DJ-1 based peptide, ND-13, promote functional recovery in mouse model of focal ischemic injury.
Lior MolchoTali Ben-ZurYael BarhumDaniel OffenPublished in: PloS one (2018)
Stroke is a leading cause of death worldwide and inflicts serious long-term damage and disability. The vasoconstrictor Endothelin-1, presenting long-term neurological deficits associated with excitotoxicity and oxidative stress is being increasingly used to induce focal ischemic injury as a model of stroke. A DJ-1 based peptide named ND-13 was shown to protect against glutamate toxicity, neurotoxic insults and oxidative stress in various animal models. Here we focus on the benefits of treatment with ND-13 on the functional outcome of focal ischemic injury. Wild type C57BL/6 mice treated with ND-13, after ischemic induction in this model, showed significant improvement in motor function, including improved body balance and motor coordination, and decreased motor asymmetry. We found that DJ-1 knockout mice are more sensitive to Endothelin-1 ischemic insult than wild type mice, contributing thereby additional evidence to the widely reported relevance of DJ-1 in neuroprotection. Furthermore, treatment of DJ-1 knockout mice with ND-13, following Endothelin-1 induced ischemia, resulted in significant improvement in motor functions, suggesting that ND-13 provides compensation for DJ-1 deficits. These preliminary results demonstrate a possible basis for clinical application of the ND-13 peptide to enhance neuroprotection in stroke patients.
Keyphrases
- wild type
- cerebral ischemia
- oxidative stress
- ischemia reperfusion injury
- subarachnoid hemorrhage
- diabetic rats
- mouse model
- brain injury
- traumatic brain injury
- blood brain barrier
- dna damage
- multiple sclerosis
- metabolic syndrome
- adipose tissue
- combination therapy
- heat shock
- newly diagnosed
- insulin resistance
- replacement therapy