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Cyclooxygenases: From Prostaglandin Synthesis to Innovative Therapies for Inflammation
Sumeet Sharma1, Prerna Sharma2, Nidhi Rani3
1Pharmaceutical Sciences Department, ICFAI University, Baddi, Himachal Pradesh, India.
Non-steroidal anti-inflammatory drugs (NSAIDs) have serious side effects. New research focuses on safer cyclooxygenase-2 (COX-2) inhibitors, including natural supplements, for treating inflammatory diseases.
Area of Science:
- Biochemistry
- Pharmacology
- Oral Medicine
Background:
- Cyclooxygenases (COX) are key enzymes in prostaglandin synthesis, crucial for inflammation.
- Non-steroidal anti-inflammatory drugs (NSAIDs) are common but have significant side effects, leading to market withdrawals.
- Selective COX-2 inhibitors are sought for safer anti-inflammatory therapies.
Purpose of the Study:
- To review diseases linked to cyclooxygenase enzyme malfunction.
- To examine current therapies and explore novel drug discovery avenues for COX inhibition.
- To analyze pharmaceutical products for COX inhibition efficacy and side effects.
Main Methods:
- Literature review of cyclooxygenase enzyme function and related diseases.
- Analysis of current therapeutic strategies, including NSAIDs and newer inhibitors.
- Evaluation of pharmaceutical products targeting COX enzymes, considering history, efficacy, and safety profiles.
Main Results:
- NSAIDs, while effective, are associated with severe adverse effects.
- Cyclooxygenase enzymes are implicated in various physiological and pathological processes, including oral tissue disorders like periodontitis, pulpitis, and oral cancer.
- Emerging COX inhibitors, including dietary changes and natural supplements, show potential for improved safety and efficacy.
Conclusions:
- Cyclooxygenase enzyme malfunction underlies numerous diseases, necessitating safer therapeutic interventions.
- Current NSAIDs pose significant risks, driving the need for alternative treatments.
- Natural compounds and dietary modifications represent promising avenues for developing safer and more effective COX inhibitors.
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