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KCHO-1, a novel herbal anti-inflammatory compound, attenuates oxidative stress in an animal model of amyotrophic lateral sclerosis.
- Source :
-
Journal of veterinary science [J Vet Sci] 2017 Dec 31; Vol. 18 (4), pp. 487-497. - Publication Year :
- 2017
-
Abstract
- Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by selective death of motor neurons in the central nervous system. The main cause of the disease remains elusive, but several mutations have been associated with the disease process. In particular, mutant superoxide dismutase 1 (SOD1) protein causes oxidative stress by activating glia cells and contributes to motor neuron degeneration. KCHO-1, a novel herbal combination compound, contains 30% ethanol and the extracts of nine herbs that have been commonly used in traditional medicine to prevent fatigue or inflammation. In this study, we investigated whether KCHO-1 administration could reduce oxidative stress in an ALS model. KCHO-1 administered to ALS model mice improved motor function and delayed disease onset. Furthermore, KCHO-1 administration reduced oxidative stress through gp91 <superscript>phox</superscript> and the MAPK pathway in both classically activated microglia and the spinal cord of hSOD1 <superscript>G93A</superscript> transgenic mice. The results suggest that KCHO-1 can function as an effective therapeutic agent for ALS by reducing oxidative stress.
- Subjects :
- Amyotrophic Lateral Sclerosis physiopathology
Animals
Disease Models, Animal
Female
Mice
Mice, Transgenic
Amyotrophic Lateral Sclerosis drug therapy
Anti-Inflammatory Agents pharmacology
Motor Neurons drug effects
Oxidative Stress drug effects
Plant Extracts pharmacology
Plant Preparations pharmacology
Spinal Cord drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1976-555X
- Volume :
- 18
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Journal of veterinary science
- Publication Type :
- Academic Journal
- Accession number :
- 28385005
- Full Text :
- https://doi.org/10.4142/jvs.2017.18.4.487