Key result
Chronic hypoxia linked to reduced endothelial-dependent dilation, an effect fully reversed by adrenergic blockade.
Why the study?
Chronic hypoxia is associated with elevated sympathetic activity and reduced vascular function, but the mechanistic link between chronically elevated sympathetic nervous activity and hypoxia-induced vascular dysfunction has not been determined.
Does local α+β adrenergic receptor blockade improve endothelial-dependent dilation in lowlanders exposed to chronic hypoxia and Andean highlanders with excessive erythrocytosis?
Observational (n=24)
Does local α+β adrenergic receptor blockade improve endothelial-dependent dilation in lowlanders exposed to chronic hypoxia and Andean highlanders with excessive erythrocytosis?
Heightened α-adrenergic signaling impairs endothelial function during chronic exposure to hypobaric hypoxia, and adrenergic blockade can restore this function.
Answers are grounded in this paper and cite their sources.
Adrenergic blockade may restore endothelial dilation impaired by chronic hypoxia; hypothesis-generating for targeted therapy in hypoxic conditions.
Rationale: Chronic exposure to hypoxia is associated with elevated sympathetic nervous activity and reduced vascular function in lowlanders, and Andean highlanders suffering from excessive erythrocytosis (EE); however, the mechanistic link between chronically elevated sympathetic nervous activity and hypoxia-induced vascular dysfunction has not been determined. Objective: To determine the impact of heightened sympathetic nervous activity on resistance artery endothelial-dependent dilation (EDD), and endothelial-independent dilation, in lowlanders and Andean highlanders with and without EE. Methods and Results: We tested healthy lowlanders (n=9) at sea level (344 m) and following 14 to 21 days at high altitude (4300 m), and permanent Andean highlanders with (n=6) and without (n=9) EE at high altitude. Vascular function was assessed using intraarterial infusions (3 progressive doses) of acetylcholine (ACh; EDD) and sodium nitroprusside (endothelial-independent dilation) before and after local α+β adrenergic receptor blockade (phentolamine and propranolol). Intraarterial blood pressure, heart rate, and simultaneous brachial artery diameter and blood velocity were recorded at rest and during drug infusion. Changes in forearm vascular conductance were calculated. The main findings were (1) chronic hypoxia reduced EDD in lowlanders (changes in forearm vascular conductance from sea level: ACh1: −52.7±19.6%, ACh2: −25.4±38.7%, ACh3: −35.1±34.7%, all P ≤0.02); and in Andeans with EE compared with non-EE (changes in forearm vascular conductance at ACh3: −36.4%, P =0.007). Adrenergic blockade fully restored EDD in lowlanders at high altitude, and normalized EDD between EE and non-EE Andeans. (2) Chronic hypoxia had no effect on endothelial-independent dilation in lowlanders, and no differences were detected between EE and non-EE Andeans; however, EID was increased in the non-EE Andeans after adrenergic blockade ( P =0.012), but this effect was not observed in the EE Andeans. Conclusions: These data indicate that chronic hypoxia reduces EDD via heightened α-adrenergic signaling in lowlanders and in Andeans with EE. These vascular mechanisms have important implications for understanding the physiological consequences of acute and chronic high altitude adaptation.
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Tymko et al. (2020) conducted an observational in Chronic exposure to hypobaric hypoxia and excessive erythrocytosis (n=24). Local α+β adrenergic receptor blockade (phentolamine and propranolol) vs. Baseline (sea level for lowlanders, non-EE for Andeans) was evaluated on Endothelial-dependent dilation (EDD) and endothelial-independent dilation (p=≤0.02). Chronic hypoxia reduced endothelial-dependent dilation in lowlanders (P≤0.02) and Andeans with excessive erythrocytosis (P=0.007), an effect fully restored by adrenergic blockade.
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