Description
Loxoprofen is a nonselective inhibitor of COX-1 and COX-2 that exhibits properties typical of most non-steroidal anti-inflammatory drugs (NSAIDs), including anti-inflammatory, analgesic, and antinociceptive activities. In vivo, loxoprofen decreases noxious heat-evoked neural responses. In other models, loxoprofen decreases levels of thromboxane B2 (TxB2) and prostaglandins E2 (PGE2) and F1 (PGF1), decreasing aortic atherosclerotic lesions. Additionally, loxoprofen decreases nocturia in subjects with benign prostatic hyperplasia (BPH) by increasing bladder capacity.
References
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Hamaguchi M, Seno T, Yamamoto A, et al. Loxoprofen Sodium, a Non-Selective NSAID, Reduces Atherosclerosis in Mice by Reducing Inflammation. J Clin Biochem Nutr. 2010 Sep;47(2):138-47. PMID: 20838569.
Araki T, Yokoyama T, Araki M, et al. A clinical investigation of the mechanism of loxoprofen, a non-steroidal anti-inflammatory drug, for patients with nocturia. Acta Med Okayama. 2008 Dec;62(6):373-8. PMID: 19122682.
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Sugimoto M, Kojima T, Asami M, et al. Inhibition of prostaglandin production in the inflammatory tissue by loxoprofen-Na, an anti-inflammatory prodrug. Biochem Pharmacol. 1991 Nov 27;42(12):2363-8. PMID: 1764120.