MadSci Network: Medicine |
Hi Katie. First, read the following 2 articles. The source of the articles is mentioned at the end of each. Then try the links. ARTICLE 1 The adrenal medulla consists of masses of neurons that are part of the sympathetic branch of the autonomic nervous system. Instead of releasing their neurotransmitters at a synapse, these neurons release them into the blood. Thus, although part of the nervous system, the adrenal medulla functions as an endocrine gland. The adrenal medulla releases: adrenaline (also called epinephrine) and noradrenaline (also called norepinephrine) Both are derived from the amino acid tyrosine. Release of adrenaline and noradrenaline is triggered by nervous stimulation in response to physical or mental stress. The hormones bind to adrenergic receptors - transmembrane proteins in the plasma membrane of many cell types. Some of the effects are: increase in the rate and strength of the heartbeat resulting in increased blood pressure blood shunted from the skin and viscera to the skeletal muscles, coronary arteries, liver, and brain rise in blood sugar increased metabolic rate bronchi dilate pupils dilate hair stands on end ("gooseflesh" in humans) clotting time of the blood is reduced increased ACTH secretion from the anterior lobe of the pituitary. All of these effects prepare the body to take immediate and vigorous action. source: http://www.mmra.org/~jkimball/BiologyPages/A/Adrenals.html#adrenaline ARTICLE 2------------------------------------------------------------------ Cornell University 18-Apr-98 Molecular Memory Tunes Adrenalin to Stress Library: MED Keywords: ADRENALINE EPINEPHRINE ADRENAL GLAND STRESS MEMORY MOLECULAR CORNELL Description: Cornell University neurobiologists, studying the adrenal glands of rats, have discovered how chronic stress cranks up the intensity of thes adrenaline response. The key to this so-called molecular memory resides in a donut-shaped protein on the surface of cells that secrete adrenaline, the hormone also known as epinephrine. FOR RELEASE: April 17, 1998 Contact: Roger Segelken Office: (607) 255-9736 Internet: hrs2@cornell.edu Compuserve: Bill Steele, 72650,565 http://www.news.cornell.edu ITHACA, N.Y. -- In the rat race of life, a sudden demand from the boss can trigger an adrenaline surge that quickens your pulse, raises blood pressure, kick-starts anxiety and prepares you for "fight or flight." Now Cornell University neurobiologists, studying the adrenal glands of rats, have discovered how chronic stress cranks up the intensity of this adrenaline response. The key to this so-called molecular memory resides in a donut-shaped protein on the surface of cells that secrete adrenaline, the hormone also known as epinephrine. "The hormonal response to stress is different for every individual, and seems to be controlled by some combination of inheritance and lifestyle," explains David P. McCobb, co-author along with Jiuyong Xie of a report in the April 17 issue of the journal Science. "Our study points to the effect of lifestyle. Stressful experience is remembered, and biases us toward responding forcefully to subsequent threats," McCobb says. Improved understanding of chemical signaling cascades in the endocrine system could lead to better medical therapies -- perhaps even gene therapy -- for conditions such as hypertension and heart attack, predict McCobb, an assistant professor of neurobiology and behavior, and Xie, a postdoctoral researcher in the McCobb's department. "Whether our stress responses are controlled by genes or lifestyle, we'd like to have more control," McCobb says. "We don't want to secrete more adrenaline than necessary. There's a definite adaptive advantage to being able to back off." The Cornell researchers report that adrenal cells dump adrenaline into the blood at a rate that is determined not only by the necessary incoming neural signals from the brain, but also by the intrinsic electrical excitability of the adrenal cells themselves. That excitability is determined by the structural detail of the donut-shaped channel proteins that allow potassium electrical signals to cross the cell membrane. And the structural detail is controlled at the gene level by steroids, according to the researchers. Forceful heart, lung, metabolic and behavioral reactions help cope with acute threats, McCobb says, "but those reactions are not healthful in the long run. We found that steroid stress hormones dictate whether the potassium channels controlling adrenaline release are constructed with or without an optional piece called STREX, for stress exon. This STREX exon causes the channel to open more easily, which favors rapid, excitable responses and fast secretion of adrenaline." To test the theory, the Cornell researchers surgically removed several rats' pituitary glands, the source of ACTH (adrenocorticotropic hormone), a key link in the stress hormone cascade. Without pituitary glands, the percentage of STREX-type channels dropped sharply. This was prevented by injecting ACTH artificially. Source: http://www.newswise.com/articles/1998/4/ADRENAL.CNS.html --------------------------------------------------------------------------- Links: http://www.stmarys.medford.or.us/curriculum/bio/hbsm/glands/adrenal.htm http://www.ncbi.nlm.nih.gov/PubMed/ If you type "adrenaline", you get close to 90,000 hits! --------------------------------------------------------------------------- I hope this helps. If you are looking for something more specific, then send your question and I will be glad to respond. Arash E. Genetics UBC
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