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Lovering, Andrew T

0000-0001-7826-4290

Mayo Clinic

Department of Human Physiology, University of Oregon, Eugene, Oregon, United States.

Citations 3

Reduction in respiratory muscle strength following a series of preparatory and maximal static, dry breath-holds
Hubbard, Colin D. , Vrdoljak, Dario , Cross, Troy J. , Lovering, Andrew T. , Drviš, Ivan, Dujić, Željko , Foretić, Nikola , Duke, Joseph W. , Coombs, Geoff B , Cross, Troy James , Taylor, Bryan J , Lovering, Andrew T , Dujić, Željko , Foretić, Nikola , Duke, Joseph W , Hubbard, Colin D. , Taylor, Bryan J.

Journal of Applied Physiology | October 3, 2025 | Volume: 139 | Issue: 5 | Pages: 1235-1245

10.1152/japplphysiol.00256.2025 Get It

Respiratory muscle fatigue could occur following involuntary breathing movements during maximal breath-holds. We measured respiratory muscle strength pre and post three preparatory and maximal breath-holds. We found significant reductions in diaphragm strength and total inspiratory and expiratory strength in some, but not all, divers. Divers that had respiratory muscle fatigue had a lower pseudo O 2 delivery (HR × [Formula: see text]) during the struggle phase. This suggests that reduced oxygen delivery may contribute to respiratory muscle fatigue during a breath-hold.
Clinical Consideration for Techniques to Detect and Quantify Blood Flow through Intrapulmonary Arteriovenous Anastomoses: Lessons from Physiological Studies
Duke, Joseph W. , Elliott, Jonathan E. , Lovering, Andrew T. , Elliott, Jonathan E , Lovering, Andrew T

Echocardiography | February 19, 2015 | Volume: 32 | Issue: S3 | Pages: No page available

10.1111/echo.12839 Get It

Intrapulmonary arteriovenous anastomoses (IPAVA) are large diameter (>50 μm) vascular conduits, present in >95% of healthy humans. Because IPAVA are large diameter pathways that allow blood flow to bypass the pulmonary capillary network, blood flow through IPAVA (QIPAVA) can permit the transpulmonary passage of particles larger than pulmonary capillaries. IPAVA have been known to exist for over 50 years, but their physiological and clinical significance are still being established; although, currently suggested roles for QIPAVA include allowing emboli to reach the systemic circulation and providing a source of shunt. Studying QIPAVA is an important area of research and as the suggested roles become better established, detecting and quantifying QIPAVA may become significantly more important in the clinic. Several techniques that can be used to quantify and/or detect QIPAVA in animals, ex vivo human/animal lungs, and intact healthy humans; microspheres, radiolabeled macroaggregated albumin particles, and saline contrast echocardiography, are reviewed with limitations and advantages to each. The current body of literature using these techniques to study QIPAVA in animals, ex vivo lungs, and healthy humans has established conditions when QIPAVA is present, such as during exercise or with arterial hypoxemia and conditions when QIPAVA is absent, such as at rest or during exercise breathing 100% O2. Many of these physiological studies have direct application to patient populations and we discuss each of these findings in the context of their potential to influence the clinical utility, and interpretation, of the results from these techniques highlighted in this review.
Intrapulmonary arteriovenous anastomoses in humans – response to exercise and the environment
Lovering, Andrew T. , Duke, Joseph W. , Elliott, Jonathan E. , Elliott, Jonathan E , Lovering, Andrew T

The Journal of Physiology | December 12, 2014 | Volume: 593 | Issue: 3 | Pages: 507-520

10.1113/jphysiol.2014.275495 Get It

AbstractIntrapulmonary arteriovenous anastomoses (IPAVA) have been known to exist in human lungs for over 60 years. The majority of the work in this area has largely focused on characterizing the conditions in which IPAVA blood flow (IPAVA) is either increased, e.g. during exercise, acute normobaric hypoxia, and the intravenous infusion of catecholamines, or absent/decreased, e.g. at rest and in all conditions with alveolar hyperoxia ( = 1.0). Additionally, IPAVA is present in utero and shortly after birth, but is reduced in older (>50 years) adults during exercise and with alveolar hypoxia, suggesting potential developmental origins and an effect of age. The physiological and pathophysiological roles of IPAVA are only beginning to be understood and therefore these data remain controversial. Although evidence is accumulating in support of important roles in both health and disease, including associations with pulmonary arterial pressure, and adverse neurological sequelae, there is much work that remains to be done to fully understand the physiological and pathophysiological roles of IPAVA. The development of novel approaches to studying these pathways that can overcome the limitations of the currently employed techniques will greatly help to better quantify IPAVA and identify the consequences of IPAVA on physiological and pathophysiological processes. Nevertheless, based on currently published data, our proposed working model is that IPAVA occurs due to passive recruitment under conditions of exercise and supine body posture, but can be further modified by active redistribution of pulmonary blood flow under hypoxic and hyperoxic conditions.