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Chapter 32 drug used in digestive system

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Title: Chapter 32 drug used in digestive system


1
Chapter 32drug used in digestive system
2
  • This chapter describes drugs used to treat these
    common medical conditions involving the
    gastrointestinal tract
  • peptic ulcers, dyspepsia, vomitting, diarrhea and
    constipation, etc.

3
Part ? Drugs Used in Peptic Ulcer
4
peptic ulcer
  • A benign, localized defect in the mucosa of
    any part of the gastrointestinal tract.
  • duodenal ulcer
    gastric ulcer

5
Symptoms and complications
  • The most important symptom is abdominal pain and
    discomfort. The atypical symptoms are abdomen
    distention, inappetence, belching, reflux of
    gastric acid.
  • The severe complications are hemorrhage,
    perforation, obstruction and canceration.

6
Pathogenesis of peptic ulcer
  • although the pathogenesis of peptic ulcer disease
    is not fully understood,
  • the theory that the balance between mucosal
    defense and injury is broken are recognized.

7
  • Pathogenesis of peptic ulcer
  • 1. Aggressive factors?
  • Helicobacter Pylori ( H. Pylori)
  • gastric acid and pepsin
  • 2. Defensive factors?
  • mucus-bicarbonate barrier
  • prostaglandins

8
Helicobacter Pylori ( H. Pylori)
  • In 1983, H. pylori was found by two Australians,
    Marshall and Warren.
  • Now, it is believed that H. pylori is the most
    important pathogenic factor to peptic ulcer.
  • No H.P., no ulcer.
  • And the two men won the noble prize for the
    important findings in 2005.

9
H. Pylori (48,000)
10
H. Pylori on gastric mucosa(16,000)
11
Actions of H. Pylori
12
gastric acid and pepsin
  • Pepsin can decompose protein molecule. But its
    activity is depended on the pH value. When local
    pH value elevates to 4, pepsin cant work well.
  • Gastric acid is the key-factor of the formation
    of peptic ulcer. we can also say that No acid,
    no ulcer.

13
mucus-bicarbonate barrier
  • The epithelial layer of the mucosa is
    composed of tightly adjoined cells that are
    specialized for existence in an acid medium.
    Their tight junctions, synthesis of PGs and
    secretion of mucus and bicarbonate all contribute
    to maintenance of the epithelial barrier.

14
mucus-bicarbonate barrier
15
Prostaglandins(PGs)
  • Prostaglandins are thought to enhance resistance
    to injury by maintaining blood flow to the
    mucosa.
  • Thus it also plays a major role in the
    maintenance of defensive mechanism.

16
  • Classification of drugs
  • ?.Antacids
  • ?.Agents decreasing secretion of
  • gastric acid
  • ?. Agents protecting mucosal barrier
  • ?.Agents eradicating helicobacter
  • pylori

17
? Antacids
  • Have been used for centuries in the treatment of
    patients with acid-peptic disorders.
  • Were the mainstay of treatment for acid-peptic
    disorders until the advent of H2-receptor
    antagonists and proton pump inhibitors.

18
? Antacids
  • weak bases Mg(OH)2 , Al(OH)3 ,
  • CaCO3 , NaHCO3
  • actions
  • 1) prevent injury from H
  • 2) neutralize gastric acid ? reduce gastric
    acidity? reduce peptic activity
  • 3) protect face of ulcer( Mg2SiO8 Al(OH)3 )

19
  • ? Antacids
  • NaHCO3HCl ? NaclH2OCO2?
  • Mg2Si3O84HCl ? 2MgCl23SiO2
  • Al(OH)33HCl ? AlCl33H2O
  • Mg(OH)2HCl ? MgCl22H2O
  • CaCO32HCl ? CaCl2H2OCO2 ?
  • MgOHCl ? MgCl2H2O

20
  • ?1?????????????
  • NaHCO3 Mg2SiO8 Al(OH)3 Mg(OH)2
    CaCO3 MgO
  • 1g???0.1 120 150
    250 210 200 500
  • N?HCl ml?
  • ???? ?? ?? ???
    ??? ??? ??
  • ?????? ? ?
    ?? ?? ?? ??
  • ????? ? ?
    ? ? ? ?
  • ???? ? ?
    ? ? ? ?
  • ??CO2 ? ?
    ? ? ? ?
  • (??)
  • ???? ? ?
    ? ? ? ?
  • ???? ? ?
    ? ? ? ?
  • ????? ? ?
    ? ? ? ?

??
??
??
21
  • side reactions
  • disorder of gastrointestinal track
  • diarrhea constipation belching(??)
    flatulence (????)
  • alkalemia

22
? Agents reducing secretion of gastric acid
23
Regulation of gastric acid secretion
24
  • Drugs reducing secretion of gastric acid
  • (1) H2-receptor antagonists
  • (2) Antimuscarinic agents
  • (3) Inhibitors of the proton pump
  • (4) gastrin-receptor antagonists

25
H2-R antagonists
  • Cimetidine, Ranitidine, Famotidine , Nizatidine
  • Actions
  • Competitively block the binding of histamine
    to H2 receptor. Completely inhibit gastric
    acid secretion induced by histamine.
  • characteristics
  • more effective than M-R antagonistslong
    duration high rate of healing up rebound

26
Regulation of gastric acid secretion
27
Cimetidine(????????)
  • Pharmacokinetics
  • Absorption p.o F70
  • Distribution widely
  • Elimination kidney
  • ! Heptic microsomal enzyme inhibitor
  • Action
  • inhibit all kinds of gastric acid secretion

28
Clinical uses
  • ?peptic ulcers 
  • effective in promoting healing of peptic ulcers.
    400 mg bid 4W?80 healing
  • after treatment is stopped, recurrence is common.
    This can be effectively prevented by eradication
    of H.Pylori.

29
  • ?Zollinger-Ellison syndrome  a fatal disorder in
    which a gastrin-producing tumor causes
    hypersecretion of gastric acid.
  • In many patients, H2 receptor antagonists can
    effectively keep the acid secretion to safe
    levels so as to control symptoms related to
    excess acid secretion.

30
  • ?gastroesophageal reflux disorder
  • (GERD, heartburn)
  • Because they act through stopping acid secretion,
    they may not relieve symptoms of heartburn for at
    least 45 minutes.
  • Antacid will be more efficiently to neutralize
    secreted acid already in the stomach.

31
Adverse reactions
  • 1.the common side effects are
  • headache, dizziness, diarrhea and muscular
    pain, skin rash
  • 2.CNS effects
  • confusion, disorientation and hallucination
  • 3. Endocrine system effects gynecomastia,
    impotency, galactorrhea(??)

32
  • Ranitidine(????)
  • 1) Antisecretive effect is 10 times that
    of Cimetidine .
  • 2)Less effect on hepatic microsomal
    metabolism system.
  • 3)Longer duration and less
    antiandrogenic effect

33
  • Famotidine(????)
  • 1) Antisecretive effect is 40 times that of
    Cimetidine .
  • 2) Have no effect on hepatic microsomal
    metabolism system.
  • Nizatidine(????)
  • Ebrotidine(????)
  • 1) ?Expression of EGF and
    PDGF?stimulate proliferation of epithelium
  • 2) increase mucus secretion

34
Inhibitors of the proton pump
  • Omeprazole, lansoprazole, pantoprazole
  • pharmacological effects
  • Inhibits H being transported to gastric lumen
    through inhibiting the proton pump.
  • Potent and long-lasting effect Can inhibit over
    95 of gastric acid secretion.
  • Also inhibit release of peptin and H.P

35
Regulation of gastric acid secretion
36
Clinical uses
  • ?peptic ulcer was judged to be superior to
    H2-R antagonists
  • ?Zollinger-Ellison syndrome
  • ? heartburn the most effective agents.
  • ?hemorrhage of upper digestive tract
  • ? H.P infection

37
Adverse reactions extremely safe
  • 1)G.I reactions nausea,vomitting, diarrhea,
    abdominal pain etc.
  • 2)NS headache, swirl, insomnia, peripheral
    neuritis, etc.
  • 3) overgrowth of bacteria Increases in gastric
    bacterial concentrations.
  • 4)hypergastrinemia(??????)
  • 5)canceration

38
  • Omeprazole
  • Easily absorbed, but affected by food
  • Is also heptic enzyme inhibitor
  • lansoprazole second generation
  • Pantoprazole and rabeprazole
  • third generation
  • weak effect on heptic enzyme

39
Antimuscarinic agents
  • Muscarinic receptor stimulation increase
    gastrointestinal motility and secretion.
  • So cholinergic antagonists can be used as
    adjuncts in the management of peptic ulcer
    disease and Zollinger-Ellison syndrome,
    particularly in patients refractory to standard
    therapies.

40
Regulation of gastric acid secretion
41
Antimuscarinic agents
  • In contrast to the classic anticholinergics, the
    relatively specific M1-receptor antagonist,
    Pirenzepine is a good choice as an
    anti-secretory agent. Because it suppresses basal
    and stimulated gastric acid secretion at doses
    having a minimal effect on other organs (salivary
    glands, the heart and eye.)

42
  • gastrin-receptor antagonists
  • proglumide(???)

43
? Agents protecting mucosal barrier
  • (1)Prostaglandins
  • (2)Mucosal protective agents

44
  • Prostaglandins
  • prostaglandins E2 and I2, produced by the gastric
    mucosa, inhibit secretion of gastric acid and
    stimulate secretion of mucus and bicarbonate
    (cytoprotective effect) .
  • A deficiency of prostaglandins is thought to be
    involved in the pathogenesis of peptic ulcers.

45
Mucosal protective agents
  • These compounds, known as cytoprotective ones ,
    have several actions that enhance mucosal
    protection mechanisms, thereby preventing mucosal
    injury, reducing inflammation and healing
    existing ulcers.
  • clinical uses NSAID-induced ulcer
  • adverse reactions dose-dependent diarrhea,
    stimulate uterus

46
Misoprostol a stable analog of PGE2
  • (1) inhibits secretion of gastric acid and
    stimulate secretion of mucus and bicarbonate.
  • (2) dilate blood vessel of mucous membrane.
  • (3) currently the only agent approved for
    prevention of gastric ulcers induced by NSAIDs.
  • (4)less effective than H2-receptor antagonists
    for acute treatment of peptic ulcers.
  • (5)produces uterine contractions and is
    contraindicated during pregnancy.

47
Mucosal protective agents
  • Sucralfate(???)
  • 1)In water or acidic solutions it forms a
    viscous, tenacious paste that binds selectively
    to ulcers or erosions for up to 6 hours.
  • 2)Also stimulates prostaglandin release and mucus
    and bicarbonate output.
  • 3)Promote effects of growth factors
  • 4)Inhibit H.P
  • ! Needs acid envioment affects absorption of
    other drugs

48
Mucosal protective agents
  • colloidal bismuth subcitrate (?????)
  • 1) binds to an ulcer crater, coating it and
    protecting it from acid and pepsin.
  • 2) Inhibits the activity of pepsin
  • 3) increases mucous secretion
  • 4) increase prostaglandin synthesis
  • 5) helps to eradicate H. pylori

49
Antimicrobial agents
  • Optimal therapy of patients with peptic ulcer
    disease who are infected with H.Pylori requires
    antimicrobial treatment.
  • Eradication of H.Pylori results in rapid healing
    of active peptic ulcers and low recurrence rates.
  • Metronidazole, tetracycline, amoxiciliin, etc.
  • Often combined with other drugs.

50
  • Section 2
  • Drugs modulating digestive function
  • ? Digestants
  • Dilute hydrochloric acid
  • Pepsin
  • Pancretin
  • biofermin

51
? Antiemetic and prokinetic agents
52
  • ? Antiemetic and prokinetic agents
  • ? Antiemetic agents
  • 1. H1-receptor antagonist
  • Dimenhydrinate (???)
  • 2. M-receptor antagonist
  • scopolamine

53
3. dopamine antagonists
  • Metoclopramide(?????)
  • mechanism
  • 1) block D2-receptor in CTZ ? antinausea and
    antiemetic action
  • 2) block gastrointestinal D2-receptor
  • ? promote vermiculation(???)

54
  • Clinical use
  • prevention of vomitting
  • gastrointestinal reflux disease
  • nonulcer dyspepsia
  • impaired gastric emptying
  • adverse reaction
  • extrapyramidal symptoms,
  • especially dystonias(????)

55
  • Domeperidone (????)
  • block gastrointestinal D2-receptor
  • ? promote vermiculation
  • Cisapride(????)
  • DA, Ach, 5-HT

56
  • 4. 5-HT3 inhibitor
  • ondansetron
  • used in the prevention of chemotherapy-induced
    and postoperative nausea and vomiting
  • Granisetron(????)
  • Tropisetron(????)

57
  • ? Antidiarrheal agents
  • Increased motility of the gastrointestinal
    tract and decreased absorption of fluid are major
    factors in diarrhea.
  • So antidiarrheals include anti-motility agents,
    adsorbents and drugs that modify fluid and salt
    transport.

58
  • 1.Opium receptor agonists
  • Opium tincture
  • Tincture camphor compound
  • Diphenoxylate (????)
  • Loperamide(????)

59
  • Diphenoxylate(????)
  • Opioids are the most effective agents for relief
    of diarrhea.
  • Is an analog of pethidine and have opioid-like
    actions on the gut.
  • block gastrointestinal µ-receptor ? decrease
    vermiculation(???)
  • Is used to control acute or chronic functional
    diarrhea
  • difficultly penetrate BBB, have no extrapyramidal
    symptoms

60
  • 2.Astringents(???)
  • Tannalbin(????)
  • 3.Absorbants
  • Medical charcoal, Smectite(???),kaolin ,
    and pectin
  • They act as absorbents of bacteria,
    toxins, and fluid, thereby decreasing stool
    liquidity and quantity. They may be useful in
    acute diarrhea but are seldom used on a chronic
    basis.

61
  • ? Laxatives(??)
  • 1.Contact laxatives
  • Phenolphthalein(??), Bisacodyl(????)
  • Anthraquinones(??) rhubarb(??).senna(???)
  • 2.Osmotic laxatives
  • Magnesium sulfate

62
  • Machanism
  • form gels in the large intestine, causing
    water retention and intestinal distension,
    thereby increasing motility.
  • Effects and uses
  • (1)Diarrhea
  • (2) Cholagogic(???) action
  • (3) Relax skeletal muscles
  • (4)Relax vascular smooth muscle

63
  • Sodium sulfate, Lactulose(???), Glycerol
    (??), castor oil(???) , celluloses(???)
  • 3. Stool softeners
  • Liquid paraffin(??)
  • ? Choleretics (learn by yourself)

64
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