Why the study?
Does tissue ACE contribute to imposed and physiological flow-related arterial remodeling in mice?
Does tissue ACE contribute to imposed and physiological flow-related arterial remodeling in mice?
Tissue ACE is crucial for hyperplastic inward remodeling following blood flow cessation but not for physiological remodeling of uterine arteries during pregnancy.
Tissue ACE contributes to pathological arterial remodeling in mice; leaves open relevance to human vascular disease or therapy.
OBJECTIVE: To test whether membrane-bound angiotensin I-converting enzyme (t-ACE) is involved in arterial remodeling, we applied unilateral carotid artery (CA) ligation and studied uterine arteries (UA) before, during, and after pregnancy in t-ACE-/- and t-ACE+/+ mice. RESULTS- In CA of t-ACE-/- mice, blood pressure, outer diameter (D), and medial cross-sectional area (mCSA) were reduced, whereas blood flow (BF) and the number of medial cells (mC) were not modified. In the ligated CA, mCSA and number of mC were increased while outer D and distensibility were reduced. These changes were significantly less pronounced in t-ACE-/- than t-ACE+/+ mice. In UA of t-ACE-/- mice, D was larger and mCSA was unaltered. At term pregnancy, D and mCSA of the UA were reversibly increased. Structural changes of UA during and after pregnancy were comparable in both strains. CONCLUSIONS: t-ACE contributes to arterial structure and remodeling. It plays a major role in hyperplastic inward remodeling of the CA imposed by blood flow cessation, but it is not essential for outward hypertrophic and subsequent inward hypotrophic remodeling of the UA during and after pregnancy.
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Hilgers et al. (2004) studied this question.
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