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Delivery of In Vivo Acute Intermittent Hypoxia in Neonatal Rodents to Prime Subventricular Zone-derived Neural Progenitor Cell Cultures
Published on: November 2, 2015
Organismal Responses to Hypoxemic Challenges
Robert S Fitzgerald1, Gholam A Dehghani, Samara Kiihl
1Departments of Environmental Health Sciences, The Johns Hopkins University Medical Institutions, Baltimore, MD, 21205, USA, rfitzger@jhsph.edu.
This study investigated how the body responds to low oxygen. Carotid bodies and aortic bodies, stimulated by hypoxia, trigger sympathetic nervous system responses to maintain blood pressure and organ perfusion.
Area of Science:
- Physiology
- Neuroscience
- Cardiovascular Research
Background:
- The carotid bodies (CBs) and aortic bodies (ABs) are crucial chemoreceptors sensing oxygen levels.
- While their sensing mechanisms are well-studied, organismal reflex responses remain less explored.
Purpose of the Study:
- To investigate the systemic reflex responses to acute hypoxemia mediated by CBs and ABs in cats.
- To differentiate the roles of CBs and ABs in regulating cardiovascular and organ vascular resistance during hypoxia.
Main Methods:
- Cats were subjected to hypoxic hypoxia (HH) and carbon monoxide hypoxia (COH) to selectively stimulate CBs and ABs.
- Whole animal responses (cardiac output, blood pressure) and regional vascular resistance (brain, heart, spleen, etc.) were recorded.
- Aortic depressor nerves were sectioned to isolate the contribution of CBs.
Main Results:
- Hypoxic hypoxia (HHint) effectively maintained perfusion pressures during systemic hypoxemia.
- CBs mediated vasodilation in adrenals and eyes, while spleen and pancreas showed vasoconstriction.
- Aortic bodies significantly influenced pulmonary vasculature and stomach blood flow.
Conclusions:
- The sympathetic nervous system, activated by chemoreceptors, plays a primary role in the organism's hypoxemia response.
- CBs and ABs exert differential effects on organ-specific vascular resistance.
- This study highlights the integrated reflex control of circulation during hypoxic stress.
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