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Article type: Research Article
Authors: Yang, Lua | Mo, Liquna | Li, Fuyua | Zhu, Fuzua | Bai, Yipinga; b; *
Affiliations: [a] Department of Anesthesiology, Affiliated Hospital of Southwest Medical University, Luzhou, China | [b] Anesthesiology and Critical Care Medicine Key Laboratory of Luzhou, Luzhou, China
Correspondence: [*] Corresponding author: Yiping Bai, Department of Anesthesiology, Affiliated Hospital of Southwest Medical University, Luzhou, China. E-mail: baiyiping0608@163.com.
Abstract: BACKGROUND & OBJECTIVE:We aimed to evaluate the effect of sitaxentan on renal microvascular perfusion via application of ultrasound microbubble contrast. METHODS:Male beagles were randomly divided into: Sham, cardiopulmonary bypass (CPB) and sitaxentan-infused (Sit) groups (n = 6). The ascending slope rate (ASR), area under the curve (AUC), derived peak intensity, and time to peak (TTP) were obtained via ultrasound microbubble contrast before CPB (T1), after 1 h CPB (T2), at end of CPB (T3), and 2 h after CPB (T4). RESULTS:Compared with the Sham group, the CPB group had lower ASR of the renal cortex and medulla at T2 - 4, higher AUC and TTP at T3 - 4, and lower derived peak intensity at T4. The ASR at T2 - 4 in the Sit group was lower, TTP was higher at T2 - 4, and AUC was higher at T3 - 4 (P < 0.05). Compared with the CPB group, the Sit group had higher ASR of the renal cortex and medulla at T3 - 4 and AUC and TTP at T3 - 4 (P < 0.05). Compared with that at T1, the ASR of the renal cortex and medulla at T2 - 4 in the CPB group was lower, and AUC and TTP were higher at T3 - 4. The ASR of the renal cortex and medulla at T2 - 4 in the Sit group was lower, TTP was higher at T2 - 4, and AUC was higher at T4 (P < 0.05). CONCLUSIONS:Ultrasound microbubble contrast could be effectively used to evaluate renal microvascular perfusion peri-CPB in beagles, which was prone to decrease and could be improved via pretreatment with sitaxentan.
Keywords: Ultrasound, kidney, microcirculation, cardiopulmonary bypass, endothelin receptor antagonist
DOI: 10.3233/CH-221600
Journal: Clinical Hemorheology and Microcirculation, vol. 85, no. 2, pp. 115-121, 2023
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