Literature DB >> 9951615

Does growth hormone prevent or accelerate aging?

A Bartke1, H M Brown-Borg, A M Bode, J Carlson, W S Hunter, R T Bronson.   

Abstract

It is very well documented that plasma growth hormone (GH) levels decline with age in the human and in experimental animals, and there is considerable evidence that age-related changes in body composition may be caused by reduced function of the GH-IGF-I system. However, excessive GH levels are associated with reduced life expectancy in acromegalic patients and with symptoms of accelerated aging in GH transgenic mice. Hereditary dwarf mice deficient in GH, prolactin, and TSH live much longer than their normal siblings. Possible mechanisms of delayed aging in dwarf mice include lower core body temperature and reduced oxidative processes. It is suggested that the controversies concerning the apparent potential of GH to both prevent and accelerate aging may be reconciled by interpreting the results in light of the negative relationship between body size and life span within a species.

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Year:  1998        PMID: 9951615     DOI: 10.1016/s0531-5565(98)00032-1

Source DB:  PubMed          Journal:  Exp Gerontol        ISSN: 0531-5565            Impact factor:   4.032


  26 in total

Review 1.  Hormonal regulation of longevity in mammals.

Authors:  Holly M Brown-Borg
Journal:  Ageing Res Rev       Date:  2007-02-20       Impact factor: 10.895

Review 2.  Role of the GH/IGF-1 axis in lifespan and healthspan: lessons from animal models.

Authors:  Darlene E Berryman; Jens Sandahl Christiansen; Gudmundur Johannsson; Michael O Thorner; John J Kopchick
Journal:  Growth Horm IGF Res       Date:  2008-08-16       Impact factor: 2.372

3.  Studies of aging in ames dwarf mice: Effects of caloric restriction.

Authors:  J A Mattison; C Wright; R T Bronson; G S Roth; D K Ingram; A Bartke
Journal:  J Am Aging Assoc       Date:  2000-01

4.  The nature and mechanism of superoxide production by the electron transport chain: Its relevance to aging.

Authors:  F Muller
Journal:  J Am Aging Assoc       Date:  2000-10

5.  Growth Hormone Receptor Antagonist Transgenic Mice Have Increased Subcutaneous Adipose Tissue Mass, Altered Glucose Homeostasis and No Change in White Adipose Tissue Cellular Senescence.

Authors:  Ross Comisford; Ellen R Lubbers; Lara A Householder; Ozan Suer; Tamara Tchkonia; James L Kirkland; Edward O List; John J Kopchick; Darlene E Berryman
Journal:  Gerontology       Date:  2015-09-16       Impact factor: 5.140

6.  A novel ENU-induced mutation, peewee, causes dwarfism in the mouse.

Authors:  Bokryeon Lee; Lee Bokryeon; Kiyoshi Kano; Jay Young; Simon W M John; Patsy M Nishina; Jurgen K Naggert; Kunihiko Naito
Journal:  Mamm Genome       Date:  2009-06-10       Impact factor: 2.957

7.  Patterns of metabolic activity during aging of the wild type and longevity mutants of Caenorhabditis elegans.

Authors:  B P Braeckman; K Houthoofd; J R Vanfleteren
Journal:  J Am Aging Assoc       Date:  2000-04

8.  Growth hormone and aging.

Authors:  A Bartke; H Brown-Borg; B Kinney; J Mattison; C Wright; S Hauck; K Coschigano; J Kopchick
Journal:  J Am Aging Assoc       Date:  2000-10

9.  Mitochondrial oxidant generation and oxidative damage in Ames dwarf and GH transgenic mice.

Authors:  H Brown-Borg; W T Johnson; S Rakoczy; M Romanick
Journal:  J Am Aging Assoc       Date:  2001-07

10.  Oxidative stress in hypopituitary dwarf mice and in transgenic mice overexpressing human and bovine GH.

Authors:  J C Carlson; R Bharadwaj; A Bartke
Journal:  Age (Omaha)       Date:  1999-10
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