Ultrastructural changes in type 2 alveolocytes in young rats on the background of chronic hyperglycemia

Toufik Abdul-Rahman , Andrew Awuah Wireko , T.P. Teslyk , Serhii Dmytruk , Iryna Shkolna
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Abstract

Introduction

Diabetes mellitus (DM) is considered as a group of metabolic diseases with a global distribution and severe complications. It is caused by insulin deficiency, which with time leads to development of pathological changes in the cardiovascular, respiratory, and other systems. Several studies have shown some features and the connection of structural changes of the lungs with DM, however very little is known regarding ultrastructural changes of type 2 alveolocytes (AT2).

Materials and methods

The study involved 24 white non-linear male laboratory rats which were divided into two groups (experimental and intact). The experimental group was further divided into two subgroups depending on the duration of study: the first group with hyperglycemia for 30 days, and the second with hyperglycemia for 60 days. For the experimental modeling of hyperglycemia, the rats were injected once subcutaneously with solution of alloxan monohydrate hyperglycemia.

Results

AT2 of the intact group had a high degree of differentiation with plates of high electron density. In AT2 of rats with hyperglycemia for 30 days, there were signs of vacuolation, mass accumulation of primary and secondary lysosomes, and lamellar bodies were grouped as conglomerates. In AT2 of the rats with 60 days of hyperglycemia, nuclei with scalloped contour, karyoplasmic outgrowths and intussusception, and condensation of heterochromatin were observed.

Conclusion

Under conditions of experimental chronic hyperglycemia, proliferation and destruction of AT2 are observed, which is the morphological basis for the violation of surfactant synthesis and immunocompetent properties in lung tissues of young rats.

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慢性高血糖背景下幼龄大鼠2型肺泡细胞超微结构变化
糖尿病(DM)被认为是一组全球性分布和严重并发症的代谢性疾病。它是由胰岛素缺乏引起的,随着时间的推移,导致心血管、呼吸和其他系统的病理改变。一些研究显示了一些特征和肺结构变化与DM的联系,但对2型肺泡细胞(AT2)的超微结构变化知之甚少。材料与方法实验用雄性非线性白色实验大鼠24只,分为实验组和完整组。根据研究持续时间将实验组进一步分为两个亚组:第一组高血糖30天,第二组高血糖60天。为建立高血糖模型,大鼠皮下注射四氧嘧啶一水高血糖液一次。结果完整组sat2分化程度高,电子密度高;高血糖30 d大鼠AT2出现空泡现象,原发性和继发性溶酶体大量堆积,片层体呈聚集体。高血糖60 d大鼠AT2观察到核呈扇形,核质增生,肠套叠,异染色质凝集。结论在实验性慢性高血糖条件下,观察到AT2的增殖和破坏,这是幼年大鼠肺组织中表面活性物质合成和免疫活性受到破坏的形态学基础。
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来源期刊
Endocrine and Metabolic Science
Endocrine and Metabolic Science Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.80
自引率
0.00%
发文量
4
审稿时长
84 days
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