Use of Crassifolin A in preparation of drug for promoting mitophagy and treating neurodegenerative diseases
Disclosed in the present invention is the use of Crassifolin A in promoting mitophagy and treating neurodegenerative diseases. According to the present invention, experiments show that the diterpene compound Crassifolin A can significantly increase mitophagy levels, promote the removal of damaged mitochondria, maintain homeostasis in cells, and has potential effects of treating neurodegenerative diseases and other related diseases; moreover, Crassifolin A is a small-molecule compound that can easily penetrate through the blood-brain barrier to reach the brain so as to play a role, can be extracted from a Thickleaf croton root medicinal material, has the advantages of abundant medicinal sources, easy availability, low drug toxicity and few side effects, and has a good application prospect in the treatment of neurodegenerative diseases.
1 . A method for promoting cellular mitophagy in vitro, comprising providing an effective amount of Crassifolin A to cultured human cells, wherein the Crassifolin A has the following chemical structural formula as shown in Formula (I):
2 . The method according to claim 1 , wherein the effective concentration of the provided Crassifolin A is 5-15 μmol/L.
3 . The method according to claim 2 , wherein the effective concentration of the provided Crassifolin A is 10 μmol/L.
4 . A method for treatment of a neurodegenerative disease, comprising administering to a subject an effective amount of Crassifolin A, wherein the Crassifolin A has the following chemical structural formula as shown in Formula (I):
thereby treating the neurodegenerative disease.
5 . The method according to claim 4 , wherein the the Crassifolin A promotes mitophagy and inhibits expression of phosphorylated Tau, thereby treating the neurodegenerative disease.
6 . The method according to claim 4 , wherein the neurodegenerative disease is selected from the group consisting of Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, a spinal cerebellar ataxia, Pick's disease, cerebral ischemia, brain injury, and epilepsy.