Pharmacology of inflammation Flashcards

1
Q

What drugs are included in the pharmacology of inflammation?

A

Aspirin and other NSAIDs
Steroids
Anti-inflammatory histamine antagonists (H1 blockers)

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2
Q

What do NSAIDs do?

A

act by irreversibly inhibiting COX enzymes (COX-1 and COX-2), leading to reduced prostanoid
synthesis, which has a number of anti-inflammatory effects:
1. Reduced vasodilation in response to prostaglandins PGE 2 and PGI 2 (prostacyclin) – as a result, there
is less oedema and swelling (probably main effect in headache)
2. Reduced sensitisation of nociceptive nerve endings to 5-HT and bradykinin
3. Reduced fever

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3
Q

What is aspirin?

A

A non-specific COX inhibitor

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4
Q

Adverse effects of aspirin

A

Major side effects of NSAIDs is gastric-bleeding due to a dual assault on the GI tract:
- Direct irritation of gastric mucosa by acidic molecules
- Loss of the protective effect of prostaglandins in the stomach due to COX-1 inhibition, resulting in
increased gastric acid secretion, reduced gastric blood flow and reduced mucus secretion

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5
Q

Is paracetamol an NSAID?

A

Its an analgesic but not an anti-inflammatory

Inhibits a specific COX and has analgesic and antipyretic effects on

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6
Q

What is the effect of steroids?

A

anti-inflammatory effect, primarily through inhibition of
transcription of the gene for IL-2 required for cloning of Th2 cells crucial to the inflammatory response
- In addition, they inhibit transcription of other inflammatory cytokines, including TNFa, IL-1, and IFN-gamma, as well as the expression of inducible inflammatory enzymes, such as phospholipase A2 (and
consequently leukotrienes, prostaglandins and platelet-activating factor, PAF), COX-2 , and inducible
nitric oxide synthase (iNOS)

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7
Q

Example of steroid

A

Dexamethasone

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8
Q

What are steroids used in?

A

Allergic conditons, including asthma

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9
Q

Adverse effects of steroids

A
  1. Immune depression, increasing susceptibility to viral infection
  2. Hypertension via effects on fluid and electrolyte balance
  3. Bone resorption, diabetes, peptic ulcers, effects on the skin
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10
Q

What is ca2+-mediated histamine release from mast cells partly responsible for?

A

The first two elements of the so-called ‘triple response’ to a mild insult to the skin:

  • the reddening due to arteriolar vasodilation
  • the wheal due to increased permeability of venules
  • (the ‘flare’ in surrounding tissue is due to release of vasodilators such as CGRP from nerve ending of sensory nerves in the vicinity of the insult)
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11
Q

Example of antihistamine

A

Chlorpheniramine

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12
Q

Downsides of antihistamines

A

non-specific effects, through inhibition of muscarinic, 5-HT, and -
adrenoreceptors – these effect contribute to drowsiness (but may be prescribed for motion sickness of
sedation)

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13
Q

What does treatment for RA typically involve?

A

Generally involves multiple anti-inflammatory and immunosuppressive drug therapy, combined with
analgesia to help with pain associated:

 Aspirin and other NSAIDs – reduce both pain and stiffness; but no effect on long-term disease
 Corticosteroids can be used – can be used short-term for flare-ups, while waiting for slow-onset
drugs to take effect; can be directly injected into joint (but long-term = osteoporosis)

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14
Q

What are DMARDS?

A

Disease modifying anti-rheumatic drugs - the primary treatment of RA

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15
Q

What do DMARDs do?

A

Depress the immune system over time (full effect takes over several months)

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16
Q

What drugs are considered DMARDs?

A

DONT NEED TO LEARN ALL OF THESE, JUST HAVE A LOOK AT EFFECTS
- methotrexate (most commonly used, usually first line treatment) – purine metabolism inhibitor
-hydroxychloroquine, sulfasalazine – suppress IL-1 and TNF-alpha, induce apoptosis of inflammatory
cells and decrease chemotaxis
- leflunomide – pyrimidine synthesis inhibitor
- certolizumab, infliximab – TNF-alpha inhibitors
- etanercept – TNF-alpha decoy receptor
-Abatacept – T-cell costimulatory signal inhibitor
- Rituximab andtocilizumab– monoclonal antibodies