Creatine lysinate – part I: investigation of the toxicity and the influence on some biochemical parameters in mice

IF 1.1 Q4 PHARMACOLOGY & PHARMACY Pharmacia Pub Date : 2023-09-28 DOI:10.3897/pharmacia.70.e109446
Ivanka Kostadinova, Nikolai Danchev, Boycho Landzhov, Lyubomir Marinov, Ivalina Ivanova, Dobrina Tsvetkova
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Abstract

In our study we investigated the acute toxicity of а newly synthesized creatine lysinate as well as its effect on the biochemical parameters in mice. Creatine lysinate exerts better solubility in water (3.3%) in comparison to creatine monohydrate (1.4%) at 20 °C and it is determined as a non-toxic after intraperitoneal (LD50 – 4543 mg/kg) and oral administration (LD50 > 8000 mg/kg). Oral administration of creatine lysinate at doses of 3 g/kg/day and 6 g/kg/day for 2 weeks reduced the creatine kinase levels, which indicates muscle protection. An increased levels of liver enzymes like alanine aminotransferase (ALAT) and aspartate aminotransferase (ASAT) was observed after the supplementation with creatine lysinate at both administered doses and the level of lactate was comparable both in the studied and the control group.
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赖氨酸肌酸酯-第一部分:毒性及对小鼠某些生化指标影响的研究
本实验研究了新合成的溶肌酸酯对小鼠的急性毒性及其对小鼠生化指标的影响。在20°C时,与一水肌酸(1.4%)相比,赖氨酸肌酸在水中的溶解度(3.3%)更好,经腹腔注射(LD50 - 4543 mg/kg)和口服(LD50 >8000毫克/公斤)。口服溶肌酸3 g/kg/天和6 g/kg/天,持续2周,可降低肌酸激酶水平,表明肌肉有保护作用。在补充两种给药剂量的赖氨酸肌酸后,观察到肝酶如丙氨酸转氨酶(ALAT)和天冬氨酸转氨酶(ASAT)水平升高,乳酸水平在研究组和对照组中都是相当的。
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来源期刊
Pharmacia
Pharmacia PHARMACOLOGY & PHARMACY-
CiteScore
2.30
自引率
27.30%
发文量
114
审稿时长
12 weeks
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