IHateFin
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Here is a VERY good paper demonstrating what naltrexone actually does. I uploaded the OP with the link as well. REBOUND = SNAP BACK
Below includes a short excerpt of the paper. I will also include the link for the full paper here.
The mechanism of action of naltrexone, in autoimmune diseases and cancer, is still being researched, but there are theories as to the mechanism of action that both explain why LDN works on both autoimmune diseases and cancers, as well as inflammatory disease. According to Mark J. Donahue’s paper on LDN that uses interviews from Dr. David, Gluck, Dr. Jacquelyn McCandless, Dr. Jarred Younger, and Dr. Ian Zagon: “LDN is an opioid antagonist that not only blocks the reception of opiates, but also the body’s own endogenous opioids – endorphins. However, because LDN is administered in such a 'low dose' it is believed that LDN only briefly (for 3-4 hours) obstructs the effects of endorphins. Sensing an endorphin deficit, the hypothalamus signals for increased production of endorphins in what is called 'the rebound effect.'
The rebound effect results in three things happening:
- Opioid receptor production increases in order to try and capture more endorphins.
- Opioid receptor sensitivity increases, also in order to try and capture more endorphins.
- Production of endorphins is increased in order to compensate for the perceived shortage.
Once LDN is metabolized by the liver and eliminated from the body (after 3-4 hours), the elevated levels of endorphins produced, as a result of the rebound effect, can now interact and bind with the more sensitive and more plentiful opioid receptors. These opioid receptors, are found throughout the body, including virtually every cell of the body’s immune system. The elevated levels of endorphins will usually last around 18-20 hours. During this time the elevated endorphins act by up-regulating vital elements of the body’s immune cells. By doing so clinical trials has been shown that elevated levels of
- Down regulating inflammatory cytokines
- Reducing inflammation and oxidative stress
- Facilitating tissue repair and wound healing
- Restoring T-helper/CD4 levels
- Restoring the balance between Th1 & Th2 lymphocytes
- Increasing cytotoxic T cells and natural killer (NK) cells
- Regulating cell growth & inhibiting tumor growth
- Reducing excitotoxicity and microglial activation
- Reducing apoptosis of the myelin-producing oligodendrocytes
- Stimulating mucosal healing (lining of bowel)” 7
I'm excited!!