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  1. BlueMystic
    Know Thy Poison
    Author: Robert S. Gable
    American Scientist
    Published: Tuesday, May 30, 2006

    The Shuar tribes in Ecuador have for centuries used native plants to induce religious intoxication and to discipline recalcitrant children. By comparison, most North Americans know little about the mood-altering potential of the wild vegetation around them. And those who think they know something are often dangerously ignorant. Over a three-week period in 1983, for example, 22 Marines wanting to get high were hospitalized because they ate too many seeds of the jimsonweed plant (Datura stramonium), which they found growing wild near their base, Camp Pendleton in southern California.

    A dozen seeds of jimsonweed contain about one gram of atropine, 10 grams of which can cause nausea, severe agitation, dilation of pupils, hallucinations, headache and delirium. Tribal groups in South America refer to datura plants as the "evil eagles." Of approximately 150 hallucinogenic plants that are routinely consumed around the world, those with atropine have the worst reputation.

    An easier way to learn about the risk posed by a substance is through careful laboratory study. The first example of such an exercise, in 1927, used rodents. Research toxicologist John Trevan published an influential paper that reported the use of more than 900 mice to assess the lethality of, among other things, cocaine. As he and others have since found, a substance that is tolerated or even beneficial in small quantities often has harmful effects at higher levels.

    The amount of a substance that produces a beneficial effect in 50% of a group of animals is called the median effective dose. The quantity that produces mortality in 50% of a group of animals is termed the median lethal dose.

    Laboratory tests with animals can give a general picture of the potency of a substance, but generalizing experimental results from, say, mice to humans is always suspect. Thus toxicologists also use two other sources of information. The first is survey data collected from poison-control centres, hospital emergency departments and coroners' offices. Another consists of published clinical and forensic reports of fatalities or near-fatalities.

    But these sources, like animal studies, have their limitations. Simply tallying the number of people who die or who show up at emergency rooms is, by itself, meaningless because the number of such incidents will be influenced by the total number of people using a particular substance, something that is impossible to know. For example, atropine is more toxic than alcohol, but more deaths will be reported for alcohol than for atropine because so many more people get drunk than ingest jimsonweed. Furthermore, most overdose fatalities involve the use of two or more substances (usually including alcohol), situations for which the overall toxicity is largely unknown.

    How then does one gauge the relative risks of different recreational drugs? One way is to consider the ratio of effective dose to lethal dose. For example, a normally healthy 70-kilogram adult can achieve a relaxed affability from approximately 33 grams of ethyl alcohol, the amount contained in two 1.5-ounce shots of 80-proof vodka. The median lethal dose for such an adult is approximately 330 grams, the quantity contained in about 20 shots of vodka. A person who consumes that much (10 times the median effective dose), taken within a few minutes on an empty stomach, risks a lethal reaction. And plenty of people have died this way.

    In analyzing the lethality of a given psychoactive substance, the method of absorption is a critical factor. The common routes of consumption, from the least toxic to the most toxic (in general), are: eating or drinking a substance, depositing it inside the nostril, breathing or smoking it, and injecting it into a vein with a hypodermic syringe. So, for example, smoking methamphetamine (as is done with the popular illicit drug "crystal meth") is more dangerous than ingesting it.

    The most toxic recreational drugs, such as GHB (gamma-hydroxybutyrate) and heroin, have a lethal dose less than 10 times their typical effective dose. The largest cluster of substances has a lethal dose that is 10 to 20 times the effective dose: These include cocaine, MDMA (methylenedioxymethamphetamine, often called "ecstasy") and alcohol.

    A less toxic group of substances, requiring 20 to 80 times the effective dose to cause death, include Rohypnol (flunitrazepam or "roofies") and mescaline (peyote cactus).

    The least physiologically toxic substances, those requiring 100 to 1,000 times the effective dose to cause death, include psilocybin mushrooms and marijuana, when ingested. (I've found no published cases in the English language that document deaths from smoked marijuana, so the actual lethal dose is a mystery.)

    Alcohol thus ranks at the dangerous end of the toxicity spectrum. So despite the fact that about 75% of North American adults enjoy an occasional drink, it must be remembered that alcohol is quite toxic. Indeed, if alcohol were a newly formulated beverage, its high toxicity and addiction potential would surely prevent it from being marketed as a food or drug.

    Most of us have not had a life-threatening experience with alcohol. Yet statistics show that every year about 300 people die in the United States from an alcohol overdose -- and for at least twice that number of overdose deaths, alcohol is considered a contributing cause.

    One reason people feel comfortable with alcohol is that individuals have reasonably good control of the quantity they consume. Certainly, control of one's dose of alcohol is easier than with many natural or illicit substances for which the active ingredients are not commercially standardized.

    Furthermore, alcohol is almost always consumed in a highly diluted form. The stomach capacity of an average adult is about one litre; therefore, a person is unlikely to overdose after drinking beer containing 5% alcohol.

    A simpleminded look at the ratio of effective to lethal doses ignores some complications, however. Take, for example, the fact that danger generally increases with repetitive consumption. High blood levels of a drug, without rest periods between use, tend to heighten risk, because the affected organs do not have sufficient time to recover.

    Studies of MDMA use, for example, show that relatively small repeated doses result in disproportionately large increases of MDMA in blood plasma. Cocaine is the substance that induces the highest rate of repetitive consumption as a result of mood change. Heroin and alcohol come in second and third.

    Also, the tendency of a user to take a "booster" dose prematurely is greater with substances that require an hour or more to provide the full psychological effect -- during the interim the user often assumes that the original dose was not sufficiently potent. This phenomenon routinely occurs with dextromethorphan (found in cough medicines), GHB and MDMA.

    Overdose quantities that are based on acute toxicity also do not take into account the probability that an individual will become addicted. This probability can be cast as a drug's capture ratio: Of the people who sample a particular substance, what portion will become physiologically or psychologically dependent on the drug for some period of time? Heroin and methamphetamine are the most addictive by this measure. Cocaine, pentobarbital (a fast-acting sedative), nicotine and alcohol are next, followed by marijuana and possibly caffeine. Some hallucinogens -- notably LSD, mescaline and psilocybin -- have little or no potential for creating dependence.

    Finally, a comparison of overdose fatalities does not take into account cognitive impairments and risky or aggressive behaviours that sometimes follow drug use. And as most people are well aware, a substantial proportion of violent confrontations, rapes, suicides, automobile accidents and AIDS-related illnesses are linked to alcohol intoxication.

    Despite the health risks and social costs, consciousness-altering chemicals have been used for centuries in almost all cultures. So it would be unrealistic to expect that all types of recreational drug use will suddenly cease. Self-management of these substances is extremely difficult, yet modern Western societies have not, in general, developed effective methods for regulating their use.

    The science of toxicology may provide one step in that direction -- by helping to teach members of our society what a lot of tribal people already know.

Comments

  1. Nagognog2
    "A dozen seeds of jimsonweed contain about one gram of atropine, 10 grams of which can cause nausea, severe agitation, dilation of pupils, hallucinations, headache and delirium."

    This is not true at all. The amounts are WAY off as 12 seeds don't even approach weighing a gram total. More like 10 MILLIGRAMS of atropine will cause poisoning. And the fatal dose of MDMA is way off as well.

    Interesting article, but the writer does not know weights and measures.
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