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EICOSANOIDS IN SKIN
INFLAMMATION
Dr.Chandan Patil
I MVSc V 1661/16
Vety Pharmacology & Toxicology
DUVASU Mathura
INTRODUCTION
• Eicosanoids are major group of lipid –derieved
autacoids.
• Primarily derieved from Arachidonic acid
• Contribute to number of physiological and
pathological processes I,e homeoststic processes
and inflammatory responces.
• Eiconoid group includes
Prostaglandins,Thromboxanes,Leukotriens etc,
Cutaneous Eicosanoids
Biosynthesis
Cycloxygenase derieved mediators
• PGE2 is the main Cutaneous Eicosanoid
produced by epidermal keratinocytes & dermal
fibroblasts.
• PGE2 involvedin Keratinocyte proliferation
differentiation & modulation of dermal
fibroblasts and facilitate in wound healing.
• PGE2 has direct effect on melanocyte mediated
post inflamatory pigmentary response.
Cycloxygenase derieved mediators cont…
• Cutaneous PGD2 are produced by Langerhans
cells and Dermal mast cells
• Cutaneous PGD2 is a potent anti-proliferative
and anti-inflammatory PG
• PGD2 is precussor to the anti-inflammatory
cyclopentanone prostaglandins:PGJ2 that are
formed through non enzymatic hydrolysis.
Lipoxygenase derieved mediators
• Skin express 5-,8-,12-,15-LOX activity to produce
Hydroxyeicosatetraenoic acid(HETE) from fatty
acid derivatives of AA, Linoleic acid etc.
• 12HETE is potent pro-inflammatory chemotactic
mediator produced by epidermal keratinocytes &
dermal fibroblasts.
• 12 HETE binding sites are expressed by
keratinocytes and langerhans cells suggesting
active involvement in cutaneous wound healing
and inflammatory diseases.
Mechanism Of action
• All Prostanoid receptors are G-Protein
Coupled receptors.
• These prostanoids utilise IP3/DAG/CAMP
transducer mechanism to act on their receptors
Eicosanoids in cutaneous
inflammatory diseases
Atopic Dermatitis
Psoropsis Sunburn
Psoriasis
• Chronic inflammatory & proliferative skin
disease with genetic and environmental
etiologies characterised by abnormalities in
skin lipids and increased production of
inflammatory mediators
• Studies shown there is increased PLA2 activity
& high concentration of 12-HETE which is a
potent chemotactic eicosanoid highly prevalent
in psoriatic skin.
Psoriasis cont…
• On repeated injection of 15-HETE synthesised
by 15-LOX on the Psoriactic plaques resulted
in regression and complete resolution of
psoriasis
• So there has been interest in developing
specific 12-LOX & PLA2 inhibitors as
theraupetic agents to treat psoriasis
Atopic Dermatitis
• Characterised by increased PLA2 activity with
COX derieved prostanoids mediators.
• PGD2 is the principle prostanoid involved
because of active role of langerhans cells and
mast cells.
• Invitro studies with GLA and DHA suggested
PUFA can alter eicosanoids produced by
immune cells which helps in treating atopic
dermatitis
Sunburn Responce
• Characterised by increased COX and LOX
mediated eicosanoid production
• UVR induced oxidative stress stimulates
activity of PLA2 in human and animal skin
Effect of PUFA in Cutaneous
inflammation
• Long chain n-3PUFA effect eicosanoid production
through their ability to offer alternative substrates to
lipid metabolizing enzymes.
• Fish derieved omega-3 fatty acid
EPA(eicosapentaenoic acid) on action by COX
produce PGE3 which is less inflammaory & 12 lox
product such as 12-HEPE is less potent
chemoattractant than their Arachidonic acid
counterpart
• EPA also inhibit s COX2 expression in many cell
types .
References
• Eicosanoids in skin inflammation review article by Anna Nicolaou from
www.elsevier.com/plefa
• REDUCING INFLAMMATION WITH DIET AND SUPPLEMENTS:The Story of
Eicosanoid Inhibition general review by Subhuti Dharmananda, Ph.D.,
Director, Institute for Traditional Medicine, Portland, Oregon
Eicosanoids in skin inflammation

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Eicosanoids in skin inflammation

  • 1. EICOSANOIDS IN SKIN INFLAMMATION Dr.Chandan Patil I MVSc V 1661/16 Vety Pharmacology & Toxicology DUVASU Mathura
  • 2. INTRODUCTION • Eicosanoids are major group of lipid –derieved autacoids. • Primarily derieved from Arachidonic acid • Contribute to number of physiological and pathological processes I,e homeoststic processes and inflammatory responces. • Eiconoid group includes Prostaglandins,Thromboxanes,Leukotriens etc,
  • 4. Cycloxygenase derieved mediators • PGE2 is the main Cutaneous Eicosanoid produced by epidermal keratinocytes & dermal fibroblasts. • PGE2 involvedin Keratinocyte proliferation differentiation & modulation of dermal fibroblasts and facilitate in wound healing. • PGE2 has direct effect on melanocyte mediated post inflamatory pigmentary response.
  • 5. Cycloxygenase derieved mediators cont… • Cutaneous PGD2 are produced by Langerhans cells and Dermal mast cells • Cutaneous PGD2 is a potent anti-proliferative and anti-inflammatory PG • PGD2 is precussor to the anti-inflammatory cyclopentanone prostaglandins:PGJ2 that are formed through non enzymatic hydrolysis.
  • 6. Lipoxygenase derieved mediators • Skin express 5-,8-,12-,15-LOX activity to produce Hydroxyeicosatetraenoic acid(HETE) from fatty acid derivatives of AA, Linoleic acid etc. • 12HETE is potent pro-inflammatory chemotactic mediator produced by epidermal keratinocytes & dermal fibroblasts. • 12 HETE binding sites are expressed by keratinocytes and langerhans cells suggesting active involvement in cutaneous wound healing and inflammatory diseases.
  • 7. Mechanism Of action • All Prostanoid receptors are G-Protein Coupled receptors. • These prostanoids utilise IP3/DAG/CAMP transducer mechanism to act on their receptors
  • 8. Eicosanoids in cutaneous inflammatory diseases Atopic Dermatitis Psoropsis Sunburn
  • 9. Psoriasis • Chronic inflammatory & proliferative skin disease with genetic and environmental etiologies characterised by abnormalities in skin lipids and increased production of inflammatory mediators • Studies shown there is increased PLA2 activity & high concentration of 12-HETE which is a potent chemotactic eicosanoid highly prevalent in psoriatic skin.
  • 10. Psoriasis cont… • On repeated injection of 15-HETE synthesised by 15-LOX on the Psoriactic plaques resulted in regression and complete resolution of psoriasis • So there has been interest in developing specific 12-LOX & PLA2 inhibitors as theraupetic agents to treat psoriasis
  • 11. Atopic Dermatitis • Characterised by increased PLA2 activity with COX derieved prostanoids mediators. • PGD2 is the principle prostanoid involved because of active role of langerhans cells and mast cells. • Invitro studies with GLA and DHA suggested PUFA can alter eicosanoids produced by immune cells which helps in treating atopic dermatitis
  • 12. Sunburn Responce • Characterised by increased COX and LOX mediated eicosanoid production • UVR induced oxidative stress stimulates activity of PLA2 in human and animal skin
  • 13. Effect of PUFA in Cutaneous inflammation • Long chain n-3PUFA effect eicosanoid production through their ability to offer alternative substrates to lipid metabolizing enzymes. • Fish derieved omega-3 fatty acid EPA(eicosapentaenoic acid) on action by COX produce PGE3 which is less inflammaory & 12 lox product such as 12-HEPE is less potent chemoattractant than their Arachidonic acid counterpart • EPA also inhibit s COX2 expression in many cell types .
  • 14.
  • 15. References • Eicosanoids in skin inflammation review article by Anna Nicolaou from www.elsevier.com/plefa • REDUCING INFLAMMATION WITH DIET AND SUPPLEMENTS:The Story of Eicosanoid Inhibition general review by Subhuti Dharmananda, Ph.D., Director, Institute for Traditional Medicine, Portland, Oregon