guards said:
Darksun, you obviously have no idea what you are talking about. Pain killers affect the hypothalmus which is your pleasure center and the center that releases dopamine and serotonin..........the naturlaly occuring drugs that regulate pain relief and circadian rhythms. AS has nothing to do with the hypothalamus, AS affects the pituatary gland the cerebral cortex with the added release of testosterone or estrogen in various forms. The TOLERAANCE to AS is because your body is fooled into thinking that it has enough test in it, therefor stopping production. So that when you start a new cycle, you have to replace the amount that your body stopped producing and add the amount desired for the effect.
Damn I'm good....................psych degree really IS good for something.
My 2 cents
I just stumbled on this thread so I'm going to take it from the top. Pain killers don't work by regulating serotonin and dopime. They have nothing to with that.
Neurons are fed information by dendrites. Once there is enough information to merit a particular response (response threshold) the axon bulb releases a brief spurt of K+ which causes the doors/chambers of the axon to fire open. Each time a chamber opens, through a chain reaction, it causes the next door to open. When these doors open, K+ and Cl- rush out and Na+ rushes in. The nerve is then in cabable of firing again until the K+ and Cl- can seep back into the axon chambers and the Na+ is pumped out by the sodium/potassium pump. The sodium/potassium pump is powered by ATP.
What a pain killer does is occupy the sodium/potassium pump and prevents the active transport of Na+ from within the axon chambers after the neuron has fired. This slows the influx of K+ and Cl- wich leaves the neuron unable to fire for longer periods of time. If the neuron can't fire, it can't send a message of pain. If it can't send the messsage, the brain doesn't know that there is injury or trama. The stronger the pain killer, the more it prevents the actions of the sodium/potassium pump and the more it prevents the pain sensations.
These medications are metabolised by the liver. The more the liver comes into contact with this pain killer substance, the more enzymes that it makes that are capable of breakikng it down. The purpose behind this is the body doesn't want to be hindered. It wants to reach a homemostasis and do what it was meant to do. Our bodies adapt. So one would have to use more and more pain killer to get the same effects because more is becoming "destroyed" by the liver.
The same holds true for any recreational drug that is metabolised by the liver i.e. alchohol, cocaine, etc. The same is also true for caffeine and most any drug or medication availible. The higher quantity that you take, the quicker you will develop a tolerance (efficency of the liver to metabolise) to normal amounts.
The same is true for anabolic steroids. The further the levels get from your normal baseline, the harder you liver works to metabolise them. Whenever the levels are remaining high for a long time, eventually the liver becomes so efficient that it is destroying/breakign down the AS before the androgen even has a chance to bind to its appropriate receptors and elicit its anabolic response. It does this in an effort to get levels to return to baseline. Thus, higher and higher dossages must be used in order to have the same response that one once had for low dosses.
Receptors do not down regulate. They upregulate in response to high levels of hormone. Receptors are like the epithelial cells in that they are constantly changing (dying and growing back). Gear looses its effectiveness through the ability of the body to break it down in an effort to return hormone levels to baseline.
-Stew