Abstract
Background: Cerebral infraction seriously affects the life quality of patients. Danshensu has been reported to exhibit anti-inflammatory and vascular protective effects. However, the therapeutic function of Danshensu in cerebral vascular injury is still unclear.
Methods: Middle cerebral artery occlusion (MCAO) was used to construct the cerebral infraction model. Wound healing and tube formation assays were used to evaluate angiogenesis in vitro. Western blot assay was used to evaluate the activation of the PI3K/Akt/mTOR signaling pathway. The laser Doppler scanner was used to measure the regional cerebral blood flow (rCBF) in the area around the infarction, and the adhesion removal test was used to measure the sensorimotor function. The Modified Neurological Severity Score was performed to evaluate the cognitive functions of mice.
Results: Danshensu promoted the proliferation of bEnd.3 cells and angiogenesis in vitro. Danshensu upregulated the expression of VEGF through PI3K/Akt/mTOR signaling pathway in bEnd.3 cells. Danshensu improved rCBF restoration and attenuated the behavioral deficits in mice post-MCAO/R.
Conclusion: Danshensu enhances angiogenesis through the PI3K/Akt/mTOR/VEGF signaling pathway in a mouse model of cerebral ischemic injury.
Keywords: Cerebral infraction, VEGF, Danshensu, angiogenesis, MCAO, thrombiolytic therapy.
[http://dx.doi.org/10.1212/CON.0000000000000416] [PMID: 28157742]
[PMID: 30693691]
[http://dx.doi.org/10.5551/jat.43240] [PMID: 29877196]
[http://dx.doi.org/10.1159/000507190] [PMID: 32544913]
[http://dx.doi.org/10.1016/j.jns.2020.117182] [PMID: 33099172]
[http://dx.doi.org/10.1093/eurheartj/ehu218] [PMID: 24917641]
[http://dx.doi.org/10.1177/0897190018767769] [PMID: 29673293]
[http://dx.doi.org/10.1345/aph.18219] [PMID: 10332542]
[http://dx.doi.org/10.1016/S1051-0443(96)70810-2] [PMID: 8855542]
[http://dx.doi.org/10.2174/157016106776359880] [PMID: 16611153]
[http://dx.doi.org/10.1016/j.advms.2021.11.002] [PMID: 34781174]
[http://dx.doi.org/10.1016/j.cellimm.2021.104451] [PMID: 34781155]
[http://dx.doi.org/10.1016/j.prp.2021.153656] [PMID: 34749210]
[http://dx.doi.org/10.1002/ptr.7318] [PMID: 34709695]
[http://dx.doi.org/10.1016/j.jep.2021.114705] [PMID: 34655669]
[http://dx.doi.org/10.3791/2761] [PMID: 21372780]
[http://dx.doi.org/10.1371/journal.pone.0033444] [PMID: 22432023]
[http://dx.doi.org/10.1016/j.lfs.2021.119234] [PMID: 33607158]
[http://dx.doi.org/10.1177/1747493016647736] [PMID: 27145795]
[http://dx.doi.org/10.1016/S0140-6736(13)61088-0] [PMID: 24007975]
[http://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2018.09.053] [PMID: 30528672]
[http://dx.doi.org/10.1159/000494502] [PMID: 30408800]
[http://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2018.09.008] [PMID: 30309729]
[http://dx.doi.org/10.1186/s12929-019-0595-9] [PMID: 31900142]
[http://dx.doi.org/10.1016/j.pharmthera.2017.09.003] [PMID: 28942242]
[http://dx.doi.org/10.1016/j.redox.2013.04.001] [PMID: 24024167]
[http://dx.doi.org/10.1186/s12906-019-2738-7] [PMID: 32020857]
[http://dx.doi.org/10.1016/j.ejphar.2019.172710] [PMID: 31586468]
[http://dx.doi.org/10.1007/s11655-019-3165-9] [PMID: 31254156]
[http://dx.doi.org/10.1097/FBP.0000000000000412] [PMID: 29847337]
[http://dx.doi.org/10.1016/j.neuint.2019.104537] [PMID: 31425745]
[http://dx.doi.org/10.3389/fendo.2020.568436] [PMID: 33101201]
[http://dx.doi.org/10.1177/0300060520914218] [PMID: 32419546]