The human thoracic duct is functionally innervated by adrenergic nerves
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The human thoracic duct is functionally innervated by adrenergic nerves. / Telinius, Niklas; Baandrup, Ulrik; Rumessen, Jüri; Pilegaard, Hans; Hjortdal, Vibeke; Aalkjaer, Christian; Boedtkjer, Donna Briggs.
In: A J P: Heart and Circulatory Physiology (Online), Vol. 306, No. 2, 15.01.2014, p. H206-13.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - The human thoracic duct is functionally innervated by adrenergic nerves
AU - Telinius, Niklas
AU - Baandrup, Ulrik
AU - Rumessen, Jüri
AU - Pilegaard, Hans
AU - Hjortdal, Vibeke
AU - Aalkjaer, Christian
AU - Boedtkjer, Donna Briggs
PY - 2014/1/15
Y1 - 2014/1/15
N2 - Lymphatic vessels from animals have been shown to be innervated. While morphological studies have confirmed human lymphatic vessels are innervated, functional studies supporting this are lacking. The present study demonstrates a functional innervation of the human thoracic duct (TD) that is predominantly adrenergic. TDs harvested from 51 patients undergoing esophageal and cardia cancer surgery were either fixed for structural investigations or maintained in vitro for the functional assessment of innervation by isometric force measurements and electrical field stimulation (EFS). Electron microscopy and immunohistochemistry suggested scarce diffuse distribution of nerves in the entire vessel wall, but nerve-mediated contractions could be induced with EFS and were sensitive to the muscarinic receptor blocker atropine and the α-adrenoceptor blocker phentolamine. The combination of phentolamine and atropine resulted in a near-complete abolishment of EFS-induced contractions. The presence of sympathetic nerves was further confirmed by contractions induced by the sympathomimetic and catecholamine-releasing agent tyramine. Reactivity to the neurotransmitters norepinephrine, substance P, neuropeptide Y, acetylcholine, and methacholine was demonstrated by exogenous application to human TD ring segments. Norepinephrine provided the most consistent responses, whereas responses to the other agonists varied. We conclude that the human TD is functionally innervated with both cholinergic and adrenergic components, with the latter of the two dominating.
AB - Lymphatic vessels from animals have been shown to be innervated. While morphological studies have confirmed human lymphatic vessels are innervated, functional studies supporting this are lacking. The present study demonstrates a functional innervation of the human thoracic duct (TD) that is predominantly adrenergic. TDs harvested from 51 patients undergoing esophageal and cardia cancer surgery were either fixed for structural investigations or maintained in vitro for the functional assessment of innervation by isometric force measurements and electrical field stimulation (EFS). Electron microscopy and immunohistochemistry suggested scarce diffuse distribution of nerves in the entire vessel wall, but nerve-mediated contractions could be induced with EFS and were sensitive to the muscarinic receptor blocker atropine and the α-adrenoceptor blocker phentolamine. The combination of phentolamine and atropine resulted in a near-complete abolishment of EFS-induced contractions. The presence of sympathetic nerves was further confirmed by contractions induced by the sympathomimetic and catecholamine-releasing agent tyramine. Reactivity to the neurotransmitters norepinephrine, substance P, neuropeptide Y, acetylcholine, and methacholine was demonstrated by exogenous application to human TD ring segments. Norepinephrine provided the most consistent responses, whereas responses to the other agonists varied. We conclude that the human TD is functionally innervated with both cholinergic and adrenergic components, with the latter of the two dominating.
KW - Adrenergic Agents/pharmacology
KW - Adrenergic Fibers/drug effects
KW - Aged
KW - Electric Stimulation
KW - Female
KW - Humans
KW - Isometric Contraction
KW - Male
KW - Middle Aged
KW - Sympathetic Nervous System/drug effects
KW - Sympathomimetics/pharmacology
KW - Thoracic Duct/innervation
U2 - 10.1152/ajpheart.00517.2013
DO - 10.1152/ajpheart.00517.2013
M3 - Journal article
C2 - 24213615
VL - 306
SP - H206-13
JO - A J P: Heart and Circulatory Physiology (Online)
JF - A J P: Heart and Circulatory Physiology (Online)
SN - 1522-1539
IS - 2
ER -
ID: 246785288