Just as we all don’t wear the same sized sweater, so too are medication dosages not meant to be one-size-fits-all proposition. Physiologically, a 100-pound woman and a 200-pound man process the same dosage differently, so it’s important to follow medication directions, for both over-the-counter and prescription drugs.
The liver takes in raw materials and produces all sorts of products we need to live. It is also a purification plant that takes in toxic waste for elimination while cleaning some substances and sending them out for further use. This article is about the medications we take and the toxic components built into them by science, knowing that a particular enzyme system in the liver, cytochrome P450 (CYP450), will clear them in the liver.
Pharmacology is the study of the actions of drugs on biological systems. These drugs either activate (agonists) or inhibit (antagonists) normal physiological processes. For example, selective serotonin reuptake inhibitors (SSRI’s), one kind of anti-depressant drugs, are designed to affect biological activity through inhibition.
When developing a drug, scientists ascertain its therapeutic use measuring pharmacokinetics-dosage and the absorption, distribution, metabolism, and excretion in and through the body, and pharmacodynamics- how the drug acts on the body.
By the time a drug makes it to the market, it has been well-tested to make it safe for public consumption. Very basically, the measure known as the Area Under the Curve (AUC), measures the movement of a substance into and through the body, depicting the time of its greatest concentration.
This copious testing takes into account how long it takes for the body to eliminate one-half life of the drug from the body and then how much is left in the body after five half-lives. For example, if 100 mg has a half-life of 50 mg, then its subsequent half-lives will be 25 mg, 12.5 mg, 6.25 mg, and 3.125 mg, respectively. This is why some drugs you may take require several weeks of regular dosage before achieving correct concentration in the blood, body fluids, or tissue for a therapeutic effect, and others go directly to the targeted area and have an immediate effect.
Cytochrome P450 is the generic name for a group of enzymes clustered in the liver and small intestines that breaks down anything the body doesn’t want hanging around in active form, including things eaten such as food and herbs. Two major points to remember regarding the CYP450 enzyme system are:
1) More is NOT better- CYP450 can process only so much at a time, and
2) Herbs and prescription drug should be taken two hours apart to minimize interaction
Here’s why:
As mentioned above, certain drugs are designed to increase the activity of CYP450 and others inhibit it so that the drug can stay in the body longer.
1) Some chemical reactions in the body are additive: for example, substance A combines with substance B, or 2 + 2 = 4.
2) Some chemical reactions in the body are synergistic: for example, substance A combines with substance B to produce a stronger effect by staying in the body longer, so that 2 + 2 = 10.
3) And, some chemical reactions in the body inhibit each other or cancel each other out: for example, substance A combines with substance B, or 2 + 2 = .05 or 2 + 2 =. These include certain foods and herbs, which can interact with certain drugs and get in the way of CYP450 either additively, synergistically, or by inhibiting ts functions.
Therefore, it is important to take follow dosage recommendations, and to not overtax the liver by asking it to process too many medically-intended substances at once: think twice next time you reach for something, asking yourself if you really need it. If you say “yes,” remember what else you ate or in the past hour, and maybe wait a bit, or take a lesser dosage and see how that works.
http://mountaintopacupuncture.com/cytochrome-p450-one-tablet-or-two
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