Why the study?
Arteriolar tone regulation is critical for organ blood flow and cardiovascular health, but the interplay and mechanisms by which arteriolar reactivity changes in the presence of multiple vasoactive stimuli required exploration.
How does arteriolar reactivity change in the presence of multiple vasoactive stimuli and by what mechanisms in animal models?
How does arteriolar reactivity change in the presence of multiple vasoactive stimuli and by what mechanisms in animal models?
This scoping review highlights that arteriolar tone regulation involves complex interactions among multiple stimuli, while identifying significant gaps in female animal model research and molecular pathway insights.
Animal data on arteriolar tone regulators may inform mechanistic hypotheses; leaves open human translation and clinical targeting.
BACKGROUND: Cardiovascular diseases remain the leading cause of morbidity and mortality worldwide. Arteriolar tone regulation plays a critical role in maintaining appropriate organ blood flow and perfusion distribution, which is vital for both vascular and overall health. SUMMARY: This scoping review aimed to explore the interplay between five major regulators of arteriolar tone: metabolism (adenosine), adrenergic control (norepinephrine), myogenic activation (intravascular pressure), perivascular oxygen tension, and intraluminal flow rates. Specifically, the aim was to address how arteriolar reactivity changes in the presence of other vasoactive stimuli and by what mechanisms. The review focused on animal studies that investigated the impact of combining two or more of these stimuli on arteriolar diameter. Overall, 848 articles were identified through MEDLINE and EMBASE database searches, and 38 studies were included in the final review. KEY MESSAGES: The results indicate that arteriolar reactivity is influenced by multiple factors, including competitive processes, structural limitations, and indirect interactions among stimuli. Additionally, the review identified a lack of research involving female animal models and limited insight into the interaction of molecular signaling pathways, which represent gaps in the literature.
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Halvorson et al. (2023) studied this question.
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