The Vasorelaxant and Neuroprotective Effects of Mildronate in A Rabbit Subarachnoid Hemorrhage Model

被引:3
作者
Eser, Muhammed Taha [1 ]
Bektasoglu, Pinar Kuru [2 ,3 ]
Gurer, Bora [2 ]
Bozkurt, Huseyin [4 ]
Sorar, Mehmet [1 ]
Ozturk, Ozden Caglar [2 ]
Arikok, Ata Turker [5 ]
Kertmen, Hayri [1 ]
机构
[1] Univ Hlth Sci, Diskapi Educ & Res Hosp, Dept Neurosurg, Turkish Minist Hlth, Ankara, Turkey
[2] Univ Hlth Sci, Fatih Sultan Mehmet Educ & Res Hosp, Dept Neurosurg, Turkish Minist Hlth, Istanbul, Turkey
[3] Marmara Univ, Dept Physiol, Sch Med, Istanbul, Turkey
[4] Cumhuriyet Univ, Dept Neurosurg, Sch Med, Sivas, Turkey
[5] Univ Hlth Sci, Diskapi Educ & Res Hosp, Dept Pathol, Turkish Minist Hlth, Ankara, Turkey
关键词
Anti-ischemic; Mildronate; Neuroprotection; Rabbit; Subarachnoid hemorrhage; GAMMA-BUTYROBETAINE; CEREBRAL VASOSPASM; DOUBLE-BLIND; ORAL NIMODIPINE; INHIBITOR; ERYTHROPOIETIN; THERAPY; ARTERY;
D O I
10.5137/1019-5149.JTN.24647-18.3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
AIM: To investigate the effects of an anti-ischemic agent, mildronate, on subarachnoid hemorrhage-induced vasospasm. MATERIAL and METHODS: Rabbits were randomly divided into four groups: control, subarachnoid hemorrhage (SAH), vehicle, and mildronate (n=8 animals per group). In the treatment group, 200 mg/kg of mildronate were intraperitoneally administered 5 minutes after the procedure and continued for 3 days as daily administrations of the same dose. At the end of the third day, the cerebrum, cerebellum, and brain stem were perfused, fixated, and removed for histopathological examination. Tissues were examined for arterial wall thickness, luminal area, and hippocampal neuronal degeneration. RESULTS: Mildronate group showed significantly increased luminal area and reduced wall thickness of the basilar artery compared with the subarachnoid hemorrhage group. In addition, the hippocampal cell degeneration score was significantly lower in the mildronate group than in the SAH and vehicle groups. CONCLUSION: These results show that mildronate exerts protective effects against SAH-induced vasospasm and secondary neural injury.
引用
收藏
页码:163 / 170
页数:8
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