Key result
Intraspinal reflex circuits orchestrate profound blood pressure changes via eicosanoids interacting with TRP channels.
Why the study?
Spinal sensory reflex control of blood pressure is exaggerated after descending control interruption and may contribute to altered sympathetic input in various disease states.
The spinal cord acts as an integrative center for blood pressure control via viscero-sympathetic reflexes, which are modulated by TRP channels and endogenous eicosanoids.
Answers are grounded in this paper and cite their sources.
Should not yet change blood pressure management; hypothesis-generating for spinal reflex circuits in hypertension.
The spinal cord is an important integrative center for blood pressure control. Spinal sensory fibers send projections to sympathetic preganglionic neurons of the thoracic spinal cord and drive sympathetically-mediated increases in blood pressure. While these reflexes responses occur in able-bodied individuals, they are exaggerated following interruption of descending control – such as occurs following spinal cord injury. Similar reflex control of blood pressure may exist in disease states, other than spinal cord injury, where there is altered input to sympathetic preganglionic neurons. This review primarily focuses on mechanisms wherein visceral afferent information traveling via spinal nerves influences sympathetic nerve activity and blood pressure. There is an abundance of evidence for the widespread presence of this spinal reflex arch originating from virtually every visceral organ and thus having a substantial role in blood pressure control. Additionally, this review highlights specific endogenous eicosanoid species, which modulate the activity of afferent fibers involved in this reflex, through their interactions with transient receptor potential (TRP) cation channels.
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Minić et al. (2022) conducted a review in Blood pressure regulation and spinal cord injury. Intraspinal reflex circuits can directly orchestrate profound reflex-mediated changes in blood pressure, which are modulated by endogenous eicosanoids interacting with transient receptor potential channels.
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