Opiates/opioids effects

Administration of naloxone prevents or reverses the effects of the opiates. The exact mechanism of action is not fully understood, but it is believed that naloxone reverses opioid effects by competing for opiate receptor sites (see Chap. 19). If the individual has taken or received an opiate, the effects of the opiate are reversed. 

Semisynthetic and synthetic narcotics are also produced that have opiate-like effects these narcotics are collectively known as opioids. They include methadone and the designer drug fentanyl, and a number of commonly prescribed medicines such as Darvon, Demerol, Dilaudid, Orlaam, OxyContin, Percodan, Talwin, and Vicodin. 

A study involving 16 opioid-dependent subjects found that amprenavir 1.2 g twice daily for 10 days decreased the AUCs for both f -methadone (active enantiomer) and 5-methadone (inactive enantiomer) by 13% and 40%, respectively. No clinically significant changes were noted in opioid effects and there was no evidence of opioid withdrawal. However, in another study methadone levels were reduced by 35% (range 28% to 87%) in 5 patients within 17 days of starting to take amprenavir 1.2 g twice daily and abacavir 600 mg twice daily. Two patients reported nausea before their daily methadone dose, which can be a sign of opiate withdrawal. Note that abacavir , (p.l75), may modestly reduce methadone levels, and could therefore have contributed to this effect. 

Enkephalins and Endorphins. Morphine (142), an alkaloid found in opium, was first isolated in the early nineteenth century and widely used in patent medicines of that eta. It is pharmacologically potent and includes analgesic and mood altering effects. Endogenous opiates, the enkephalins, endorphins, and dynotphins were identified in the mid-1970s (3,51) (see Opioids, endogenous). Enkephalins and endorphins ate Hsted in Table 9. 

Opiate overdose is a medical emergency that can result in respiratory and CNS depression. The opioid receptor antagonist naloxone immediately reverses cardiorespiratory depression. However, repeated naloxone administration is required, since the effects of naloxone last for 30 min, while opioid agonists can remain at potentially lethal blood levels for several hours. 

The pharmacological and/or adverse effects of a drug can be reversed by co-administration of drugs which compete for the same receptor. For example, an opioid receptor antagonist naloxone is used to reverse the effects of opiates. Drugs acting at the same site with opposite effects also can affect each other, e.g. the reduction in the anticoagulant effect of warfarin by vitamin K. 

In the strict sense, opiates are drugs which are derived from opium and include the natural products morphine, codeine, thebaine and many semi-synthetic congeners derived from them. In the wider sense, opiates are morphine-like drugs with non-peptidic structures. The old term opiates is now more and more replaced by the term opioids which applies to any substance, whether endogenous or synthetic, pqrtidic or non-peptidic, that produces morphine-like effects through an action on opioid receptors. 

Two opioids are used in the treatment and management of opiate dependence levomethadyl and methadone. Levomethadyl is given in an opiate dependency clinic to maintain control over the delivery of the drug. Because of its potential for serious and life-threatening proarrhythmic effects, levomethadyl is reserved for use in the treatment of addicted patients who have no response to other treatments. Levomethadyl is not taken daily the drug is administered three times a week (Monday/Wednesday/Thursday or Tuesday/Thursday/ Saturday). Daily use of the usual dose will cause serious overdose. 

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