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CCL4、BCL2A1 和 NFKBIA 基因与阴虚体质女性早老的关系。

The relationship of CCL4, BCL2A1, and NFKBIA genes with premature aging in women of Yin deficiency constitution.

机构信息

National Institute of Traditional Chinese Medicine Constitution and Preventive Medicine, Beijing University of Chinese Medicine, Beijing 100029, China.

School of Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China.

出版信息

Exp Gerontol. 2021 Jul 1;149:111316. doi: 10.1016/j.exger.2021.111316. Epub 2021 Mar 23.

Abstract

BACKGROUND

Traditional Chinese Medicine (TCM) defined constitution as a health statue or physical fitness that determines individual susceptibility to diseases. Yin deficiency constitution (YinDC) is a type of constitution closely related to aging. Previous studies found that the characteristic genes of YinDC are part of the inflammatory aging signaling pathways (e.g., NF-kappa B). Therefore, the aim of the study was to further reveal the dysregulation of genes associated with inflammatory aging in YinDC women.

METHODS

This study adopted the industrial standard of constitutional judgment, and screened YinDC (n = 30) and Balanced constitution (BC) (n = 30) from women between the ages of 35 to 49, a range categorized as the degenerating period by TCM. Five genes CCL4, BCL2A1, NFKBIA, TAK1, and IL-8 were analyzed by qRT-PCR.

RESULTS

Logistical regression revealed the correlation between body constitution and the expression of the five genes: the expression of NFKBIA and CCL4 mRNA was significantly up-regulated, whereas the expression of BCL2A1 mRNA was significantly down-regulated in YinDC (P < 0.05). Age or weight, when included in the model, did not affected the correlations.

CONCLUSION

Increased mRNA expression of CCL4 and NFKBIA and decreased mRNA expression of BCL2A1 may be the molecular basis of premature aging of YinDC women. These results provide a mechanistic basis for early conditioning of YinDC, anti-aging, and the prevention of aging-related diseases.

摘要

背景

中医(TCM)将体质定义为决定个体易患疾病的健康状态或身体状况。阴虚体质(YinDC)是一种与衰老密切相关的体质。先前的研究发现,YinDC 的特征基因是炎症衰老信号通路的一部分(例如 NF-kappa B)。因此,本研究旨在进一步揭示 YinDC 女性中与炎症性衰老相关的基因失调。

方法

本研究采用体质判断的工业标准,从年龄在 35 至 49 岁之间的女性中筛选出 YinDC(n=30)和平衡体质(BC)(n=30),这一年龄范围在中医中被归类为退化期。通过 qRT-PCR 分析了五个基因 CCL4、BCL2A1、NFKBIA、TAK1 和 IL-8。

结果

逻辑回归显示体质与五个基因表达之间的相关性:YinDC 中 NFKBIA 和 CCL4 mRNA 的表达明显上调,而 BCL2A1 mRNA 的表达明显下调(P<0.05)。在模型中包含年龄或体重时,并不影响相关性。

结论

CCL4 和 NFKBIA mRNA 的表达增加以及 BCL2A1 mRNA 的表达减少可能是 YinDC 女性早衰的分子基础。这些结果为 YinDC 的早期调理、抗衰老和预防与衰老相关的疾病提供了机制基础。

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