Effects of dietary restriction on the expression of insulin-signaling-related genes in long-lived mutant mice.

Hypopituitary Ames dwarf mice and growth-hormone-resistant (growth hormone receptor knockout, GHRKO) mice have reduced plasma levels of insulin-like growth factor 1 and insulin, enhanced insulin sensitivity and a remarkably increased life span. This resembles the phenotypic characteristics of genetically normal animals subjected to dietary restriction (DR). Interestingly, DR leads to further increases in insulin sensitivity and longevity in Ames dwarfs but not in GHRKO mice. It was therefore of interest to examine the effects of DR on the expression of insulin-related genes in these two types of long-lived mutant mice. The effects of DR partially overlapped but did not duplicate the effects of Ames dwarfism or GHR deletion on the expression of genes related to insulin signaling and cell responsiveness to insulin. Moreover, the effects of DR on the expression of the examined genes in different insulin target organs were not identical. Some of the insulin-related genes were similarly affected by DR in both GHRKO and normal mice, some were affected only in GHRKO mice and some only in normal animals. This last category is of particular interest since genes affected in normal but not GHRKO mice may be related to mechanisms by which DR extends longevity.

[1]  Andrzej Bartke,et al.  Targeted disruption of growth hormone receptor interferes with the beneficial actions of calorie restriction , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[2]  A. Bartke Printed in U.S.A. Copyright © 2005 by The Endocrine Society doi: 10.1210/en.2005-0411 Minireview: Role of the Growth Hormone/Insulin-Like Growth Factor System in Mammalian Aging , 2022 .

[3]  A. Bartke,et al.  Effects of caloric restriction on insulin pathway gene expression in the skeletal muscle and liver of normal and long-lived GHR-KO mice , 2005, Experimental Gerontology.

[4]  A. Bartke,et al.  Local expression of GH and IGF-1 in the hippocampus of GH-deficient long-lived mice , 2005, Neurobiology of Aging.

[5]  A. Bartke,et al.  Effect of every other day feeding diet on gene expression in normal and in long-lived Ames dwarf mice , 2005, Experimental Gerontology.

[6]  C. Kenyon The Plasticity of Aging: Insights from Long-Lived Mutants , 2005, Cell.

[7]  M. Lipsett,et al.  Disruption of growth hormone receptor gene causes diminished pancreatic islet size and increased insulin sensitivity in mice. , 2004, American journal of physiology. Endocrinology and metabolism.

[8]  A. Bartke,et al.  Divergent effects of caloric restriction on gene expression in normal and long-lived mice. , 2004, The journals of gerontology. Series A, Biological sciences and medical sciences.

[9]  F. Dominici,et al.  The Role of Growth Hormone Signaling in the Control of Ageing , 2004 .

[10]  Amy N Holland,et al.  Deletion, but not antagonism, of the mouse growth hormone receptor results in severely decreased body weights, insulin, and insulin-like growth factor I levels and increased life span. , 2003, Endocrinology.

[11]  M. Tatar,et al.  The Endocrine Regulation of Aging by Insulin-like Signals , 2003, Science.

[12]  C. Finch,et al.  Evolutionary Medicine: From Dwarf Model Systems to Healthy Centenarians? , 2003, Science.

[13]  Matthias Blüher,et al.  Extended Longevity in Mice Lacking the Insulin Receptor in Adipose Tissue , 2003, Science.

[14]  Martin Holzenberger,et al.  IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice , 2003, Nature.

[15]  A. Galecki,et al.  Gene expression patterns in calorically restricted mice: partial overlap with long-lived mutant mice. , 2002, Molecular endocrinology.

[16]  A. Galecki,et al.  Big mice die young: early life body weight predicts longevity in genetically heterogeneous mice , 2002, Aging cell.

[17]  A. Bartke,et al.  Consequences of growth hormone (GH) overexpression and GH resistance , 2002, Neuropeptides.

[18]  F. Dominici,et al.  Increased insulin sensitivity and upregulation of insulin receptor, insulin receptor substrate (IRS)-1 and IRS-2 in liver of Ames dwarf mice. , 2002, The Journal of endocrinology.

[19]  H. Brown-Borg,et al.  Mitochondrial oxidant generation and oxidative damage in Ames dwarf and GH transgenic mice , 2001, Journal of the American Aging Association.

[20]  A. Bartke,et al.  Reduced Levels of Thyroid Hormones, Insulin, and Glucose, and Lower Body Core Temperature in the Growth Hormone Receptor/Binding Protein Knockout Mouse , 2001, Experimental biology and medicine.

[21]  Richard A. Miller,et al.  Lifespan extension and delayed immune and collagen aging in mutant mice with defects in growth hormone production , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[22]  E. Hafen,et al.  Extension of Life-Span by Loss of CHICO, a Drosophila Insulin Receptor Substrate Protein , 2001, Science.

[23]  J. Terwilliger,et al.  Roles of growth hormone and insulin-like growth factor 1 in mouse postnatal growth. , 2001, Developmental biology.

[24]  D. Clemmons,et al.  Assessment of growth parameters and life span of GHR/BP gene-disrupted mice. , 2000, Endocrinology.

[25]  H. Brown-Borg,et al.  Catalase expression in delayed and premature aging mouse models☆ , 2000, Experimental Gerontology.

[26]  A. Bartke Delayed aging in Ames dwarf mice. Relationships to endocrine function and body size. , 2000, Results and problems in cell differentiation.

[27]  S. Bennett,et al.  Pleiotropic effects of growth hormone and insulin-like growth factor (IGF)-1 on biological aging: inferences from moderate caloric-restricted animals. , 1999, The journals of gerontology. Series A, Biological sciences and medical sciences.

[28]  A. Bartke,et al.  Low Body Temperature in Long-Lived Ames Dwarf Mice at Rest and During Stress , 1999, Physiology & Behavior.

[29]  A. Bartke,et al.  Deficits in female reproductive function in GH-R-KO mice; role of IGF-I. , 1999, Endocrinology.

[30]  A. Bartke,et al.  Pituitary and testicular function in growth hormone receptor gene knockout mice. , 1999, Endocrinology.

[31]  T. Wagner,et al.  A mammalian model for Laron syndrome produced by targeted disruption of the mouse growth hormone receptor/binding protein gene (the Laron mouse). , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[32]  Koutarou D. Kimura,et al.  daf-2, an insulin receptor-like gene that regulates longevity and diapause in Caenorhabditis elegans. , 1997, Science.

[33]  R. Miskin,et al.  Transgenic mice overexpressing urokinase-type plasminogen activator in the brain exhibit reduced food consumption, body weight and size, and increased longevity. , 1997, The journals of gerontology. Series A, Biological sciences and medical sciences.

[34]  Wei Wu,et al.  Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism , 1996, Nature.

[35]  Andrzej Bartke,et al.  Dwarf mice and the ageing process , 1996, Nature.

[36]  M. Rosenfeld,et al.  The Ames dwarf gene is required for Pit-1 gene activation. , 1995, Developmental biology.

[37]  A. Bartke,et al.  Assessment of the Primary Adrenal Cortical and Pancreatic Hormone Basal Levels in Relation to Plasma Glucose and Age in the Unstressed Ames Dwarf Mouse , 1995, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[38]  A. Bartke INFLUENCE OF LUTEOTROPHIN ON FERTILITY OF DWARF MICE. , 1965, Journal of reproduction and fertility.

[39]  A. Bartke,et al.  Histology of the anterior hypophysis, thyroid and gonads of two types of dwarf mice , 1964, The Anatomical record.