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DOI 10.1177/11297298211026083

Медицинская библиотека · The journal of vascular access · 2021

Cardiac changes following arteriovenous fistula creation in a mouse model.

Ingle Kevin, Pham Linh, Lee Viangkaeo, Guo Lingling, Isayeva-Waldrop Tatyana, Somarathna Maheshika, Lee Timmy

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Аннотация

BACKGROUND

Arteriovenous fistula (AVF) creation may negatively affect cardiac structure and function and impact cardiovascular mortality. The objective of this study was to develop and characterize the cardiac changes following AVF creation in a murine AVF model.

METHODS

AVFs were constructed using the carotid artery and jugular vein in C57BL/6 mice. Sham-operated AVF mice served as the control group. 2D-echocardiography was performed prior to AVF creation (baseline) and at 7 and 21 days after creation in AVF and sham-operated mice. Picrosirius red was used to stain the left ventricle for collagen production.

RESULTS

The cardiac output (CO), left ventricular end diastolic (LVEDD) and systolic (LVESD) diameter, and end-diastolic (LVEDV) and systolic (LVESV) volume was significantly increased at 7 and 21 days in AVF compared to sham-operated mice. There was also a significant increase in CO, LVEDD, LVESD, LVEDV, and LVESV from baseline to 21 days within the AVF group, but not the sham-operated mice. There was a significant decrease in ejection fraction and fractional shortening at 21 days in AVF compared to sham-operated mice. Picrosirius red was significantly more prominent around both the perivascular and interstitial areas of the cardiac tissue from AVF mice compared to sham-operated AVF mice at 21 days.

CONCLUSIONS

The creation of an AVF in our murine model leads to cardiac changes such as increased cardiac output, left ventricular dilation, and cardiac fibrosis, while showing reductions of ejection fraction and fractional shortening.

Для цитирования: Ingle Kevin, Pham Linh, Lee Viangkaeo, Guo Lingling, Isayeva-Waldrop Tatyana, Somarathna Maheshika, Lee Timmy. Cardiac changes following arteriovenous fistula creation in a mouse model.. The journal of vascular access. 2021. DOI: 10.1177/11297298211026083.

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