Earticle

현재 위치 Home

Molecular Analysis of Growth Factor and Clock Gene Expression in the Livers of Rats with Streptozotocin-Induced Diabetes

첫 페이지 보기
  • 발행기관
    한국동물생명공학회(구 한국동물번식학회) 바로가기
  • 간행물
    Reproductive & developmental biology 바로가기
  • 통권
    Volume 33 No 3 (2009.09)바로가기
  • 페이지
    pp.163-169
  • 저자
    Joo-Heon Kim, Cheol-Soo Shim, Jinyoung Won, Youngji Park, Sookyoung Park, Jae Seon Kang, Yonggeun Hong
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A111951

※ 기관로그인 시 무료 이용이 가능합니다.

4,000원

원문정보

초록

영어
Many biological systems are regulated by an intricate set of feedback loops that oscillate with a circadian rhythm of roughly 24 h. This circadian clock mediates an increase in body temperature, heart rate, blood pressure, and cortisol secretion early in the day. Recent studies have shown changes in the amplitude of the circadian clock in the hearts and livers of streptozotocin (STZ)-treated rats. It is therefore important to examine the relationships between circadian clock genes and growth factors and their effects on diabetic phenomena in animal models as well as in human patients. In this study, we sought to determine whether diurnal variation in organ development and the regulation of metabolism, including growth and development during the juvenile period in rats, exists as a mechanism for anticipating and responding to the environment. Also, we examined the relationship between changes in growth factor expression in the liver and clock-controlled protein synthesis and turnover, which are important in cellular growth. Specifically, we assessed the expression patterns of several clock genes, including Per1, Per2, Clock, Bmal1, Cry1 and Cry2 and growth factors such as insulin-like growth factor (IGF)-1 and -2 and transforming growth factor (TGF)-β1 in rats with STZ-induced diabetes. Growth factor and clock gene expression in the liver at 1 week post-induction was clearly increased compared to the level in control rats. In contrast, the expression patterns of the genes were similar to those observed after 5 weeks in the STZ-treated rats. The increase in gene expression is likely a compensatory change in response to the obstruction of insulin function during the initial phase of induction. However, as the period of induction was extended, the expression of the compensatory genes decreased to the control level. This is likely the result of decreased insulin secretion due to the destruction of beta cells in the pancreas by STZ.

목차

ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
  Animals and Induction of Diabetes
  Experimental Design
  RNA Extraction and RT-PCR
  Statistical Analysis
 RESULTS
  Blood Glucose Levels
  Growth Factor Gene Expression
 DISCUSSION
 REFERENCES

키워드

Diabetes Growth factor Clock gene Circadian rhythm Streptozotocin

저자

  • Joo-Heon Kim [ Institute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University ]
  • Cheol-Soo Shim [ Institute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University ]
  • Jinyoung Won [ Department of Physical Therapy, College of Biomedical Science & Engineering, Inje University ]
  • Youngji Park [ Department of Physical Therapy, College of Biomedical Science & Engineering, Inje University ]
  • Sookyoung Park [ Department of Physical Therapy, College of Biomedical Science & Engineering, Inje University ]
  • Jae Seon Kang [ Department of Pharmacy, Kyungsung University ]
  • Yonggeun Hong [ Department of Physical Therapy, College of Biomedical Science & Engineering, Inje University ] 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
    Reproductive & developmental biology
  • 간기
    계간
  • pISSN
    1738-2432
  • eISSN
    2288-0151
  • 수록기간
    1977~2018
  • 십진분류
    KDC 527 DDC 636

이 권호 내 다른 논문 / Reproductive & developmental biology Volume 33 No 3

    피인용수 : 0(자료제공 : 네이버학술정보)

    함께 이용한 논문 이 논문을 다운로드한 분들이 이용한 다른 논문입니다.

      페이지 저장