Decreased carotid arterial resistance in cats in response to trigeminal stimulation

Geoffrey A. Lambert Department of Neurology, The Prince Henry Hospital Little Bay, and School of Medicine, University of New South Wales, Sydney, Australia

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 Ph.D.
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Nikolai Bogduk Department of Neurology, The Prince Henry Hospital Little Bay, and School of Medicine, University of New South Wales, Sydney, Australia

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 Ph.D., M.B., B.S.
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Peter J. Goadsby Department of Neurology, The Prince Henry Hospital Little Bay, and School of Medicine, University of New South Wales, Sydney, Australia

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John W. Duckworth Department of Neurology, The Prince Henry Hospital Little Bay, and School of Medicine, University of New South Wales, Sydney, Australia

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James W. Lance Department of Neurology, The Prince Henry Hospital Little Bay, and School of Medicine, University of New South Wales, Sydney, Australia

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 M.D.
Page Range:
307–315
Volume/Issue:
Volume 61: Issue 2
DOI link:
https://doi.org/10.3171/jns.1984.61.2.0307
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✓ Stimulation of the trigeminal nerve or ganglion in the cat caused a frequency-dependent reduction in carotid vascular resistance. Systemic arterial blood pressure (SABP) decreased at low frequencies (0.2 to 5 sec−1) and increased at higher frequencies, thus increasing carotid blood flow at the higher frequencies. The effect on resistance was predominantly ipsilateral and was unaltered by cervical sympathectomy, but was abolished or substantially reduced by section of the trigeminal root proximal to the ganglion. Diminution of carotid vascular resistance was replicated by stimulation of the greater superficial petrosal (GSP) nerve without any change in SABP. Section of the seventh cranial nerve reduced or abolished the response to stimulation of the trigeminal nerve but not that from the GSP nerve. The trigeminal response was prevented by ganglion-blocking drugs in seven out of eight cats. The resistance response was unaffected by noradrenergic, cholinergic, serotonergic, and histamine-2 blocking agents. No neural connection could be demonstrated between the GSP and the trigeminal ganglion, and the vascular response to GSP stimulation persisted after trigeminal section. It is concluded that activation of the trigeminal system increases carotid blood flow by a pathway involving the seventh cranial nerve, the GSP and Vidian nerves, and a parasympathetic synapse employing an unconventional transmitter. A varying proportion of the response (greatest in the third division) may be mediated by antidromic activation of trigeminal nerves. These findings may have clinical implications for the vascular changes of migraine and other facial pain.

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Contributor Notes

Address reprint requests to: Geoffrey A. Lambert, M.D., Department of Neurology, Clinical Sciences Building, The Prince Henry Hospital, Little Bay, New South Wales 2036, Australia.
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