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Antipyretic-Analgesic and Antiinflammatory Drugs. A. General Pharmacological properties. 1. Inhibition of prostaglandin synthesis inhibiting cyclooxygenase (COX ,环氧酶 ), decreasing the synthesis of PGs and TXA 2 , resulting antipyretic, analgesic, and anti-inflammatory effects
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A. General Pharmacological properties • 1. Inhibition of prostaglandin synthesis • inhibitingcyclooxygenase (COX,环氧酶), • decreasing the synthesis of PGs and TXA2, • resulting antipyretic, analgesic, and anti-inflammatory effects • non-steroidal anti-inflammatory drugs (NSAIDs, 非甾体抗炎药)。
A. General Pharmacological properties • 2. Antipyretic effects • Inhibition of PGE2 production in the hypothalamus induced by endogenous pyregens after pathological stimuli temperature • notes:symptomatic control only, not be indicated in all patients with fever. • The effect on body temperature is different from that of chlorpromazine.
A. General Pharmacological properties • 3. Analgesic effects • Analgesic effect is resulted from inhibition of PGE2 production. • Effective on the pain of low to moderate intensity related to inflammatory responses. • PGE2: a pain stimulant and hyperalgesic agent • The analgesic effect is different from opioid analgesics.
A. General Pharmacological properties • 4. Anti-inflammatory effects • PGs induce inflammatory responses. • Inhibition of PG production can relieve inflammatory responses, such as congestion, exudation, pain. • The effect is different from that of glucocorticosteroids.
A. General Pharmacological properties • 5. COX-1 / COX-2 and selectivity of the drugs • COX-1:constructive;involved in physiologic regulatory functions in GI tract, kidney, etc.; • inhibition of COX-1 is related to the adverse effects. • COX-2:inducible; involved in pathological responses such as inflammation, and pregnancy; • inhibition of COX-2 is related to the therapeutic effects.
(-) (+) (+) (-)
B. Salicylates Aspirin 阿司匹林 Acetylsalicylic acid 乙酰水杨酸 Salicylic acid 水杨酸 Salicylic sodium 水杨酸钠 Aspirin 阿司匹林
B. Salicylates • Aspirin 阿司匹林 • 1. ADME • transformed to salicylic acid form in the body • hepatic metabolism is primarily conjugation. • excretion from urine, the excretion of unchanged forms of aspirin is increased in the alkalinized urine. • larger doses ( > 1g/d):non-linear elimination, zero order kinetic process, easier to accumulation and intoxication.
B. Salicylates • 2. Pharmacological effects and clinical uses • (1) Antipyretic, analgesic and anti-inflammatory effects • moderate doses (0.3~0.6 g): antipyretic and analgesic effects • larger doses (3~5 g/d): anti-inflammatory and anti-rheumatic effects; only relieves symptoms. • to treat acute rheumatic fever(急性风湿热), • to abate pain and symptoms of rheumatic & rheumatoid arthritis (风湿性和类风湿性关节炎).
B. Salicylates • (2) Inhibition of platelet aggregation • small doses (30~100 mg/d): inhibiting TXA2 synthesis, preventing thrombosis. • used to treat ischemic heart disease, reduce the mortality of myocardiac infarction, and prevent cerebral thrombosis. • larger doses: inhibiting PGI2 synthesis, promoting thrombosis. • PGI2: vasodilation and platelet depolymerization (血小板解聚).
The mechanism of aspirin: Target enzymes acetylated
B. Salicylates • 3. Adverse effects • (1) GI reactions • stimulating gastric mucosa and CTZ (larger doses); • inhibiting PG synthesis in GI tract • irritant symptoms; gastric bleeding; ulcerous disorders Contraindications: ulcerous disorders
B. Salicylates • (2) Prolongation of bleeding time • small doses: inhibiting platelet aggregation • larger doses: inhibiting synthesis of thrombogen Contraindications: one week prior to surgery; severe hepatic damage; vitamin K deficiency,; prothrombinopenia (凝血酶原减少症).
B. Salicylates • (3) Allergic reactions • urticaria(荨麻疹), • angioneurotic edema, • aspirin-induced asthma, • occasionally anaphylactic shock. • Contraindications:bronchial asthma
Aspirin-induced asthma: Phospholipids of cell menbrane AspirinPhospholipase A2 (PLA2) (-) Arachidonic acid Cyclooxygenase Lipoxygenenase (环氧酶) PGH2 5-HPETE (脂氧酶) ↓Prostaglandins (PGs)↑Leukotrienes (LTs) (前列腺素)(白三烯)
B. Salicylates • (4) Salicylism dose > 5g/d: CNS symptoms, including mental confusion; hyperventilation. i.v. NaHCO3 can promote the excretion of aspirin. • (5) Hepatic damage • Overdose: hepatic damage Reye’s syndrome(瑞夷综合征): in children, severe hepatic damage (严重的肝损害) and encephalopathy (脑病)
Dose-response relationship of aspirin: therapeutic effects; adverse effects
B. Salicylates 4. Drug interactions
C. Para-aminophenol derivatives Acetaminophen 对乙酰氨基酚 Paracetamol扑热息痛
C. Para-aminophenol derivatives • Acetaminophen (对乙酰氨基酚): • antipyretic and analgesic effects are mild and lasting, but almost no anti-inflammatory effects, - not aNSAID • higher selectivity to COX in CNS. mainly used in cold, fever, and headache, etc. overdose can damage liver and kidney.
D. Other anti-inflammatory drugs Salicylates: aspirin Para-aminophenol derivatives: acetaminophen Indole and indene acetic acid derivatives: indomethacin, sulindac Propionic acid derivatives: ibuprofen, naproxen, fenopofen, ketoprofen COX-2 selective inhibitors: meloxicam, celecoxide, rofenxid Others: phenylbutazone, diclofenac
indomethacin 吲哚美辛 ibuprofen 布 洛 芬 piloxicam 吡罗昔康
D. Other anti-inflammatory drugs • indomethacin 吲哚美辛:stronger efficacy, controlling special types of fever; severe adverse effects • ibuprofen 布洛芬(芬必得):stronger antipyretic, analgesic and anti-inflammatoryeffects; weaker GI reactions; vision damage • piloxicam 吡罗昔康:long-acting anti-inflammatory and analgesic agent; long-term use induces hemorrhage and ulcers in GI tract
COX-2 selective anti-inflammatory drugs Meloxicam 美洛昔康 stronger effect on COX-2 than COX-1 long-acting (t1/2 20 h) weaker GI reactions