Adipose derived hormones

Share on Facebook Share on Twitter Email
Wikipedia on Answers.com:

Adipose derived hormones

Top

Adipose tissue is an important endocrine organ that secretes numerous protein hormones, including leptin, adiponectin, and resistin. These hormones generally influence energy metabolism, which is of great interest to the understanding and treatment of type 2 diabetes and obesity.

Their relative roles in modifying appetite, insulin resistance and atherosclerosis are the subjects of intense research, as they may be modifiable causes of morbidity in people with obesity.[1][2]

History of adipose derived hormones

It had been shown that adipose tissue secreted some unknown factor that influenced appetite. However, the importance of adipose tissue as an endocrine organ was only fully appreciated in 1995 with the discovery of Leptin, the protein product of the Ob gene.[3][4][5] Leptin is a strong appetite suppressant that, when deleted, causes early onset severe obesity in humans and in animal models. The discovery of leptin and its effects on appetite led to hopes of a treatment for obesity and type 2 diabetes, a major disease in the developed world. Unfortunately, clinical studies using leptin as a treatment for obesity in humans failed to show improvement, leading some scientists to conclude that the brain can become resistant to leptin, even at supra-physiological levels (the so-called "ceiling effect"), rendering treatment with leptin ineffective. However, as geneticists learn more from the few cases of leptin gene mutations, the possibility remains that, although leptin was ineffective at treating obesity across the population, some individual obese patients might still benefit from its use as an anti-obesity medication.[6]

Research into the adipose-derived hormones adiponectin and resistin is ongoing. Like leptin, these hormones also affect energy balance and metabolism, and are therefore targets for new drug research.

References

  1. ^ Matsuzawa Y, Funahashi T, Nakamura T (November 1999). "Molecular mechanism of metabolic syndrome X: contribution of adipocytokines adipocyte-derived bioactive substances". Ann. N. Y. Acad. Sci. 892: 146–54. doi:10.1111/j.1749-6632.1999.tb07793.x. PMID 10842660. http://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0077-8923&date=1999&volume=892&spage=146. 
  2. ^ Funahashi T, Nakamura T, Shimomura I, et al. (February 1999). "Role of adipocytokines on the pathogenesis of atherosclerosis in visceral obesity". Intern. Med. 38 (2): 202–6. PMID 10225688. http://joi.jlc.jst.go.jp/JST.Journalarchive/internalmedicine1992/38.202?from=PubMed. 
  3. ^ Pelleymounter MA, Cullen MJ, Baker MB, et al. (July 1995). "Effects of the obese gene product on body weight regulation in ob/ob mice". Science 269 (5223): 540–3. doi:10.1126/science.7624776. PMID 7624776. http://www.sciencemag.org/cgi/pmidlookup?view=long&pmid=7624776. 
  4. ^ Halaas JL, Gajiwala KS, Maffei M, et al. (July 1995). "Weight-reducing effects of the plasma protein encoded by the obese gene". Science 269 (5223): 543–6. doi:10.1126/science.7624777. PMID 7624777. http://www.sciencemag.org/cgi/pmidlookup?view=long&pmid=7624777. 
  5. ^ Campfield LA, Smith FJ, Guisez Y, Devos R, Burn P (July 1995). "Recombinant mouse OB protein: evidence for a peripheral signal linking adiposity and central neural networks". Science 269 (5223): 546–9. doi:10.1126/science.7624778. PMID 7624778. http://www.sciencemag.org/cgi/pmidlookup?view=long&pmid=7624778. 
  6. ^ Fischer-Posovszky P, von Schnurbein J, Moepps B, et al. (June 2010). "A new missense mutation in the leptin gene causes mild obesity and hypogonadism without affecting T cell responsiveness". J. Clin. Endocrinol. Metab. 95 (6): 2836–40. doi:10.1210/jc.2009-2466. PMID 20382689. http://jcem.endojournals.org/cgi/pmidlookup?view=long&pmid=20382689. 

Post a question - any question - to the WikiAnswers community:

Copyrights: