Riger N A, Trushina E N, Mustafina O K, Timonin A N, Aksenov I V, Guseva G V, Tutelyan V A
Federal Research Centre of Nutrition, Biotechnology and Food Safety, 109240, Moscow, Russian Federation.
I.M. Sechenov First Moscow State Medical of Ministry of Healthcare of the Russian Federation University (Sechenov University), 119991, Moscow, Russian Federation.
Vopr Pitan. 2021;90(3):6-19. doi: 10.33029/0042-8833-2021-90-3-6-19. Epub 2021 May 17.
The study of the relationship between hematopoiesis and metabolism is now particularly relevant in view of the high incidence of alimentary dependent diseases, including non-alcoholic fatty liver disease. In this regard, pathogenetic factors of this disease development are studied actively in order to choose adequate drug therapy and usage of bioactive substances with antioxidant properties. of the study was to study the pathogenetic relationship of hematological disorders and imbalance of growth factors, leptin and ghrelin in male Wistar rats in the model of the initial stage of non-alcoholic fatty liver disease development and to assess the regulatory effect of minor bioactive substances - carnosine and α-lipoic acid. . The studies were performed on male Wistar rats with initial body weight 150±10 g within 8 weeks. Animals were divided into 5 groups (n=8 in each). Rats of the control group received a complete modified diet AIN93M, in which soybean oil was replaced with sunflower oil and lard (1:1). Rats of the experimental groups consumed high-calorie choline-deficient diet (HCCDD), in which fat content was 45%, fructose content - 20% of the energy value of the diet. Rats of the 2nd group were fed HCCDD without any supplements, the 3rd group - with the addition of carnosine (75 mg/kg body weight), the 4th group - with the addition of α-lipoic acid (75 mg/kg body weight), the 5th group - with the combined addition of carnosine and α-lipoic acid in a total dose of 150 mg/kg body weight. Hematological values were determined on a hematological analyzer. The content of ghrelin and leptin, as well as growth factors GM-CSF and M-CSF in blood plasma and adipose tissue lysates, was determined by multiplex immunoassay using xMAP technology. . Rat intake of HCCDD resulted in decreased hemoglobin levels and red blood cell scores compared to controls. Diet enrichment with carnosine and α-lipoic acid did not have a reliable effect on these indicators. Carnosine intake had a protective effect on erythrocyte volume, a decrease of which was recorded in other experimental groups. HCCDD stimulated the growth of the absolute number of leukocytes in peripheral blood due to granulocytes and mononuclears. The enrichment of HCCDD with carnosine and α-lipoic acid led to a further increase in leukocytosis, the maximum level of which was observed in the group of rats fed HCCDD, simultaneously enriched with carnosine and α-lipoic acid (14.86±1.48×10/l compared to 8.67±1.23×10/l in control). All diets used in the research had no effect on the number of erythrocytes and platelets in the peripheral blood of rats. The use of both HCCDD alone and in combination with carnosine or α-lipoic acid intake had a negative effect on the level of growth factors GM-CSF and M-CSF in blood plasma and adipose tissue. The consumption of HCCDD caused an increase in leptin blood level (8.54±0.69 compared to 2.58±0.37 pg/ml in control, р<0.05), which was normalized by enriching the diet with carnosine and α-lipoic acid. Ghrelin blood level significantly decreased in all experimental groups compared to the control: by 30% in rats fed and by almost 50% when carnosine and α-lipoic acid were added to HCCDD. The intake of α-lipoic acid led to hormone level changes in adipose tissue lysates, leptin content decreased (2.31±0.11 vs 2.77±0.15 pg/ml), while ghrelin level significantly increased (0.35±0.14 vs 0.20±0.06 pg/ml), compared with the control group (р<0.05). . The revealed interrelation of parameters of the cellular composition of peripheral blood and hemoglobin content with the changes in the content of GM-CSF, M-CSF, leptin and ghrelin in blood plasma and adipose tissue indicates the mutual influence of the studied CSF, leptin, ghrelin and added antioxidants (carnosine and α-lipoic acid) on the regulatory mechanisms of hematopoiesis in rats fed HCCDD.
鉴于包括非酒精性脂肪肝病在内的营养依赖性疾病的高发病率,造血与代谢之间关系的研究目前尤为重要。在这方面,人们积极研究该疾病发展的致病因素,以便选择适当的药物治疗方法并使用具有抗氧化特性的生物活性物质。本研究的目的是在非酒精性脂肪肝病发展初期的模型中,研究雄性Wistar大鼠血液系统紊乱与生长因子、瘦素和胃饥饿素失衡之间的致病关系,并评估微量生物活性物质——肌肽和α-硫辛酸的调节作用。研究在初始体重为150±10 g的雄性Wistar大鼠身上进行,为期8周。动物被分为5组(每组n = 8)。对照组大鼠接受完全改良的AIN93M饮食,其中大豆油被向日葵油和猪油(1:1)替代。实验组大鼠食用高热量胆碱缺乏饮食(HCCDD),其中脂肪含量为45%,果糖含量为饮食能量值的20%。第2组大鼠喂食HCCDD且无任何补充剂,第3组——添加肌肽(75 mg/kg体重),第4组——添加α-硫辛酸(75 mg/kg体重),第5组——联合添加肌肽和α-硫辛酸,总剂量为150 mg/kg体重。血液学指标在血液分析仪上测定。血浆和脂肪组织裂解物中胃饥饿素和瘦素以及生长因子GM-CSF和M-CSF的含量,采用xMAP技术通过多重免疫测定法测定。与对照组相比,大鼠摄入HCCDD导致血红蛋白水平和红细胞计数降低。用肌肽和α-硫辛酸丰富饮食对这些指标没有可靠影响。摄入肌肽对红细胞体积有保护作用,其他实验组记录到红细胞体积减小。由于粒细胞和单核细胞,HCCDD刺激外周血白细胞绝对数量增加。用肌肽和α-硫辛酸丰富HCCDD导致白细胞增多进一步增加,在同时添加肌肽和α-硫辛酸的HCCDD喂养大鼠组中观察到最高水平(14.86±1.48×10⁹/l,而对照组为8.67±1.23×10⁹/l)。研究中使用的所有饮食对大鼠外周血红细胞和血小板数量均无影响。单独使用HCCDD以及与肌肽或α-硫辛酸联合摄入,均对血浆和脂肪组织中生长因子GM-CSF和M-CSF水平有负面影响。摄入HCCDD导致血浆瘦素水平升高(8.54±0.69,而对照组为2.58±0.37 pg/ml,p<0.0),用肌肽和α-硫辛酸丰富饮食可使其恢复正常。与对照组相比,所有实验组血浆胃饥饿素水平均显著降低:喂食大鼠降低30%,在HCCDD中添加肌肽和α-硫辛酸时降低近50%。摄入α-硫辛酸导致脂肪组织裂解物中激素水平变化,瘦素含量降低(2.31±0.11对2.77±0.15 pg/ml),而胃饥饿素水平显著升高(0.35±0.14对0.20±0.06 pg/ml),与对照组相比(p<0.05)。外周血细胞组成参数和血红蛋白含量与血浆和脂肪组织中GM-CSF、M-CSF、瘦素和胃饥饿素含量变化之间的相互关系表明,所研究的CSF、瘦素、胃饥饿素和添加的抗氧化剂(肌肽和α-硫辛酸)对喂食HCCDD大鼠的造血调节机制有相互影响。