The use of Stronger Neo-Minophagen C, a glycyrrhizin-containing preparation, in robust neuroprotection in the postischemic brain.
10.5115/acb.2011.44.4.304
- Author:
Seung Woo KIM
1
;
Chae Moon LIM
;
Hye Kyung LEE
;
Ja Kyeong LEE
Author Information
1. Department of Anatomy, Center for Advanced Medical Education by BK21 Project, Inha University School of Medicine, Incheon, Korea. jklee@inha.ac.kr
- Publication Type:Original Article
- Keywords:
Glycyrrhizic acid;
Stronger Neo-Minophagen C;
Middle cerebral artery infarction;
Neuroprotection;
Anti-inflammation
- MeSH:
Animals;
Brain;
Cell Line;
China;
Cysteine;
Drug Combinations;
Glycine;
Glycyrrhetinic Acid;
Glycyrrhiza;
Glycyrrhizic Acid;
Humans;
India;
Infarction, Middle Cerebral Artery;
Japan;
Korea;
Liver Diseases;
Microglia;
Neuroprotective Agents;
Neutrophil Infiltration;
Rats;
Rhizome;
Taiwan
- From:Anatomy & Cell Biology
2011;44(4):304-313
- CountryRepublic of Korea
- Language:English
-
Abstract:
Stronger Neo-Minophagen C (SNMC) is a glycyrrhizin-containing preparation that is approved in Japan for the treatment of chronic hepatic diseases and is marketed in Japan, China, Korea, Taiwan, and India. Glycyrrhizin, a triterpene present in the roots and rhizomes of licorice (Glycyrrhiza glabra) has been shown to have anti-inflammatory, anti-oxidative, and anti-viral effects. In the present study, we demonstrated the marked neuroprotective effects of SNMC in the postischemic rat brain after middle cerebral artery occlusion (MCAO). We used 1 ml/kg of SNMC, which is within the dose range used for the treatment of patients with chronic hepatic disease. The administration of SNMC intravenously at 30 minutes before or 30 minutes and 3 hours after MCAO (60 minutes) reduces mean infarct volumes to 27.0+/-4.2%, 37.1+/-12.4%, and 67.8+/-5.8% of that of untreated controls, respectively. This neuroprotective effect is accompanied by improvements in motor impairment and neurological deficits. The administration of SNMC is shown to suppress microglia activation and neutrophil infiltration in the postischemic brain. In addition, SNMC suppresses lipopolysaccharide-induced nitrite production and proinflammatory cytokine induction in a microglia cell line, BV2. This indicates that the neuroprotective effect of SNMC might be due, at least in part, to an anti-inflammatiory effect. Interestingly, SNMC shows significantly higher neuroprotective potency compared to an equivalent dose of pure glycyrrhizin, in terms of reducing infarct volume and improving neurological deficits. Together these results indicate that SNMC, a glycyrrhizin-containing preparation developed for chronic liver disease, has a marked neuroprotective function in the postischemic brain via its anti-inflammatory effects.
