HIGH-FAT DIET WITH STRESS IMPAIRED ISLETS' INSULIN SECRETION BY REDUCING PLASMA ESTRADIOL AND PANCREATIC GLUT2 PROTEIN LEVELS IN RATS' PROESTRUS PHASE

被引:0
|
作者
Salimi, M. [1 ]
Zardooz, H. [2 ,3 ,4 ]
Khodagholi, F. [5 ,6 ]
Rostamkhani, F. [7 ]
Shaerzadeh, F. [8 ]
机构
[1] Shahid Beheshti Univ Med Sci, Sch Med, Dept Physiol, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Sch Med, Neurophysiol Res Ctr, POB 19615-1178, Tehran, Iran
[3] Shahid Beheshti Univ Med Sci, Sch Med, Dept Physiol, POB 19615-1178, Tehran, Iran
[4] Shahid Beheshti Univ Med Sci, Res Inst Endocrine Sci, Endocrine Physiol Res Ctr, Tehran, Iran
[5] Shahid Beheshti Univ Med Sci, NeuroBiol Res Ctr, Tehran, Iran
[6] Shahid Beheshti Univ Med Sci, Neurosci Res Ctr, Tehran, Iran
[7] Islamic Azad Univ, Yadegar E Imam Khomeini RAH Branch, Coll Basic Sci, Dept Biol, Tehran, Iran
[8] Hormozgan Univ Med Sci, Dept Physiol, Bandar Abbas, Iran
来源
JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY | 2016年 / 67卷 / 05期
关键词
high-fat diet; stress; estrous cycle; insulin secretion; isolated islets; ESTROUS-CYCLE; GLUCOSE-TOLERANCE; LEPTIN RECEPTOR; SEX-DIFFERENCES; ENERGY-BALANCE; CORPUS-LUTEUM; FEMALE RATS; BETA-CELLS; IN-VITRO; MOUSE;
D O I
暂无
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
This study was conducted to determine whether two estrus phases (proestrus and diestrus) in female rats may influence the metabolic response to a high-fat diet and/or stress, focusing on pancreatic insulin secretion and content Animals were divided into high-fat and normal diet groups, then each group was subdivided into stress and non-stress groups, and finally, each one of these was divided into proestrus and diestrus subgroups. At the end of high-fat diet treatment, foot-shock stress was applied to the animals. Then, blood samples were taken to measure plasma factors. Finally, the pancreas was removed for determination of glucose transporter 2 (GLUT2) protein levels and assessment of insulin content and secretion of the isolated islets. In the normal and high-fat diet groups, stress increased plasma corticosterone concentration in both phases. In both study phases, high-fat diet consumption decreased estradiol and increased leptin plasma levels. In the high-fat diet group in response to high glucose concentration, a reduction in insulin secretion was observed in the proestrus phase compared with the same phase in the normal diet group in the presence and absence of stress. Also, high-fat diet decreased the insulin content of islets in the proestrus phase compared with the normal diet. High-fat diet and/or stress caused a reduction in islet GLUT2 protein levels in both phases. In conclusion, it seems possible that high-fat diet alone or combined with foot-shock, predispose female rats to impaired insulin secretion, at least in part, by interfering with estradiol levels in the proestrus phase and decreasing pancreatic GLUT2 protein levels.
引用
收藏
页码:653 / 666
页数:14
相关论文
共 41 条
  • [1] Pancreatic GLUT2 protein expression and isolated islets insulin secretion decreased in high-fat fed rat dams
    Karbaschi, Roxana
    Zardooz, Homeira
    JOURNAL OF DIABETES AND METABOLIC DISORDERS, 2023, 22 (02) : 1511 - 1518
  • [2] Pancreatic GLUT2 protein expression and isolated islets insulin secretion decreased in high-fat fed rat dams
    Roxana Karbaschi
    Homeira Zardooz
    Journal of Diabetes & Metabolic Disorders, 2023, 22 : 1511 - 1518
  • [3] EFFECT OF HIGH-FAT DIET ON THE GENE-EXPRESSION OF PANCREATIC GLUT2 AND GLUCOKINASE IN RATS
    KIM, YB
    IWASHITA, S
    TAMURA, T
    TOKUYAMA, K
    SUZUKI, M
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 208 (03) : 1092 - 1098
  • [4] Endoplasmic reticulum stress inhibition ameliorated WFS1 expression alterations and reduced pancreatic islets' insulin secretion induced by high-fat diet in rats
    Binayi, Fateme
    Fahanik-Babaei, Javad
    Salimi, Mina
    Eskandari, Farzaneh
    Sahraei, Mohammad
    Ranjbary, Ali Ghorbani
    Ghasemi, Rasoul
    Hedayati, Mehdi
    Khodagholi, Fariba
    Eliassi, Afsaneh
    Zardooz, Homeira
    SCIENTIFIC REPORTS, 2023, 13 (01)
  • [5] Endoplasmic reticulum stress inhibition ameliorated WFS1 expression alterations and reduced pancreatic islets’ insulin secretion induced by high-fat diet in rats
    Fateme Binayi
    Javad Fahanik-Babaei
    Mina Salimi
    Farzaneh Eskandari
    Mohammad Sahraei
    Ali Ghorbani Ranjbary
    Rasoul Ghasemi
    Mehdi Hedayati
    Fariba Khodagholi
    Afsaneh Eliassi
    Homeira Zardooz
    Scientific Reports, 13
  • [6] Postnatal knockout of beta cell insulin receptor impaired insulin secretion in male mice exposed to high-fat diet stress
    Oakie, Amanda
    Zhou, Liangyi
    Rivers, Sydney
    Cheung, Christy
    Li, Jinming
    Wang, Rennian
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2020, 499
  • [7] EFFECTS OF A HIGH-FAT DIET AND ELECTRIC STRESS ON INSULIN-RESPONSE TO HYDROCORTISONE AND CATECHOLAMINES IN ISOLATED PANCREATIC-ISLETS
    YAMAGUCHI, K
    MATSUOKA, A
    HORMONE AND METABOLIC RESEARCH, 1981, 13 (01) : 9 - 13
  • [8] Ablation of Elovl6 protects pancreatic islets from high-fat diet-induced impairment of insulin secretion
    Tang, Nie
    Matsuzaka, Takashi
    Suzuki, Marii
    Nakano, Yuta
    Zao, Hui
    Yokoo, Tomotaka
    Suzuki-Kemuriyama, Noriko
    Kuba, Motoko
    Okajima, Yuka
    Takeuchi, Yoshinori
    Kobayashi, Kazuto
    Iwasaki, Hitoshi
    Yatoh, Shigeru
    Takahashi, Akimitsu
    Suzuki, Hiroaki
    Sone, Hirohito
    Shimada, Masako
    Nakagawa, Yoshimi
    Yahagi, Naoya
    Yamada, Nobuhiro
    Shimano, Hitoshi
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2014, 450 (01) : 318 - 323
  • [9] REDUCED LEVELS OF MESSENGER-RNA FOR CALCIUM CHANNELS, GLUT2 AND GLUCOKINASE ARE ASSOCIATED WITH IMPAIRED INSULIN-SECRETION IN FASTED RATS
    IWASHIMA, Y
    KONDO, A
    ETO, M
    SEINO, S
    MAKINO, I
    DIABETES, 1994, 43 : A183 - A183
  • [10] Impaired glucose-stimulated insulin secretion and increased triglyceride content of the islets in heterozygous PPARγ deficient mice on the high-fat diet
    Matsui, J
    Terauchi, Y
    Eto, K
    Yamauchi, T
    Kubota, N
    Noda, M
    Komeda, K
    Kadowaki, T
    DIABETES, 2002, 51 : A13 - A13