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Printable Handouts
Navigable Slide Index
- Introduction
- Pathology of COPD
- Air trapping in COPD
- New bronchodilators
- Human small airways: beta2-agonists
- Indacterol vs. salmeterol in COPD
- LABA+LAMA combination in COPD
- Unmet needs in COPD
- Cellular mechanisms of COPD
- Treating inflammation in COPD
- Anti-TNF-alpha in COPD
- Chemokine receptor antagonists in COPD
- CXCR2 antagonist in COPD
- Elastase activity of macrophages in COPD
- Effect of MMP9 inhibitor on emphysema
- Broad spectrum anti-inflammatory treatment
- PDE4 inhibitors in COPD
- Effect of roflumilast in COPD
- PDE4 inhibitors: side effects
- Inhaled PDE inhibitors for COPD
- p38 MAP kinase inhibitors
- p38 MAP kinase inhibitors in COPD
- Major barrier to effective treatment of COPD
- Amplification and steroid resistance
- Corticosteroids resistance in COPD
- Theophylline as HDAC activator
- How does theophylline restore HDAC?
- Reversal of corticosteroid resistance
- Nrf2 and antioxidant gene regulation
- Sulforaphane increases HDAC2 activity
- New drugs for COPD
Topics Covered
- New treatments for COPD include long-acting bronchodilators and combinations
- Mediator antagonists, including chemokine antagonists
- Broad-spectrum anti-inflammatory treatments
- Reversal of corticosteroid resistance by increasing HDAC2
Links
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Talk Citation
Barnes, P. (2012, July 31). New pharmacological therapies for COPD [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 27, 2024, from https://doi.org/10.69645/YJZL7901.Export Citation (RIS)
Publication History
Financial Disclosures
- Peter Barnes receives research grants from AstraZeneca and Boehringer-Ingelheim and is an advisor and/or gives talks for AstraZeneca, Boehringer-Ingelheim, Covis, Novartis, Pieris and Teva.