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Prostaglandins
D R . S U A L E H H A S S A N
P A T H O L O G Y D E P T .
A I M C
EICOSANOIDS
 Eicosanoids are metabolites of
arachidonic acid or other
unsaturated fatty acids derived
from the action of the
cyclooxygenase or lypoxygenase
enzymatic pathway
 Cyclooxygenase – prostanoids
 Lypoxygenase - leukotrienes
 Eicosanoids are classified into 2
main groups;
Cont…
1. Leukotrienes and lipoxins
2. Prostanoids
a) Prostaglandins (PGs)
b) Prostacyclins (PGI2)
c) Thromboxanes (TXs)
Cont…
 The key precursor fatty acid is arachidonic acid,
which is an essential fatty acid as it cannot be
synthesized de novo in animals
 The primary precursor is obtained from the diet in
the form of linoleic acid (polyunsaturated omega-6
fatty acid). It typically occurs in nature as a
triglyceride ester
Prostaglandins
 PGs are extremely potent, biologically active lipid
mediators that are synthesized throughout the body
 PGs have diverse hormone-like effects in animals
 They are derived enzymatically from the fatty acid
arachidonic acid
Biosynthesis of PGs
 Involves the action of multiple enzymes, some of
which are rate limiting
1. The first step is production of free arachidonic acid
from membrane phospholipids upon stimulation of
the enzyme phospholipase A2
2. The COX pathway, accomplished by catalytic
activity of two distinct cyclooxygenase (COX-1
and COX-2) isozymes encoded by separate genes
-produces PGG2 and then PGH2
Cont…
3. PGH2 is then converted into
-PGI2 by prostacyclin synthase
-TXA2 by thromboxane synthase, and
-PGE2, PGD2 and PGF2α by their respective synthase
enzymes
 PGs are produced in the endoplasmic reticulum, exit
the cell and signal through G protein-linked
receptors at the cell surface
COX-1 COX-2
 Constitutive
 Present in most tissues
 Synthesizes PGs that
regulate physiologic
processes
 Especially important in
-gastric mucosa
-kidneys
-platelets
-vascular endothelium
 Inducible
 Induced mainly at sites of
inflammation by cytokines
 Synthesizes PGs that
mediate inflammation,
pain, and fever
 Constitutive expression
primarily in
-brain
-kidneys
Differences between COX-1 and COX-2
Cont…
 Both COX iso-enzymes are inhibited by NSAIDs,
such as acetylsalicylic acid and ibuprofen
 This prevents synthesis of endogenous PGs
 Because of differences in the structures of the
binding sites, COX-1 is completely inhibited by
aspirin, whereas COX-2 is only partially inhibited
 Synthesis of COX-2 is inhibited by steroidal anti-
inflammatory drugs at the level of transcription
PG Receptors
 PGs function close to the site of synthesis and are
deactivated to inactive metabolites before moving
into the circulation
 They act locally in very low concentrations to
produce profound physiological changes through
receptor-mediated G-protein linked signaling
pathways
 The immediate effect of the appearance of PGs is a
change in the rate of production of second
messengers such as cAMP or Ca2+ and a change in
the activation of a specific protein kinase
Biological Functions of PGs
 Maintenance of IOP (Intraocular Pressure)
 Vasodilation/vasoconstriction
 Cause aggregation or disaggregation of platelets
 Regulate inflammation
 Induce labor
 Acts on parietal cells in the stomach wall to inhibit
acid secretion
 Increase glomerular filtration rate
 Sensitize spinal neurons to pain
Inhibitors of PGs
 NSAIDs (inhibit cyclooxygenase)
 Corticosteroids (inhibit phospholipase
A2 production); used in allergic reaction and to
relive inflammation
 COX-2 selective inhibitors or coxibs eg; Celecoxib,
used to treat arthritis pain and RA
Clinical use of synthetic PG analogs
 To induce labour or abortion
PGE1 analogue - misoprostol
PGE2 analogue - dinoprostol
PGF2 analogue – dinoprost
 To prevent closure of patent ductus arteriosus in
newborns with particular CHD (PGE1)
 As a vasodilator in severe Raynaud's
phenomenon or ischemia of a limb
Cont…
 In treatment of IOP and glaucoma, PGF2α analogs eg;
travoprost, latanoprost and bimatoprost
 In pulmonary hypertension
 To prevent and treat peptic ulcers (PGE)
 To treat erectile dysfunction or in penile
rehabilitation following surgery (PGE1
as alprostadil)
How PGs are different from true
hormones
 Are formed in almost all tissues rather than in
specialized glands
 Act locally rather than to distance sites
 Act on their parent cells
 Are not transported via blood
 Are synthesized as per needed
 Are not stored

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MBBS AIMC prostaglandins and uses and pharma.pptx

  • 1. Prostaglandins D R . S U A L E H H A S S A N P A T H O L O G Y D E P T . A I M C
  • 2. EICOSANOIDS  Eicosanoids are metabolites of arachidonic acid or other unsaturated fatty acids derived from the action of the cyclooxygenase or lypoxygenase enzymatic pathway  Cyclooxygenase – prostanoids  Lypoxygenase - leukotrienes  Eicosanoids are classified into 2 main groups;
  • 3. Cont… 1. Leukotrienes and lipoxins 2. Prostanoids a) Prostaglandins (PGs) b) Prostacyclins (PGI2) c) Thromboxanes (TXs)
  • 4. Cont…  The key precursor fatty acid is arachidonic acid, which is an essential fatty acid as it cannot be synthesized de novo in animals  The primary precursor is obtained from the diet in the form of linoleic acid (polyunsaturated omega-6 fatty acid). It typically occurs in nature as a triglyceride ester
  • 5. Prostaglandins  PGs are extremely potent, biologically active lipid mediators that are synthesized throughout the body  PGs have diverse hormone-like effects in animals  They are derived enzymatically from the fatty acid arachidonic acid
  • 6. Biosynthesis of PGs  Involves the action of multiple enzymes, some of which are rate limiting 1. The first step is production of free arachidonic acid from membrane phospholipids upon stimulation of the enzyme phospholipase A2 2. The COX pathway, accomplished by catalytic activity of two distinct cyclooxygenase (COX-1 and COX-2) isozymes encoded by separate genes -produces PGG2 and then PGH2
  • 7. Cont… 3. PGH2 is then converted into -PGI2 by prostacyclin synthase -TXA2 by thromboxane synthase, and -PGE2, PGD2 and PGF2α by their respective synthase enzymes  PGs are produced in the endoplasmic reticulum, exit the cell and signal through G protein-linked receptors at the cell surface
  • 8.
  • 9. COX-1 COX-2  Constitutive  Present in most tissues  Synthesizes PGs that regulate physiologic processes  Especially important in -gastric mucosa -kidneys -platelets -vascular endothelium  Inducible  Induced mainly at sites of inflammation by cytokines  Synthesizes PGs that mediate inflammation, pain, and fever  Constitutive expression primarily in -brain -kidneys Differences between COX-1 and COX-2
  • 10. Cont…  Both COX iso-enzymes are inhibited by NSAIDs, such as acetylsalicylic acid and ibuprofen  This prevents synthesis of endogenous PGs  Because of differences in the structures of the binding sites, COX-1 is completely inhibited by aspirin, whereas COX-2 is only partially inhibited  Synthesis of COX-2 is inhibited by steroidal anti- inflammatory drugs at the level of transcription
  • 11. PG Receptors  PGs function close to the site of synthesis and are deactivated to inactive metabolites before moving into the circulation  They act locally in very low concentrations to produce profound physiological changes through receptor-mediated G-protein linked signaling pathways  The immediate effect of the appearance of PGs is a change in the rate of production of second messengers such as cAMP or Ca2+ and a change in the activation of a specific protein kinase
  • 12. Biological Functions of PGs  Maintenance of IOP (Intraocular Pressure)  Vasodilation/vasoconstriction  Cause aggregation or disaggregation of platelets  Regulate inflammation  Induce labor  Acts on parietal cells in the stomach wall to inhibit acid secretion  Increase glomerular filtration rate  Sensitize spinal neurons to pain
  • 13.
  • 14. Inhibitors of PGs  NSAIDs (inhibit cyclooxygenase)  Corticosteroids (inhibit phospholipase A2 production); used in allergic reaction and to relive inflammation  COX-2 selective inhibitors or coxibs eg; Celecoxib, used to treat arthritis pain and RA
  • 15. Clinical use of synthetic PG analogs  To induce labour or abortion PGE1 analogue - misoprostol PGE2 analogue - dinoprostol PGF2 analogue – dinoprost  To prevent closure of patent ductus arteriosus in newborns with particular CHD (PGE1)  As a vasodilator in severe Raynaud's phenomenon or ischemia of a limb
  • 16. Cont…  In treatment of IOP and glaucoma, PGF2α analogs eg; travoprost, latanoprost and bimatoprost  In pulmonary hypertension  To prevent and treat peptic ulcers (PGE)  To treat erectile dysfunction or in penile rehabilitation following surgery (PGE1 as alprostadil)
  • 17. How PGs are different from true hormones  Are formed in almost all tissues rather than in specialized glands  Act locally rather than to distance sites  Act on their parent cells  Are not transported via blood  Are synthesized as per needed  Are not stored