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Basics on the use of acid-sensing ion channels' inhibitors as therapeutics
被引:12
|作者:
Dibas, Jamileh
[1
]
Al-Saad, Houssam
[2
]
Dibas, Adnan
[2
]
机构:
[1] Appl Univ, Fac Pharm, Amman, Jordan
[2] Univ North Texas, Hlth Sci Ctr Ft Worth, Dept Pharmacol & Neurosci, North Texas Eye Res Inst, Ft Worth, TX 76107 USA
关键词:
optic nerve;
glaucoma;
neurodegeneration;
neuroprotection;
acid;
sensing;
ion channel;
calpain;
SEX-DIFFERENCES;
MODEL;
NEUROPROTECTION;
PAIN;
ACTIVATION;
AMILORIDE;
ISCHEMIA;
PEPTIDE;
TARGET;
HEAT-SHOCK-PROTEIN-70;
D O I:
10.4103/1673-5374.245466
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Since the discovery of acid-sensing ion channels in 1997, their importance in the health of neurons and other non-neuronal cells has gained significant importance. Acid-sensing ion channels play important roles in mediating pain sensation during diseases such as stroke, inflammation, arthritis, cancer, and recently migraine. More interestingly, acid-sensing ion channels may explain the sex differences in pain between males and females. Also, the ability of acid-sensing ion channel blockers to exert neuroprotective effects in a number of neurodegenerative diseases has added a new dimension to their therapeutic value. The current failure rate of similar to 45% of new drugs (due to toxicity issues) and saving of up to 7 years in the life span of drug approval makes drug repurposing a high priority. If acid-sensing ion channels' blockers undergo what is known as "drug repurposing", there is a great potential to bring them as medications with known safety profiles to new patient populations. However, the route of administration remains a big challenge due to their poor penetration of the blood brain and retinal barriers. In this review, the promise of using acid-sensing ion channel blockers as neuroprotective drugs is discussed.
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页码:395 / 398
页数:4
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