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Published on: February 12, 2019
Recent Advances (2015-2020) in Drug Discovery for Attenuation of Pulmonary Fibrosis and COPD
Atukuri Dorababu1, Manikantha Maraswami2
1Department of Chemistry, SRMPP Government First Grade College, Huvinahadagali 583219, India.
Abstract:
A condition of scarring of lung tissue due to a wide range of causes (such as environmental pollution, cigarette smoking (CS), lung diseases, some medications, etc.) has been reported as pulmonary fibrosis (PF). This has become a serious problem all over the world due to the lack of efficient drugs for treatment or cure. To date, no drug has been designed that could inhibit fibrosis. However, few medications have been reported to reduce the rate of fibrosis. Meanwhile, ongoing research indicates pulmonary fibrosis can be treated in its initial stages when symptoms are mild. Here, an attempt is made to summarize the recent studies on the effects of various chemical drugs that attenuate PF and increase patients' quality of life. The review is classified based on the nature of the drug molecules, e.g., natural/biomolecule-based, synthetic-molecule-based PF inhibitors, etc. Here, the mechanisms through which the drug molecules attenuate PF are discussed. It is shown that inhibitory molecules can significantly decrease the TGF-β1, profibrotic factors, proteins responsible for inflammation, pro-fibrogenic cytokines, etc., thereby ameliorating the progress of PF. This review may be useful in designing better drugs that could reduce the fibrosis process drastically or even cure the disease to some extent.
Insights
Pulmonary fibrosis (PF) is lung scarring with no cure, but early treatment can help. This review explores drugs that slow fibrosis by reducing inflammation and profibrotic factors, potentially improving patient outcomes.
Area of Science:
- Pulmonary Medicine
- Pharmacology
- Biochemistry
Background:
- Pulmonary fibrosis (PF) is lung tissue scarring from diverse causes like pollution and smoking.
- The lack of effective treatments makes PF a global health concern.
- Current medications can only slow fibrosis progression, not inhibit or cure it.
Purpose of the Study:
- To review recent studies on chemical drugs that attenuate pulmonary fibrosis.
- To classify drugs based on their molecular nature (natural/biomolecule-based, synthetic-molecule-based).
- To discuss the mechanisms by which these drugs ameliorate PF and improve patient quality of life.
Main Methods:
- Literature review of recent studies on pulmonary fibrosis treatments.
- Classification of antifibrotic drugs by molecular origin.
- Analysis of drug mechanisms targeting profibrotic pathways.
Main Results:
- Various chemical drugs can attenuate pulmonary fibrosis.
- Inhibitory molecules reduce key profibrotic factors like TGF-β1, inflammation proteins, and cytokines.
- Drug efficacy is linked to their molecular class and mechanism of action.
Conclusions:
- Early-stage pulmonary fibrosis shows potential for treatment.
- Understanding drug mechanisms can guide the development of more effective antifibrotic therapies.
- Further research may lead to drugs that significantly reduce or cure pulmonary fibrosis.
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