Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5552996 | Biomedicine & Pharmacotherapy | 2017 | 8 Pages |
â¢SENP3 is significantly upregulated by chronic cerebral hypoperfusion.â¢URB597 could ameliorate neurovascular unit impairment and inhibit the expression of SENP3.â¢URB597 may be the potential neuroprotective treatment for neurovascular unit impairment induced by chronic cerebral hypoperfusion.
Disruption of the neurovascular unit (NVU), induced by chronic cerebral hypoperfusion (CCH), has been broadly found in various neurological disorders. SUMO-specific protease 3 (SENP3) is expressed in neurons, astrocytes, and microglia, and regulates a variety of cell events. However, whether SENP3 is involved in neurovascular injury under the condition of CCH is still elusive. To address this issue, we investigated the effect of the fatty acid amide hydrolase (FAAH) inhibitor URB597 on NVU and the role of SENP3 in this process, as well as the underling mechanisms. The expression of SENP3 was detected by immunochemistry. The function and structure of the NVU was assessed by Western blot analysis and transmission electron microscopy. CCH caused the upregulation of SENP3, the disruption of cell and non-cell components at the protein level within the NVU, and ultrastructural deterioration. The NVU impairment as well as overexpression of SENP3 were reversed by treatment with URB597. These results reveal a novel neuroprotective role in URB597, which implicates URB597 in the amelioration of CCH-induced NVU impairment by inhibiting SENP3.