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一项关于内括约肌在大便失禁方面的翻译及实验研究的系统评价。

A systematic review of translation and experimental studies on internal anal sphincter for fecal incontinence.

作者信息

Kim Minsung, Oh Bo-Young, Lee Ji-Seon, Yoon Dogeon, Chun Wook, Son Il Tae

机构信息

Department of Surgery, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang, Korea.

Burn Institute, Hangang Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea.

出版信息

Ann Coloproctol. 2022 Jun;38(3):183-196. doi: 10.3393/ac.2022.00276.0039. Epub 2022 Jun 9.

Abstract

The complexity in the molecular mechanism of the internal anal sphincter (IAS) limits preclinical or clinical outcomes of fecal incontinence (FI) treatment. So far, there are no systematic reviews of IAS translation and experimental studies that have been reported. This systematic review aims to provide a comprehensive understanding of IAS critical role in FI. Previous studies revealed the key pathway for basal tone and relaxation of IAS in different properties as follows; calcium, Rho-associated, coiled-coil containing serine/threonine kinase, aging-associated IAS dysfunction, oxidative stress, renin-angiotensin-aldosterone, cyclooxygenase, and inhibitory neurotransmitters. Previous studies have reported improved functional outcomes of cellular treatment for regeneration of dysfunctional IAS, using various stem cells, but did not demonstrate the interrelationship between those results and basal tone or relaxation-related molecular pathway of IAS. Furthermore, these results have lower specificity for IAS-incontinence due to the included external anal sphincter or nerve injury regardless of the cell type. An acellular approach using bioengineered IAS showed a physiologic response of basal tone and relaxation response similar to human IAS. However, in both cellular and acellular approaches, the lack of human IAS data still hampers clinical application. Therefore, the IAS regeneration presents more challenges and warrants more advances.

摘要

肛管内括约肌(IAS)分子机制的复杂性限制了大便失禁(FI)治疗的临床前或临床效果。到目前为止,尚未有关于IAS转化和实验研究的系统综述报道。本系统综述旨在全面了解IAS在FI中的关键作用。先前的研究揭示了IAS在不同特性下基础张力和松弛的关键途径如下:钙、Rho相关的含卷曲螺旋的丝氨酸/苏氨酸激酶、衰老相关的IAS功能障碍、氧化应激、肾素-血管紧张素-醛固酮、环氧化酶和抑制性神经递质。先前的研究报道了使用各种干细胞对功能失调的IAS进行再生的细胞治疗的功能改善结果,但未证明这些结果与IAS的基础张力或松弛相关分子途径之间的相互关系。此外,由于纳入了外括约肌或神经损伤,无论细胞类型如何,这些结果对IAS失禁的特异性较低。使用生物工程IAS的无细胞方法显示出与人类IAS相似的基础张力生理反应和松弛反应。然而,在细胞和无细胞方法中,缺乏人类IAS数据仍然阻碍了临床应用。因此,IAS再生面临更多挑战,需要更多进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df6/9263305/449a5a9cead1/ac-2022-00276-0039f1.jpg

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