Animal models closer to intrauterine adhesive pathology
Editorial

Animal models closer to intrauterine adhesive pathology

Sung Woo Kim, Yoon Young Kim, Hoon Kim, Seung-Yup Ku

Department of Obstetrics and Gynecology, Seoul National University Hospital, Seoul, South Korea

Correspondence to: Seung-Yup Ku, MD, PhD. Department of Obstetrics and Gynecology, Seoul National University Hospital, Seoul, South Korea. Email: jyhsyk@snu.ac.kr.

Comment on: Feng Q, Gao B, Zhao X, et al. Establishment of an animal model of intrauterine adhesions after surgical abortion and curettage in pregnant rats. Ann Transl Med 2020;8:56.


Submitted Apr 28, 2020. Accepted for publication Jun 05, 2020.

doi: 10.21037/atm-20-3598


Although the true incidence of intrauterine adhesion (IUA) is uncertain, the prevalence of IUA after curettage is reported to be between 15% and 40% (1). IUA may cause menstrual disorders as well as adverse reproductive outcomes such as subfertility, infertility and recurrent miscarriage. Among the aforementioned, IUA was found in 4.6% of infertile women, and 21.8% in those with recurrent pregnancy loss (2,3). Endometrial factor is much more difficult to treat than other infertility factors such as anovulation, and tubal and male factors.

Currently the treatment of choice for IUA is mainly mechanical removal of fibrotic and damaged endometrial tissue using hysteroscopic surgery. Such procedure may provide restoration of anatomical structure without the functional recovery, which leads to limited efficacy in the treatment of infertility caused by repeated embryonic implantation failure. Therefore, development of novel strategies such as the use of biological scaffolds and stem cell therapies are necessary for the treatment of refractory damaged endometrium. However, trials of various potential therapies may raise safety issues when clinically applied. It is also difficult to compare the therapeutic effects among various experimental approaches due to the lack of standardized assessment scales in currently available animal models (Table 1). Hence, the establishment of more compatible animal model to human disease is an essential component of translational research on the recovery of endometrial damage after cell therapy with or without scaffold material (22).

Table 1
Table 1 Currently available animal models with different strain, age, weight, methods for damage, and pregnant status
Full table

Recently, Xu et al. reported a successful establishment of IUA animal model which used pregnant rats. To date, animal models of IUA have been developed using various methods including chemical and/or mechanical injury in non-pregnant animals. The most important cause of IUA seems to be postpartum curettage due to their relationship with this procedure (24). The timing of endometrial trauma in relation to puerperium is considered as one of the most important factors, and this corresponds to the fact that endometrium is recovered within 3 days after curettage in non-pregnant rat models because the hormonal changes associated with pregnancy play a role in inhibiting the regeneration of epithelial cells and promoting fibrosis of interstitial tissue. Therefore, the animal model simulating human IUA using pregnant rats has a great advantage in terms of the similarity of actual pathophysiology of IUA clinically observed.

When establishing IUA animal model in pregnant rats, the procedure of removing multiple embryos in bilateral uterus is added. The shorter the duration of anesthesia is, the better stability and efficiency was shown in production of an IUA animal model (4). Therefore, it would be informative to evaluate how much time was spent by carrying out the procedure of incision, removing embryos and curettage. Also, mechanical methods using curettage were found to show inconsistent degree of damage compared to chemical methods. In this regard, it is necessary to standardize the most efficient protocol of establishing animal models.

Conclusively, since a recent study described a successful establishment of novel IUA animal model, promising results can be expected in regard to the development of more efficient strategy using this animal model.


Acknowledgments

Funding: None.


Footnote

Provenance and Peer Review: This article was commissioned by the editorial office, Annals of Translational Medicine. The article did not undergo external peer review.

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/atm-20-3598). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

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Cite this article as: Kim SW, Kim YY, Kim H, Ku SY. Animal models closer to intrauterine adhesive pathology. Ann Transl Med 2020;8(18):1125. doi: 10.21037/atm-20-3598

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