Kendir-Demirkol Yasemin, Jenny Laura A, Demirkol Aykut, Özen Metahan, Ayata Ali, Canatan Duran
Department of Pediatrics, Süleyman Demirel University Faculty of Medicine, Isparta, Türkiye.
Department of Ophthalmology, Columbia University Medical Center, New York, United States.
Turk Arch Pediatr. 2023 May;58(3):298-301. doi: 10.5152/TurkArchPediatr.2023.21363.
Linezolid is often used to treat antibacterial-resistant infections. Linezolid can cause side effects. To date, the effectiveness of the simultaneous administration of pyridoxine and linezolid is unclear. Here we investigate the protective effect of pyridoxine on linezolid-induced hematological toxicity, hepatotoxicity, and oxidative stress in rats.
The 40 male pediatric Spraque-Dawley rats were separated into 4 groups: control, linezolid, pyridoxine, and linezolid-pyridoxine. A complete blood count, liver function test, and measurements of antioxidant enzyme activities for superoxide dismutase, glutathione peroxidase, catalase, and lipid peroxidation were performed in blood before treatment and 2 weeks after administration of the treatment.
White blood cell and hemoglobin counts for the linezolid group decreased, and the alanine aminotransferase level in the linezolid group increased compared to their respective baseline values. Post-treatment white blood cell decreased in the linezolid and linezolid- pyridoxine groups compared to those in the control group (P < .001). Alanine aminotransferase levels increased in the linezolid and linezolid-pyridoxine groups compared to those in the control group (P < .001 and P < .05, respectively). The activity of superoxide dismutase, catalase, glutathione peroxidase, and malondialdehyde levels increased in the linezolid group compared to the control group (P < .001, P < .05, P < .001, and P < .001, respectively). Linezolid plus pyridoxine treatment caused a significant decrease in malondialdehyde levels and superoxide dismutase, catalase, and glutathione peroxidase enzyme activities compared to the linezolid group (P < .001, P < .01, P < .001, and P < .01, respectively).
Pyridoxine may be an effective adjuvant agent for the prevention of linezolid toxicity in rat models.
利奈唑胺常用于治疗耐抗菌感染。利奈唑胺会引起副作用。迄今为止,同时给予吡哆醇和利奈唑胺的有效性尚不清楚。在此,我们研究吡哆醇对利奈唑胺诱导的大鼠血液毒性、肝毒性和氧化应激的保护作用。
将40只雄性幼年斯普拉格-道利大鼠分为4组:对照组、利奈唑胺组、吡哆醇组和利奈唑胺-吡哆醇组。在治疗前及给药2周后,对血液进行全血细胞计数、肝功能测试,并测量超氧化物歧化酶、谷胱甘肽过氧化物酶、过氧化氢酶的抗氧化酶活性及脂质过氧化水平。
与各自的基线值相比,利奈唑胺组的白细胞和血红蛋白计数降低,丙氨酸转氨酶水平升高。与对照组相比,治疗后利奈唑胺组和利奈唑胺-吡哆醇组的白细胞减少(P < 0.001)。与对照组相比,利奈唑胺组和利奈唑胺-吡哆醇组的丙氨酸转氨酶水平升高(分别为P < 0.001和P < 0.05)。与对照组相比,利奈唑胺组的超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶活性及丙二醛水平升高(分别为P < 0.001、P < 0.05、P < 0.001和P < 0.001)。与利奈唑胺组相比,利奈唑胺加吡哆醇治疗使丙二醛水平及超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶活性显著降低(分别为P < 0.001、P < 0.01、P < 0.001和P < 0.01)。
在大鼠模型中,吡哆醇可能是预防利奈唑胺毒性的有效辅助药物。