系统性硬化症实验诱导中维生素d和α -生育酚醋酸酯对肺微循环的复杂作用

B. Doskaliuk, L. Zaiats
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The CG of rats received an isotonic solution following the same scheme, while the IG was not subjected to any injections. In addition to NaClO, the EG2 received intramuscular injections of vit E (10 mg/100 g) and vit D (1000 IU/100 g) for three weeks during the second half of the experiment. \nAfter 8 weeks, the animals were euthanized, and lung tissue samples were obtained for histological and electron microscopic analysis. The histological preparations were examined using light microscopy and photographed using a Leica DME light microscope, a DCM 900 digital microscope camera, and a Nicon Coolpix P5100 camera. Meanwhile, the electron microscopy was performed to visualize the ultrastructural characteristics of the lung tissue by use of \"PEM-125K\" (Selmi, Ukraine) with subsequent photography at magnifications from 2000 to 20000 times. \nAll animal procedures were carried out in strict compliance with bioethical principles. 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引用次数: 0

摘要

摘要本研究的目的是研究维生素D3(维生素D)和α -生育酚醋酸酯(维生素E)对系统性硬化症(SSc)实验模型肺微循环血管的影响。方法。我们将实验动物分为4组:完整组(IG) 15只,对照组(CG) 20只,实验1组(EG1)和实验2组(EG2)各25只。使用权方差最小化方法仔细进行分组随机化。为了诱导EG1实验动物SSc,采用5%次氯酸钠(NaClO) 0.5 ml皮下注射,每周3次,连续6周。大鼠CG按相同方案给予等渗溶液,IG不进行任何注射。在实验后半段,除NaClO外,EG2连续3周肌肉注射维生素E (10 mg/100 g)和维生素D (1000 IU/100 g)。8周后对大鼠实施安乐死,取肺组织标本进行组织学和电镜分析。光镜下观察组织学准备,采用徕卡DME光镜、DCM 900数码显微镜相机、尼康Coolpix P5100相机拍摄。同时,使用“PEM-125K”(Selmi,乌克兰)进行电镜观察肺组织的超微结构特征,随后在2000至20000倍的放大倍数下拍照。所有动物实验都严格遵守生物伦理原则。IFNMU伦理委员会于2020年11月19日批准了该研究,文件号为117/20。结果。CG动物肺标本组织学分析显示形态结构正常。在EG1中,肺部毛细血管结构异常,包括血管壁增厚引起的血管管腔狭窄、水肿和多形核细胞浸润。然而,在EG2中,组织学特征有所改善,水肿过程减少,多形核细胞浸润强度降低。EG1动物肺标本电镜检查显示血小板粘附和聚集,毛细血管腔内红细胞聚集。内皮细胞肿胀,毛细血管管腔变窄,基底膜不均匀增厚。相反,在EG2动物中,维生素D和E的组合可改善血液流变学特性和血液微循环元素的超微结构特征。毛细血管管腔内含有单个红细胞和失活血小板。内皮细胞膜的改变很小,轮廓清晰,无微胞泡或细胞质增生。内皮细胞细胞核呈细粒基质,染色质颗粒均匀分布。结论。本研究证明维生素D和E联合使用对实验性系统性硬化症肺微循环血管状态有积极影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE COMPLEX EFFECT OF VITAMIN D AND ALPHA TOCOPHEROL ACETATE ON THE LUNG MICROCIRCULATION IN THE EXPERIMENTAL INDUCTION OF SYSTEMIC SCLEROSIS
Abstract. The aim of the study was to investigate the effects of vitamin D3 (vitamin D) and alpha-tocopherol acetate (vitamin E) on the microcirculatory vessels of the lungs in an experimental model of systemic sclerosis (SSc). Methods. We divided the experimental animals into four separate groups: an intact group (IG) consisting of 15 animals, a control group (CG) of 20 animals, experimental group 1 (EG1) and experimental group 2 (EG2) consisting of of 25 animals each. Randomization of groups was carefully performed using the weight variance minimization method. To induce SSc in laboratory animals of EG1, subcutaneous injections of 0.5 ml of 5% sodium hypochlorite (NaClO) were administered 3 times a week for 6 weeks in a row. The CG of rats received an isotonic solution following the same scheme, while the IG was not subjected to any injections. In addition to NaClO, the EG2 received intramuscular injections of vit E (10 mg/100 g) and vit D (1000 IU/100 g) for three weeks during the second half of the experiment. After 8 weeks, the animals were euthanized, and lung tissue samples were obtained for histological and electron microscopic analysis. The histological preparations were examined using light microscopy and photographed using a Leica DME light microscope, a DCM 900 digital microscope camera, and a Nicon Coolpix P5100 camera. Meanwhile, the electron microscopy was performed to visualize the ultrastructural characteristics of the lung tissue by use of "PEM-125K" (Selmi, Ukraine) with subsequent photography at magnifications from 2000 to 20000 times. All animal procedures were carried out in strict compliance with bioethical principles. The Ethics Commission of the IFNMU granted approval for the study under document number 117/20 on November 19, 2020. Results. The histological analysis of the lung specimens of CG animals showed a normal morphological structure. In the EG1, the lungs exhibited abnormalities in the structure of the hemocapillaries, including narrowing of the vessel lumen due to thickening of the vascular wall, edema, and infiltration of polymorphonuclear cells. However, in the EG2, there was an improvement in the histological features, with a reduction in edematous processes and a decrease in the intensity of polymorphonuclear cell infiltration. The electron microscopic examination of the lung samples from EG1 animals revealed the presence of platelet adhesion and aggregation, as well as aggregates of erythrocytes within the hemocapillary lumen. Swelling of endothelial cells and narrowing of the hemocapillary lumen were also observed, along with uneven thickening of the basement membrane. In contrast, the combination of vitamins D and E in EG2 animals resulted in improved rheological properties of blood and ultrastructural characteristics of the hemomicrocirculatory elements. The lumen of the hemocapillaries contained single erythrocytes and inactive platelets. The endothelial cells’ membraines showed minimal alterations, with clear contours and no micropinocytotic vesicles or cytoplasmic growths. The nuclei of the endothelial cells had a fine-grained matrix with evenly distributed chromatin granules. Conclusions. This study proves that the combined use of vitamins D and E has a positive effect on the state of the microcirculatory vessels in the lungs of experimentally induced systemic sclerosis.
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