain threshold compromises the barrier integrity of CSIc.

목차

ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
Cell culture
Cell viability assay
Transepithelial-transendothelial electrical resistance assay
RNA extraction and quantitative reverse transcription-polymerasechain reaction (qPCR)
Statistical analysis
RESULTS
Aflatoxin B1 decreased the viability of CSIc and impaired barrier integrity
AFB1 downregulated antioxidant and apoptosisrelated genes
DISCUSSION
CONCLUSION
REFERENCES

저자

  • Hyun-Woo Cho [ National Institute of Animal Science, Rural Development Administration, Wanju 55365, Korea ]
  • Kangmin Seo [ National Institute of Animal Science, Rural Development Administration, Wanju 55365, Korea ]
  • Min Young Lee [ National Institute of Animal Science, Rural Development Administration, Wanju 55365, Korea ]
  • Sang-Yeob Lee [ National Institute of Animal Science, Rural Development Administration, Wanju 55365, Korea ]
  • Kyoung Min So [ National Institute of Animal Science, Rural Development Administration, Wanju 55365, Korea ]
  • Ki Hyun Kim [ National Institute of Animal Science, Rural Development Administration, Wanju 55365, Korea ]
  • Ju Lan Chun [ National Institute of Animal Science, Rural Development Administration, Wanju 55365, Korea ] Corresponding Author

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국동물생명공학회(구 한국동물번식학회) [The Korean Society of Animal Reproduction and Biotechnology]
  • 설립연도
    1976
  • 분야
    농수해양>축산학
  • 소개
    동물번식생리학, 동물생명공학, 수의학, 인공수정 및 수정란이식을 이용한 동물개량에 관한 이론과 기술의 발전을 통해 학계, 연구계, 산업계 및 양축가 상호간의 협력을 도모함으로써 동물과학발전 및 사회일반의 이익에 기여 한다는 목적을 위해 노력해 나가겠습니다.

간행물

  • 간행물명
    Journal of Animal Reproduction and Biotechnology
  • 간기
    계간
  • pISSN
    2671-4639
  • eISSN
    2671-4663
  • 수록기간
    2019~2026
  • 십진분류
    KDC 527 DDC 636

이 권호 내 다른 논문 / Journal of Animal Reproduction and Biotechnology Volume. 39 No. 2

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