How do different analgesics prevent pain?. What is pain? pain |pān|noun physical suffering or discomfort caused by illness or injury : she's in great.

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Presentation transcript:

How do different analgesics prevent pain?

What is pain? pain |pān|noun physical suffering or discomfort caused by illness or injury : she's in great pain | those who suffer from back pain. a feeling of marked discomfort in a particular part of the body : he had severe pains in his stomach | chest pains. mental suffering or distress : the pain of loss.

How do we feel pain? Pain receptors in our bodies are nerves that transmit pain. These are free nerve endings located in various body tissues that respond to thermal, mechanical and chemical stimuli. When stimulated, these pain receptors generate an impulse. The pain results of various impulses arriving at the spinal cord and the brain. When tissues become injured, they release chemicals called prostaglandins and leukotrienes that make the pain receptors more sensitive and thus causing pain.

Painkillers already in your body They are produced naturally in the body. Endorphins and enkephalins are the natural opiates found in the part of the brain and the spinal cord that transmit pain impulses. They are able to bind to neuro-receptors in the brain and produce relief from pain. The temporary loss of pain immediately after an injury is associated with the production of these chemicals.

Analgesics Drugs that relieve pain Mild analgesics: used for relief of mild pain. (aspirin, acetaminophen) Strong analgesics: used for relief of vary severe pain.(morphine, heroin, codeine) Local anesthetics: used as pain killers in localized areas.(lidocaine, procaine) General anesthetics

Mild analgesics Used to treat mild pain Mild analgesics function by intercepting the pain stimulus at the source, often by interfering with the production of substances (for example, prostaglandins). Constricts blood vessels near the pain source reducing inflammation. Prevent an increase in body temperature that causes fever.

Aspirin (salicylic acid) Aspirin also has anti blood clotting properties and so is used in the treatment of heart heart or stoke. Acetaminophen and ibuprofen do not do this.

Disadvantages of aspirin Aspirin can cause stomach upset and internal bleeding due to its acidic nature. There is a risk of developing severe gastrointestinal bleeding following use of alcohol. 0,5% are allergic to aspirin leading to skin rashes, respiratory difficulty and even shock Aspirin is one of the most frequent causes of accidental poisoning in infants. The taking of aspirin by children under twelve has been linked to Reye’s disease (a fatal liver and brain disorder with the symptoms of vomiting, lethargy, irritability and confusion.)

Acetaminophen and Ibuprofen Acetaminophen is not an effective anti inflammatory drug. It is a safe drug when it is used in the correct dose BUT can rarely cause side effect such as blood disorders and kidney damage. In great dose (>20 tablets) can cause serious liver damage, brain damage, coma and even death. Ibuprofen has many of the same effects as aspirin but seems to cause fewer stomach problems. It is an anti-inflammatory drug. It is effective in low doses and has a wide margin of safety. In great dose has similar side effects as aceteaminophen.

Strong analgesics Temporarily bind to the opiate receptor sites in the brain preventing the transition of pain impulses between brain cells Mimic the body's own natural painkillers (endorphins and enkephalins) producing analgesia (a sense of well being).

Terms Opiate: a natural or synthetic drug that exerts actions on the body similar to those induced by morphine. Narcotic: a term generally used for drugs that have both a narcotic and analgesic action.

Opiates

Morphine, Heroin, Codeine

ACETYL, BETA-ENDORPHIN (1-26), HUMAN

Morphine is the principal alkaloid and makes up about 10% by mass of raw opium. Codeine makes up about 0.5% by mass of raw opium. Heroin is usually synthesized from morphine and thus is a semi-synthetic drug and it is obtained by relatively simple structural modification of morphine or codeine.

Pharmacological effects Opiates exert major effects on: The central nervous system. The eye The gastrointestinal tract (the digestive system) The prime medical uses of opiates are: As strong analgesic in the relief of severe pain caused by injury and chronic disease. In the treatment of diarrhea by producing a constipating effect. To relieve coughing by suppressing the “cough center” situated in the brain system.

Physiological effects Opiates produce: Analgesia Drowsiness Mood changes Medical clouding Some individuals experience: Anxiety Fear Lethargy Sedation Lack of concern Inability to concentrate

Tolerance Tolerance appears due to the induction of drug metabolizing enzymes in the liver and also to the adaptation of neurons in the brain to the presence of the drug. The users that became tolerant to one opiate will also exhibit a tolerance to all other opiates.

Dependence and adiction Physical dependence is the state in which people do not function properly without a drug. Depends on: The dose Frequency of drug administration The duration of the drug dependence The opiate used

Withdrawal symptoms Symptoms: Restlessness Sweating Fever Chills Vomiting Increase rate of respiration Cramping Diarrhea Unbearable aches Do the benefits outweigh the risks?