TABLE 1.
Comparison of the neuroprotective effects of FTY720 in different methods of ischemic stroke in experimental and clinical studies
Author, year | Stroke models | Different animal species | Different doses of FTY720 | Method of administration | Results | Reference |
---|---|---|---|---|---|---|
Brait VH, 2016 | 45 min MCAO and reperfusion | Mice | 1 mg/kg | Intraperitoneal (i.p.) | FTY720 reduced infarct volume | Brait et al. (2016) |
Salas‐Perdomo, 2019 | 45 min MCAO and reperfusion | Mice | 1 mg/kg | i.p. | Fingolimod attenuated the extent of bleeding and improved the neurological score | Salas‐Perdomo et al. (2019) |
Nazari M, 2016 | 60 min MCAO and reperfusion | Male Sprague‐Dawley rats | 0.5 mg/kg | i.p. | FTY720 improved the infarct volume and memory performance | Nazari et al. (2016) |
Czech B, 2009 |
90 min MCAO and reperfusion | C57Bl/6 mice | 1 mg/kg | i.p. | FTY720 reduced lesion size and improved neurological function | Czech et al. (2009) |
Wacker BK, 2009 | 60 min tMCAO and 24 hr of reperfusion | Adult male Swiss‐Webster ND4 mice | 0.24 or 1 mg/kg | i.p | FTY720 dose‐dependently decreased infarct size and neurological deficit | Wacker et al. (2009) |
Wei Y, 2011 | 90 min tMCAO and reperfusion/ Permanent MCAO | Rat/ C57BL/6 male mice | 0.5 or 1 mg/kg | i.p. | FTY720 reduced infarct size and neurological deficit | Wei et al. (2011) |
Hasegawa Y, 2013 | 120 min tMCAO and reperfusion | Sprague‐Dawley rats | 0.25 mg/kg | i.p. | FTY720 improved infarction size and neurological function | Hasegawa et al. (2013) |
Hasegawa Y, 2010 | 120 min tMCAO and reperfusion | Sprague‐Dawley rats | 0.25, 1 mg/kg | i.p. | FTY720 significantly reduced infarct volume and improved neurological score | Hasegawa et al. (2010) |
Kraft P, 2013 | 60 or 90 min tMCAO and reperfusion | C57Bl/6 mice | 1 mg/kg | i.p. | FTY720 significantly reduced stroke size and improved functional outcome | Kraft et al. (2013) |
Moon E, 2015 | 60 or 90 min tMCAO and reperfusion | ICR male mice | 3 mg/kg | i.p. | FTY720 reduced ischemic brain damage | Moon et al. (2015) |
Pfeilschifter,W, 2011 | 120 min tMCAO and reperfusion | C57Bl/6 mice | 1 mg/kg | i.p. | FTY720 was effective in improvement of brain injury | Pfeilschifter et al. (2011) |
Shichita, 2009 | 60 min MCAO and reperfusion | C57/BL/6 male mice | 1 mg/kg | Intravenous (i.v.) | FTY720 reduced I/R‐induced brain damage reduced infarct volume | Shichita et al. (2009) |
Liesz A, 2011 | 60 min Permanent MCAO | C57BL/6 male mice | 1 mg/kg | i.p. | FTY720 did not reduce infarct volumes and improve behavioral dysfunction | Liesz et al. (2011) |
Qin Ch, 2017 | Hypoperfusion‐induced White matter ischemic injury | C57Bl/6 mice | 0.3 mg/kg | i.p. | FTY720 has neuroprotective effect in acute ischemic stroke | Qin et al. (2017) |
Campos F, 2013 | 80 min thromboembolic occlusion and reperfusion | C57BL/6 male mice | 0.5 mg/kg | i.p. | Fingolimod attenuated the neurological deficit and infarct volume | Campos et al. (2013) |
Brunkhorst R,2013 | 15 min photothrombosis | C57BL/6 male mice | 1 mg/kg | i.p. | FTY720 has a positive impact on long‐term functional outcome | Brunkhorst et al. (2013) |
Li X,2017 | 20 min thromboembolic occlusion | C57/BL/6 male mice | 0.5, 1, or 2 mg/kg | i.p. | FTY720, attenuated cerebral infarction, neuronal apoptosis, and improved neurological deficits | Li et al. (2017) |
Shang K, 2020 | 15 min thromboembolic occlusion | C57/BL/6 male mice | 0.3 mg/kg | i.p. | FTY720 reduced neuronal loss and improved motor function | Shang et al. (2020) |
Yang D, 2014 | 90 min hypoxic–ischemic (HI) | Wistar rat pups | 0.3 or 1 μg/g, | i.p. | FTY720 prevent inflammation‐sensitized hypoxic–ischemic brain injury in newborns | Yang et al. (2014) |
Fu Y, 2014 | Patients with acute ischemic stroke | 0.5 mg/day | Orally for 3 consecutive days | FTY720 decreased lesion size, microvascular permeability and attenuated neurological deficits | Fu et al. (2014) | |
Zhu Z, 2015 | Patients with acute ischemic stroke | 0.5 mg/day | Orally for 3 consecutive days | FTY720 plus alteplase reduced infarction size, hemorrhage volume and improved clinical outcomes | Zhu et al., (2015) |