Pegasys Enzyme Link Explanation
Pegasus,
I have seen that link before (possibally by you) and i would just like to thank you for putting it up there. Anyways I know this has not much to do with lorazepam, but let me throw something in for people that don't know. Lorazepam does not have an active metabolite. So be careful in building your body chalk full of inactive metabolites. Also Im pretty sure pegasus must have posted this somewhere else instead. Actually now that I look down I see the quote kind of mentions that. So for all you people who wish to potentiate your drugs with liver metabolism I urge you to read the .pdf link at the bottom of the paper. A few things you should know.
Substrate- This is the main drug that can either be induced by the certain enzyme (being cyp3a4) in this example or induced by the liver enzyme meaning that the 3a4 enzme is halted from production therefore letting the drug either last longer (the substrate) or get you higher, all depening on eith half life, active, inactive metabolite etc.
Inhibitor As I stated this before it stops the specific liver enzyme for being produced for a certain amount of time.
Inducers These medicines will cause the substrate to be destroyed faster as the enzyme that is being induced breaks down the parent compound very fast.
Now let me put this all down in lamens form via example: The substrate would be alprazolam. Now this system uses the p450 3a4 enzymes. So you use say cimetidine (a potent cyp3a4 inhibitor), You will have a longer blood half life and it will keep the ACTIVE enzyme of alprazolam from being destroyed much too rapidly. Now say you take concurrently an inducer with alprazolam i.e. prednisone, it will cause the partent drug along with the active metabolite to be destroyed at a much faster rate.
One more note: The inhibitors in in the 3a4 system are most of the time stronger than the ones in plain font. The same with inducers (meaning they are stonger than their counter points. A substrate in paranthesis I belive either is affected harder by the inhibitors or inducers or I can be wrong, it might mean that they have active metabolites (Im not sure I didnt write the chart. One warning, try not to be eating bowls of tagamet for breakfast as you will damage your body, and I cant imagine that all of this liver magic could possibally be good for you. I usually use the p4503a4 system to make my opiods an certains benzos stronger (This is especially good with alprazolam because first off it has a short half life as it is, second if you smoke the alprazolam already is being cut down from the nicoteine.) Just remember guys taking a whole bunch of grapefruit juice, cimetidine, alprazolam, fentanyl , and alfentanyl is a suicide just waiting to take place . Any questions please email me at
[email protected] ALso here is the original chart, not sure if it originated from pegasus or whomever before him, but I am not taking credit. Just trying to help people who might not understand this kind of thing.
Also, does anyone
HAVE ANY INFO AT ALL on the enzyme systems of phenazepam?? Im having a hard time finding it but im kinda multasking.. If you can find the russian pharmacoepia you might find it there. Thank you for your time and dont forget your body is sacred, dont destroy your live so you can get an extra 15 minutes off your suboxone.
MAILTO QUESTIONS AND ANSWERD FROM sp0r:
[email protected]
[email protected] cricket.com <-- You can send a multi media message to my phone via this address if the txt will be 100 characters or more.
Send to this address if you have a showt question or answer ~ 60-80 character. I Ill reply as soon as I can. I love to help people out.
aim: dag109
GFJ/ cimetidine would not potentiate lorazepam, as CH said...
ps- Pegasys thanks for posting that chart it has helped ALOTl%)