Journals / International Archives of Medical Research / 2013 / Cilt: 5 - Sayı: 2

The Role of Growth Hormone in Regulation and Secretion of Ghrelin

Pages
1–8
Publication Date
2013-12-01
DOI
—
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

These data indicate that ghrelin is the main driving force behind the enhanced GH secretion during fasting.

📌 3 Key Takeaways

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Objective & Hypothesis:Background: Ghrelin is a novel growth hormone (GH) releaser acylated peptide that has recently been purified from stomach and potently binds to the GH secretagogue receptor.
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Key Findings & Data:Age-related decreases in energy expenditure have been associated with the loss of skeletal muscle and decline of food intake, possibly through a mechanism involving changes of GH secretion and feeding behavior.
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Conclusion & Impact:These data indicate that ghrelin is the main driving force behind the enhanced GH secretion during fasting.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Ghrelin · growth hormon · food intake

Abstract

Background: Ghrelin is a novel growth hormone (GH) releaser acylated peptide that has recently been purified from stomach and potently binds to the GH secretagogue receptor. In rats, fasting leads to elevated serum GH concentrations. Age-related decreases in energy expenditure have been associated with the loss of skeletal muscle and decline of food intake, possibly through a mechanism involving changes of GH secretion and feeding behavior. Ghrelin releases GH in vitro and in vivo in animal models, however its actions and specificity in humans are unknown. Method: We investigate the relationship between age-related changes of growth hormone secretion and/or food intake and ghrelin function. Ghrelin (10 nmol/kg body weight) was administered intravenously to male 3-, 12-, 24-and 27-month-old Wistar adult rats, after which growth hormone concentrations and 2 h food intake were measured. Results: Intravenous administration of ghrelin to rats increased food intake in all generations. In addition ghrelin administration elicited a marked increase in plasma GH levels, with the peak occurring 15 min after administration. Conclusion: These changes in serum ghrelin concentrations during fasting were followed by similar, profound changes in serum GH levels. These data indicate that ghrelin is the main driving force behind the enhanced GH secretion during fasting.

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Cite This Article

OBAY, B. D., BİLGİN, H. M., TAŞDEMİR, E., YILDIRIM, Y., ŞERMET, A., KOÇYİĞİT, Y. (2013). The Role of Growth Hormone in Regulation and Secretion of Ghrelin. International Archives of Medical Research, Cilt: 5 - Sayı: 2, 1–8. https://ajindex.com/articles/764817

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References (14)

  1. Kojima M, Hosoda H, Date Y, Nakazato M, Matsuo H and Kangawa K. (1999) Ghrelin is a novel growth hormone releasing acylated peptide from stomach. Nature, 402: 656-660.
  2. Date Y, Toshinai K, Koda S, et al. (2005) Peripheral interaction of ghrelin with cholecystokinin on feeding regulation. Endocrinology, 146: 3518-3525.
  3. Toshinai K, Yamaguchi H, Sun Y, et al. (2006) Des-acyl Ghrelin induces food intake by a mechanism independent of the growth hormone secretagogue receptor. Endocrinology, 147: 2306-2314. Sandstrom 0, Mahdavi J and El-Salhy M. (1999) Age-related changes in antral endocrine cells in mice. Histol Histopathol, 14: 31-36.
  4. Rigamonti AE, Pincelli AI, Corra B, et al. (2002) Plasma ghrelin concentrations in elderly subjects: comparison with anorexic and obese patients. J Endocrinol, 175: R1-R5. Broglio F, Benso A, Castiglioni C, et al. (2003) The endocrine response to ghrelin as a function of gender in humans in young and elderly subjects. J Clin Endocrinol Metab, 88: 1537-1542.
  5. Englander EW, Gomez GA and Greeley Jr GH. (2004) Alterations in stomach ghrelin production and in ghrelin- induced growth hormone secretion in the age rats. Meek Ageing Dev, 125: 871-875.
  6. Anawalt BD and Merriam GR. (2001) Neuroendocrine aging in men. Andropause and somatopause. Endocrinol Metab Clin North Am, 30: 647-649. Lamberts SWJ, van den Beld AW and van den Lely AJ. (1997) The endocrinology of aging. Science, 278: 419-424.
  7. Macintosh C, Moorley JE and Chapman IM. (2000) The anorexia of aging. Nutrition, 16: 983-995.
  8. Morley JE. (2001) Decreased food intake with aging. J Gerontol A Biol Sci Med Sci, 56: 81-88.Morley E. and Thomas DR. (1999) Anorexia and aging: pathophysiology. Nutrition, 15: 499-503.
  9. Morley JE. (2001) Anorexia, sarcopenia, and aging. Nutrition, 17: 660-663.
  10. Baumgartner RN, Koehler KM, Gallagher D, et al. (1998) Epidemiology of sarcopenia among the elderly in New Mexico. Am J Epidemiol, 147: 755-763.
  11. Sullivan DH. (1998) The role of nutrition in increased morbidity and mortality. Clin Geriatr Med, 11: 661-674.
  12. Asakawa A, Inui A, Kaga T, et al. (2001) Ghrelin is an appetite-stimulatory signal from stomach with structural resemblance to motilin. Gastroenterology, 120: 337-345.
  13. Lawrence CB, Snape AC, Baudoin FM and Luckman SM. (2002) Acute central ghrelin and GH secretagogues induce feeding and activate brain appetite centers. Endocrinology, 143: 155-162.
  14. Nakazato M, Murakami N, Date Y, et al. (2001) A role for ghrelin in the central regulation of feeding. Natur