Neuroprotective Effects of Coenzyme Q10 and Ozone Therapy on Experimental Traumatic Spinal Cord Injuries in Rats

被引:2
|
作者
Gel, Gulce [1 ]
Unluer, Caner [1 ]
Yilmaz, Erdal Resit [1 ]
Erguder, Berrin Imge [2 ]
Arikok, Ata Turker [3 ]
Sener, Serkan [1 ]
Kertmen, Huseyin Hayri [1 ]
Turkoglu, Mehmet Erhan [1 ]
机构
[1] Univ Hlth Sci, Diskapi Educ & Res Hosp, Dept Neurosurg, Ankara, Turkiye
[2] Ankara Univ, Sch Med, Dept Biochem, Ankara, Turkiye
[3] Acibadem Univ Hosp, Dept Emergency, Ankara, Turkiye
关键词
Antioxidants; Oxidative stress; Ozone; Spinal cord injury; ISCHEMIA/ REPERFUSION INJURY; OXIDATIVE STRESS; CASPASE-3; ACTIVATION; CONTROLLED-TRIAL; CELL-DEATH; APOPTOSIS; METHYLPREDNISOLONE; MITOCHONDRIA; INFLAMMATION; PREVALENCE;
D O I
10.1016/j.wneu.2024.04.141
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
-OBJECTIVE: This study investigates the neuroprotective effects and functional recovery potential of Coenzyme Q10 (CoQ10) and ozone therapy in spinal cord injury (SCI). MATERIAL AND METHODS: In this study, 40 female Sprague-Dawley rats were divided into 5 groups of 8. Surgical procedures induced spinal cord trauma in all groups, except the control group. The ozone group received 0.7 mg/kg rectal ozone daily for 7 days, starting 1 hour postspinal cord trauma. The CoQ10 group was administered 120 mg/kg CoQ10 orally once daily for 7 days, beginning 24 hours prior to trauma. The CoQ10 + ozone group received both treatments. Examinations included a modified Tarlov scale and inclined plane test on days 1, 3, 5, and 7. Malondialdehyde (MDA) analysis was conducted on serum samples, and assessments of caspase-3, Bcl-2, and Bax levels were performed on tissue samples. Additionally, a comprehensive examination analyzed histopathological and ultrastructural changes. RESULTS: After SCI, there was a statistically significant increase in serum MDA, tissue caspase-3, and Bax levels (MDA P < 0.001, caspase-3 P < 0.001, Bax P = 0.003). In the CoQ10 + ozone group, serum MDA ( P = 0.002), tissue caspase-3 ( P = 0.001), and Bax ( P = 0.030) levels were significantly lower compared to the trauma group. Tissue Bcl-2 levels were also significantly higher ( P = 0.019). The combined treatment group demonstrated improved histopathological, ultrastructural, and neurological outcomes. CONCLUSIONS: This study shows that CoQ10 + ozone therapy in traumatic SCI demonstrates neuroprotective effects via antioxidant and antiapoptotic mechanisms. The positive effects on functional recovery are supported by data from biochemical, histopathological, ultrastructural, and neurological examinations.
引用
收藏
页码:E25 / E33
页数:9
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