1 welcome to pharmacology. 2 chapter 21 analgesics
TRANSCRIPT
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Welcome to Pharmacology
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Chapter 21 Analgesics
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Overview
Section 1
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two components
somatic sensation
affective (emotion)
1. Concept
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52. Pain transmission pathway
Noxious stimuli
PGs
K+ 、 H+
BK
5-HT
Primary afferent fibres (C/Aδ)
nociceptor
Spinal cord
Limbic system
Somato-sensory cortex
mood effect, the affective aspect of pain
the sensory aspect of pain
Medulla
Midbrain
Dorsal horn
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Descending pain inhibitorypathways
Local inhibitory interneuron in spinal cord
Pain
Ascending pain transmission pathways
Endogenous opioid peptides
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Medulla
Midbrain
Cortex
Spinal cord
Dorsal horn
Ventral caudal thalamus
PGs
K+ 、 H+
BK
5-HT
NSAIDs
Local anesthetics
Opioid analgesics , Antidepressants and General
anaesthetics
Sites of action of different drugs
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Pain
a. Acute pain (sharp pain), superficial pai
n, quick response of sudden onset, con
ducted by A nerve fibers
b. Chronic pain (dull pain), more lingerin
g and aching, conducted
by C nerve fibers
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severe, sharp painopioid analgesics
(eg. Morphine)
inflammation, elevated temperature, chronic- dull pain
NSAIDs
(eg. Aspirin)
smooth muscle colic
(eg. biliary or renal colic)
angina pectoris induced by coronary artery spasm
trigeminal pain
3. Durg treatment of pain
cholinoceptor-blocking drugs (eg. Atropine)
vasodilator drugs (eg. Nitroglycerin)
Carbamazepine
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Analgesics
Drugs which act on CNS , could rel
ieve or alleviate severe pain and un
happy mood without affecting othe
r sense perception, and consciousn
ess
1. Concept
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Full agonist of opioid receptors
Partial agonist of opioid receptors
Other analgesics
2. Classification
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Section 2Section 2
Full agonist of opioid receptors
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Opium Alkaloids
• Phenanthrenes
morphine, codeine
• Benzylisoquimolines
papaverine
--has no analgesic effect
--dilates the vessel
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14 The flower of papaver somniferum
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15Opium
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Morphine
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1803 Serturner isolated a pure active alkaline substance from opium .
He proposed the name“morphine”for it after Morpheus.
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structure-activity relationshipstructure-activity relationship
海洛因
吗啡
纳洛酮
OH
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Pharmacokineticsabsorption excretion distribution
free drug
oral First pass elimination
sc. im.
blood
liver
placental fetuslittle cross
the BBB, but enough for its function
metabolism
morphine-6-glucuronide
kidney, breast
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Pharmacological actions
1. CNS
2. Smooth muscles
3. Cardiovascular system
4. Others
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Pharmacological actions
1.CNS effects :principal effects
analgesia
euphoria
sedation
respiratory depression
tolerance
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(1) Analgesia powerful pain-relieving effect
all types of pains:
* constant, dull ﹥intermittent, sharp
poor efficiency on neuropathic pain
without affecting consciousness and
other sense perception
duration : 4-6h
1. CNS
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(2) Sedation and euphoria
tolerance of pain
drowsiness and clouding of mentation
sleep induced and aroused easily
*Euphoria
a sense of contentment and well-being
relieve anxiety and distress
Sedation
the main reason for drug abuse
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Activate the opioid receptor at limbic sy
stem and locus ceruleus ( 蓝斑)
Mechanisms:
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respiratory rate , tidal volume
occurs at ordinary doses, dose-related
the most common cause of death from acute
poisoning
Mechanisms:
the sensitivity of respiratory center to increased
CO2 tension
respiratory modulatory center
(3) Respiratory depression
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(4) Cough suppression
by inhibiting cough center directly
Has antitussive effectHas antitussive effect
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Miosis:
pinpoint pupils is characteristic of acute poisoning
blocked by naloxone and atropine
(5) Others
Nausea and vomiting:
activate the brain stem CTZ
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(5) Others• ↓release of gonadotropin-releasing hormone
(GnRH)
• ↓ release of corticotropin-releasing hormone
(CRF)
• ↓concentration of luteinizing hormone (LH) ,fol
licle-stimulating hormone(FSH)
• ↓adrenocorticotropic hormone(ACTH)
• ↑prolactin release
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Pharmacological actions
• 2. SM Stimulating
Gastrointestinal system
Biliary tract
Urinary
Bronchia
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(1) Gastrointestinal tract
delays passage
2. Smooth muscle system
secretion of digestive gland indigestion
central inhibition a call of nature
defecation reflex
sphincter tone
GIT tone GIT motility
absorption of water
constipationClinical uses?
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biliary colic
constrict biliary smooth muscle
constrict Oddi's sphincte
r
pressure in the biliary tract
(2) Biliary tract
Medicine?
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(3) Other smooth muscle
① constrict ureteral smooth muscle
constrict bladder sphincter
urinary retention
③ antagonize oxytocin ( 缩宫素) uterine tone
prolong labor
② constrict bronchial smooth muscle
bronchial asthma
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orthostatic hypotension
Mechanisms:
release of histamine
vasomotor center
3. Cardiovascular system
(1) peripheral arterial and venous dilatation
(2) intracranial pressure
secondary to respiratory depression
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4. Other actions
inhibit immune system
histamine release
bronchospasm
flushing
arteriolar dilatation
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1992~1993
1973
1962
1975
analgesic site is laminae III of periventricular and periaqueductal gray area
put forward “receptors” for opiate analgesics in brain
isolated the first “endogenous opioid peptide” and named enkephalin
cloned three opioid receptors: μ κ δ
Research on analgesic mechanisms
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Sites of analgesia
Supraspinal areas: thalamus, periventricular,
periaqueductal gray area
Spinal cord: substantia gelatinosa
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Opioid receptors
supraspinal analgesia, sedation, euphoria, respir
atory depression, miosis, dependence
spinal analgesia, sedation
dysphoria, hallucination
spinal analgesia, respiratory depression,
sedation, euphoria, dependence
**::
:
:
:
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Extracellular
Cytoplasmic
NH2
HOOC
Opioid receptors
G protein-coupled receptors
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Endogenous opioid peptides
Three main families:
Enkephalinsmet-enkephalin
leu-enkephalin
Endorphins: β-endorphine
Dynorphins: dynorphine A, B
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Mechanisms of analgesia
Supraspinal areas:
combined with receptors, activate desending i
nhibitory system
Spinal cord :
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Spinal cord
Dorsal hornenkephalins
Ca2+
Ca2+
谷氨酸
神经肽
Presynaptic terminal
Postsynaptic neuron
enkephalins
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enkephalins
Presynaptic terminal
Postsynaptic neuron
The cellular mechanisms of analgesia
morphine
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Presynaptic inhibition: activation of opioid receptors o
n presynaptic nerve terminals. Close a voltage-gated C
a2+ channel, decrease Ca2+ input, and thereby reduce t
ransmitter release.
The cellular mechanisms of analgesia
Postsynaptic inhibition: activation of postsynaptic opi
oid receptors. Open K+ channels on postsynaptic neur
ons, increase K+ output , and thereby cause hyperpola
rization and thus inhibit postsynaptic neurons.
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Clinical uses1.Analgesia
acute, severe pain, particularly in
terminal cancer
myocardial infarction
renal and biliary colic ( atropine)
short-term use only when others failed
2. *Cardiac asthma
3. Antidiarrhea
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Pulmonary edema
dyspnea
Acute left ventricular dysfunction
short of breath (respiratory center)
CO2 retention
anxiety and distress
Alveolar hypoventilation
morphine
Reduce cardiac preload and afterload
Reduce the sensitivity of the respiratory center to increased CO2
Sedation
Cardiac asthma and morphine therapy
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(1) Mechanisms:
① peripheral arterial and venous dilation
preload and afterload pulmonary edema
② sedation anxiety and distress
oxygen consumption
③ the sensitivity of respiratory center to CO2
shortness of breath
Cardiac asthma
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1. General adverse effects
1 dysphoria 5 Biliary colic
2Respiratory depression
6 Urinary retention
3Nausea and
vomiting7
Postural hypotension accentuated by hypovolemia
4 Constipation 8 Increased intracranial pressure
Adverse effects
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• Clinical overdose• Accidental poisoning in addicts• 30mg – toxic threshold• 120mg – lethal threshold
Pinpoint pupilsDeep respiratory depressionComa
Treatments: Establish patent airway Adequate ventilation Naloxone Iv.
The triad :
2. Acute Morphine Poisoning
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3. Tolerance and dependence(1) Tolerance a gradual loss in effectiveness in CNS with
frequently repeated administration, need larger
doses to achieve the same clinical effect.
Characteristic:
ordinary therapeutic doses 2-3 w
large doses at short intervals readily
develop not to miosis , constipation
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physical dependence : withdrawal syndrome
psychological denpendence:
euphoria promote compulsive use
and craving
(2) Dependence
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rhinorrhea lacrimation chills
gooseflesh (piloerection)
yawning sweating
muscular aches vomiting diarrhea
anxiety hostility hyperventilation
Withdrawalsyndrome of Opioid
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Contraindications
reasons that result in pain are not clear
obstetric labor, breasting period
cor pulmonale , bronchial asthma
head injuries
seriously impaired hepatic or renal function
newborn infant, infant
biliary and renal colic
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Codeine (methyl - morphine)
Characteristics:
1. has a higher1. has a higher oral efficacyefficacy
2. weaker analgesia, abouweaker analgesia, abou
t 1/10t 1/10 -- 1/121/12 , , antitussiveantitussive :: 1/41/4
3. used in moderate pain 3. used in moderate pain
4. maily use as antitussive, severe severe dry cough. cough.
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Pethidine (dolantin, meperidin)
analgesia: weaker(1/7-1/10) and shorter(2-4h)
sedation, euphoria, respiratory depression: equal
no antitussive action
1. Metabolisms
normeperidine muscle tremors, witches, convulsion
2. Pharmacological properties
(1) CNS
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(3) Cardiovascular system
similar to morphine
(2) smooth muscle
less constipation and urinary retention
do not prolong labor
may induce biliary colic
large doses
the contraction of bronchial smooth muscle
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3. Clinical uses
(1) Analgesia
obstetric labor
but should not be used in 2 - 4 h before labor
do not longtime use in chronic pain .
(2) Cardiac asthma
(3) Premedication in anesthesia
sedative, anxiolytic, and analgesia
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(4) Artificial hibernation
pethidine chlorpromazine promethazine
lytic cocktailⅠ4. Adverse effects(1) CNS excitatory symptoms
muscle tremors, twitches, convulsion should be combined with anticonvulsive drugs when treat overdose poisoning
(2) some symptoms like atropine
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Increased CNS depression, particularly respiratory depression
Opioid analgesics
MAOIs
Tricyclic antidepressants
chlorpromazine promethazine
Sedative- hypnotics
Absolute contraindication to pethidine , relative contraindication to other opioid analgesics , because of high incidence of hyperpyretic coma
Drug – Drug interactions
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MethadoneCharacteristics:
1. analgesia: equal to morphine
2. give reliable effects orally, longer duration of action
3. tolerance and physical dependence more slowly
4. withdrawal signs attenuated but protracted
5. detoxification of the morphine and heroin
dependent addict
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Fentanyl Characteristics: 1. more analgesic potentcy than morphine:100 times
2. has a rapid onset and short duration of action
3. high lipid- soluble, transdermal administration
4. + droperidol ( 氟哌利多) neuroleptanalgesia( 神经阻滞镇痛术) or usually combined with anaesthetics
5. high dose cause truncal rigidity
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Short acting
fentanyl sufentanil alfentanil
Agonistsmixed Agonists /Antagonists
Antagonists
WEAK: codeine pentazocine
STRONG:methadone morphine pethidine
buprenorphine nalbuphinelong
actingnaltrexone
naloxone
Classification of opioid analgesics
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Section 2 Partial agonists of opioid receptor
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PentazocineCharacteristic:
κ, σ agonist , μ weak antagonist
1. CNS
analgesia: 1/3
respiratory depression : 1/2
* psychomimetic action (60-90mg)
dysphoric and hallucination (action on σ)
2. Smooth muscle: weaker
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Pentazocine3. Cardiovascular systemCardiovascular system
high doses
*increase blood pressure and cause tachycardia
(catecholamine )
not use in myocardial infarction
4. weak action on μ * little addictive liability * precipitate the withdrawal syndrome of a morphine abuser 5. various chronic pain
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Section 4 Other analgesics
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Tramadol
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Section 5Antagonists of opioid receptors
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Naloxone
Characteristics:
1. competitive antagonist for opioid receptors:
potency μ κ δ﹥ ﹥ reverse the opioid effects
2. iv.
3. rapid onset (1~3 min), short duration of
action
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Naloxone
4. acute opioid poisoning : reverses the coma and respiratory depression
5. differential diagnosis in morphine or heroin
abuser : precipitates withdrawal symptom
6. As a tool agent in pharmacological research
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Three step analgesia Three step analgesia therapy for cancer patientstherapy for cancer patients
AppendixAppendix
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Non-opioid for mild pain
Pain persisting or increasing
Opioid for moderate pain
Pain persisting or increasing
Opioid for severe pain
Freedom from cancer pain
Pain
NSAIDs e.g. aspirin, acetaminophen
e.g. codeine , tramadol
e.g. morphine, pethidine
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病例:
张某 , 男 , 30 岁 , 因车祸伤导致左下肢疼痛不能活动送入急症科。查体发现基本生命体征平稳 , 病人痛苦貌 , 多处皮肤擦伤 , 左小腿前侧有一长约 20 厘米的皮肤裂伤 , 伴有骨折端外露 , 病人左上腹部亦有轻微疼痛感但较软无明显压痛。随即行双下肢 , 骨盆 x 线检查 , 提示左胫腓骨粉碎性骨折。病人检查过程中自觉腹部及小腿疼痛加剧 , 不能配合清创 , 于是值班医生给予度冷丁 50mg 肌肉注射 , 病人疼痛感减轻 , 并行简单清创后将病人推往手术室行骨折修复手术 . 问:这个给病人应用度冷丁合适么 ?
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病人转入手术室以后准备行手术治疗 , 麻醉前测量血压发现病人血压 80/50mmhg 睑结膜 ,
口唇苍白 , 四肢冷且苍白 , 骨外科主任医师立即详细询问急症值班医生有关处理后立即行腹腔穿刺 , 穿出大量不凝血性液体 . 立即给予快速多通道补液输血治疗 , 并请普外科医师会诊 , 考虑脾脏破裂 , 随即给予手术修补治疗 .
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