4.7 Article

Anti-Inflammatory and Analgesic Effects of Curcumin Nanoparticles Associated with Diclofenac Sodium in Experimental Acute Inflammation

Journal

Publisher

MDPI
DOI: 10.3390/ijms231911737

Keywords

curcumin; nanoparticles; diclofenac sodium; carrageenan; inflammation; cytokines

Funding

  1. Iuliu Hatieganu University of Medicine and Pharmacy Cluj-Napoca [PCD 1032/16/13]

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This study confirmed the significant anti-inflammatory and analgesic effects of conventional curcumin and curcumin nanoparticles combined with diclofenac sodium in acute inflammation. The combination treatment effectively reduced pain, improved mechanical pressure and heat thresholds, and decreased levels of inflammatory cytokines and histological changes. Overall, the combination of curcumin nanoparticles with diclofenac sodium showed the best results in reducing inflammation.
The present study evaluated the anti-inflammatory and analgesic effects of conventional curcumin (cC) and curcumin nanoparticles (nC) associated with diclofenac sodium (D) in experimental acute inflammation (AI) induced by carrageenan administration. Seven groups of eight randomly selected Wistar-Bratislava white rats were evaluated. One group was the control (C), and AI was induced in the other six groups. The AI group was treated with saline solution, the AID group was treated with D, the AIcC200 and AInC200 groups were treated with cC and nC, respectively, while AIcC200D and AInC200D were treated with cC and nC, respectively, both associated with D. Conventional curcumin, nC, and D were administered in a single dose of 200 mg/kg b.w. for cC and nC and 5 mg/kg b.w. for D. Association of cC or nC to D resulted in significant antinociceptive activity, and improved mechanical pressure stimulation and heat thresholds at 3, 5, 7 and 24 h (p < 0.03). The association of cC and nC with D (AIcC200D and AInC200D groups) showed significantly lower plasma and tissue levels of tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6), and interleukin-1 beta (IL-1 beta) up to 2.5 times, with the best results in the group who received nC. Moreover, AInC200D presented the least severe histopathological changes with a reduced level of inflammation in the dermis and hypodermis. The combination of nC to D showed efficiency in reducing pain, inflammatory cytokines, and histological changes in acute inflammation.

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