Stroke is said to beryllium nan 2nd starring origin of decease worldwide aft bosom disease. To forestall nan decease of neurons successful nan brain, a investigation group led by Osaka Metropolitan University Associate Professor Hidemitsu Nakajima of nan Graduate School of Veterinary Science has developed a supplier that inhibits a macromolecule progressive successful compartment death.
The multifunctional macromolecule GAPDH (glyceraldehyde-3-phosphate dehydrogenase) is linked to pathogenesis successful galore intractable encephalon and nervous system diseases. The squad developed GAI-17, a GAPDH aggregation inhibitor. When this inhibitor was administered to exemplary mice pinch acute strokes, location was a importantly little level of encephalon compartment decease and paralysis compared to untreated mice.
GAI-17 besides showed nary broadside effects of concern, specified arsenic adverse effects connected nan bosom aliases cerebrovascular system. Furthermore, experiments utilizing GAI-17 showed betterment successful nan mice moreover erstwhile administered six hours aft a stroke.
The GAPDH aggregation inhibitor we person developed is expected to beryllium a azygous supplier that tin dainty galore intractable neurological diseases, including Alzheimer's disease."
Hidemitsu Nakajima, Associate Professor, Osaka Metropolitan University
"Going forward, we will verify nan effectiveness of this attack successful illness models different than changeable and beforehand further applicable investigation toward nan realization of a patient and long-lived society."
The findings were published successful iScience.
Source:
Journal reference:
Kubo, T., et al. (2025) Inhibition of GAPDH aggregation arsenic a imaginable curen for acute ischemic stroke. iScience. doi.org/10.1016/j.isci.2025.112564.