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http://dx.doi.org/10.11625/KJOA.2014.22.3.469

Biological Evaluation of Nargenicin and Its Derivatives as Antimicrobial Anti-inflammatory Agents  

Cho, Seung-Sik (목포대학교 약학대학 천연약물연구소)
Hong, Joon-Hee (조선대학교 약학과)
Chae, Jung-Il (전북대학교 치의학대학원 치과약리학교실(BK21 플러스사업단))
Shim, Jung-Hyun (목포대학교 약학대학 천연약물연구소)
Na, Chong-Sam (전북대학교 동물생명공학과)
Yoo, Jin-Cheol (조선대학교 약학과)
Publication Information
Korean Journal of Organic Agriculture / v.22, no.3, 2014 , pp. 469-481 More about this Journal
Abstract
IIn vitro antimicrobial and anti-inflammatory activities of nargenicin and its derivatives were investigated. Nargenicin, an unusual macrolide antibiotic with potent anti-MRSA (methicilin-resistant Staphylococcus aureus) activity, was purified from the culture broth of Nocardia sp. CS682. And variety of novel nargenicin derivatives was synthesized from nargenicin. Two compounds (4 and 5) exhibit a broad spectrum of antimicrobial activities against infectious bacteria. The antimicrobial activity of derivatives against fifteen organisms was assessed using the minimum inhibitory concentration (MIC). The MIC values were in the ranges of $0.15{\sim}80{\mu}g/mL$ (w/v) for compound 1 and 2, $5{\sim}80{\mu}g/mL$ (w/v) for compound 3, $1.25{\sim}40{\mu}g/mL$ (w/v) for compound 4, and $1.25{\sim}80{\mu}g/mL$ (w/v) for compound 5, depending on the pathogens studied. In vitro, we investigated cytotoxicity and inhibition of nitric oxide (NO) production of synthesized compounds 1-5 in Raw 264.7 cells. LPS-induced nitric oxide releases were significantly blocked by compound 3, 4 and 5 in a dose-dependent manner. At high concentrations ($5{\mu}g/mL$) compound 5 inhibited the NO production by 95%. Compound 4 inhibited the release of NO in LPS-activated Raw 264.7 cells by 75% at the concentration of $10{\mu}g/mL$. Compound 3 inhibited the release of NO in LPS-activated Raw 264.7 cells by 65% at the concentration of $100{\mu}g/mL$. On the other hand, nargenicin, compound 1 and 2 did not inhibit NO production. These results demonstrated that compound 4 and 5 displayed antimicrobial activity and blocked LPS-induced pro-inflammatory mediators such as NO in macrophages, which might be responsible for its therapeutic application.
Keywords
nargenicin; nargenicin derivatives; antimicrobial activity; anti-inflammatory activity;
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