Wednesday 6 November 2013

What is human growth hormone?


Growth Hormones and Disease Symptoms

The pituitary (hypophysis) is an acorn-sized gland located at the base of the brain that makes important hormones and disseminates stored hypothalamic hormones. The hypothalamus controls the activity of the pituitary gland by sending signals along a network of blood vessels and nerves that connects them. The main portion of the pituitary gland, the adenohypophysis, makes six trophic hormones that control many body processes by causing other endocrine glands to produce hormones. The neurohypophysis, the remainder of the pituitary, stores two hypothalamic hormones for dissemination.













Dwarfism
is caused by the inability to produce growth hormone. When humans lack only human growth hormone (HGH), resultant dwarfs have normal to superior intelligence. However, if the pituitary gland is surgically removed (hypophysectomy), the absence of other pituitary hormones causes additional mental and gender problems. The symptoms of dwarfism are inability to grow at a normal rate or attain adult size. Many dwarfs are two to three feet tall. In contrast, some giants have reached heights of more than eight feet. The advent of gigantism
often begins with babies born with pituitary tumors that cause the production of too much HGH, resulting in continued excess growth. People who begin oversecreting HGH as adults (also caused by tumors) do not grow taller. However, the bones in their feet, hands, skull, and brow ridges overgrow, causing disfigurement and pain, a condition known as acromegaly.


Dwarfism that is uncomplicated by the absence of other pituitary hormones is treated with growth hormone injections. Humans undergoing such therapy can be treated with growth hormones from humans or primates. Growth hormone from all species is a protein made of approximately two hundred amino acids strung into a chain of complex shape. However, differences in amino acids and chain arrangement in different species cause shape differences; therefore, growth hormone used for treatment must be extracted from a related species. Treatment for acromegaly and gigantism involves the removal of the tumor. In cases where it is necessary to remove the entire pituitary gland, other hormones must be given in addition to HGH. Their replacement is relatively simple. Such hormones usually come from animals. For many years, the sole source of HGH was pituitaries donated to science. This provided the ability to treat fewer than one thousand individuals per year. Molecular genetics has solved that problem by devising the means to manufacture large amounts of transgenic HGH.




Growth Hormone Operation and Genetics

In the mid-1940s, growth hormone was isolated and used to explain why pituitary extracts increase growth. One process associated with HGH action involves cartilage cells at the ends of long bones (such as those in arms and legs). HGH injection causes these epiphysial plate cells (EPCs) to rapidly reproduce and stack up. The EPCs then die and leave a layer of protein, which becomes bone. From this it has been concluded that growth hormone acts to cause all body bones to grow until adult size is reached. It is unclear why animals and humans from one family exhibit adult size variation. The differences are thought to be genetic and related to production and cooperation of HGH, other hormones, and growth factors.


Genetic research has produced transgenic HGH in bacteria through the use of genetic engineering technology. The gene that codes for HGH is spliced into a special circular piece of DNA called a plasmid expression vector, thus producing a recombinant expression vector. This recombinant vector is then put into bacterial cells, where the bacteria express the HGH gene. These transgenic bacteria can then be grown on an industrial scale. After bacterial growth ends, a huge number of cells are harvested and HGH is isolated. This method enables isolation of enough HGH to treat anyone who needs it.




Impact and Applications

One use of transgenic HGH is the treatment of acromegaly, dwarfism, and gigantism. The availability of large quantities of HGH has also led to other biomedical advances in growth and endocrinology. For example, growth hormone does not affect EPCs in tissue culture. Ensuing research, first with animal growth hormone and later with HGH, uncovered the EPC stimulant somatomedin. Somatomedin stimulates growth in other tissues as well and belongs to a protein group called insulin-like growth factors. Many researchers have concluded that the small size of women compared to men is caused by estrogen-diminished somatomedin action on EPCs. Estrogen, however, stimulates female reproductive system growth by interacting with other insulin-like growth factors.


Another interesting experiment involving HGH and genetic engineering is the production of rat-sized mice. This venture, accomplished by putting the HGH gene into a mouse chromosome, has important implications for understanding such mysteries as the basis for species specificity of growth hormones and maximum size control for all organisms. Hence, experiments with HGH and advancements in genetic engineering technology have led to, and should continue to lead to, valuable insights into the study of growth and other aspects of life science.




Key terms




endocrine gland


:

a gland that secretes hormones into the circulatory system




hypophysectomy

:

surgical removal of the pituitary gland





pituitary gland


:

an endocrine gland located at the base of the brain; also called the hypophysis




transgenic protein

:

a protein produced by an organism using a gene that was derived from another organism





Bibliography


“Can We Prevent Aging? Tips from the National Institute on Aging.” National Institute on Aging. US Department of Health and Human Services, June 2010. Web. 4 Aug. 2014.



Cohen, Susan, and Christine Cosgrove. Normal at Any Cost: Tall Girls, Short Boys, and the Medical Industry’s Quest to Manipulate Height. New York: Tarcher, 2009. Print.



Eiholzer, Urs. Prader-Willi Syndrome: Effects of Human Growth Hormone Treatment. New York: Karger, 2001. Print.



Flyvbjerg, Allan, Hans Orskov, and George Alberti, eds. Growth Hormone and Insulin-Like Growth Factor I in Human and Experimental Diabetes. New York: Wiley, 1993. Print.



Ho, Ken. Growth Hormone Related Diseases and Therapy: A Molecular and Physiological Perspective for the Clinician. New York: Humana, 2011. Print.



Jorgensen, Jens Otto Lunde, and Jens Sandahl Christiansen, eds. Growth Hormone Deficiency in Adults. New York: Karger, 2005. Print.



Shiverick, Kathleen T., and Arlan L. Rosenbloom, eds. Human Growth Hormone Pharmacology: Basic and Clinical Aspects. Boca Raton: CRC, 1995. Print.



Smith, Roy G., and Michael O. Thorner, eds. Human Growth Hormone: Research and Clinical Practice. Totowa: Humana, 2000. Print.



Ulijaszek, J. S., M. Preece, and S. J. Ulijaszek. The Cambridge Encyclopedia of Human Growth and Development Growth Standards. New York: Cambridge UP, 1998. Print.



Williams, Mary E. Growth Disorders. Farmington Hills: Greenhaven, 2012. Print.

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