Literature DB >> 22955058

Responses of neurons in the caudal medullary lateral tegmental field to visceral inputs and vestibular stimulation in vertical planes.

Jennifer D Moy1, Daniel J Miller, Michael F Catanzaro, Bret M Boyle, Sarah W Ogburn, Lucy A Cotter, Bill J Yates, Andrew A McCall.   

Abstract

The dorsolateral reticular formation of the caudal medulla, or the lateral tegmental field (LTF), has been classified as the brain's "vomiting center", as well as an important region in regulating sympathetic outflow. We examined the responses of LTF neurons in cats to rotations of the body that activate vestibular receptors, as well as to stimulation of baroreceptors (through mechanical stretch of the carotid sinus) and gastrointestinal receptors (through the intragastric administration of the emetic compound copper sulfate). Approximately half of the LTF neurons exhibited graviceptive responses to vestibular stimulation, similar to primary afferents innervating otolith organs. The other half of the neurons had complex responses, including spatiotemporal convergence behavior, suggesting that they received convergent inputs from a variety of vestibular receptors. Neurons that received gastrointestinal and baroreceptor inputs had similar complex responses to vestibular stimulation; such responses are expected for neurons that contribute to the generation of motion sickness. LTF units with convergent baroreceptor and vestibular inputs may participate in producing the cardiovascular system components of motion sickness, such as the changes in skin blood flow that result in pallor. The administration of copper sulfate often modulated the gain of responses of LTF neurons to vestibular stimulation, particularly for units whose spontaneous firing rate was altered by infusion of drug (median of 459%). The present results raise the prospect that emetic signals from the gastrointestinal tract modify the processing of vestibular inputs by LTF neurons, thereby affecting the probability that vomiting will occur as a consequence of motion sickness.

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Year:  2012        PMID: 22955058      PMCID: PMC3517700          DOI: 10.1152/ajpregu.00356.2012

Source DB:  PubMed          Journal:  Am J Physiol Regul Integr Comp Physiol        ISSN: 0363-6119            Impact factor:   3.619


  60 in total

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Journal:  Brain Res       Date:  2005-04-07       Impact factor: 3.252

2.  Emetic responses and neural activity in young musk shrews during the breast-feeding/weaning period: comparison between the high and low emetic response strains using a shaking stimulus.

Authors:  Hisao Ito; Mitsuru Nishibayashi; Seishi Maeda; Makoto Seki; Susumu Ebukuro
Journal:  Exp Anim       Date:  2005-07

Review 3.  Central representation of visceral function.

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Journal:  J Neurophysiol       Date:  1988-11       Impact factor: 2.714

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Journal:  Brain Behav Evol       Date:  1983       Impact factor: 1.808

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Journal:  J Neurophysiol       Date:  1976-09       Impact factor: 2.714

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Journal:  Am J Physiol       Date:  1994-06

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Journal:  Behav Brain Res       Date:  1998-06       Impact factor: 3.332

10.  Induction of Fos protein in neurons in the medulla oblongata after motion- and X-irradiation-induced emesis in musk shrews (Suncus murinus).

Authors:  Hisao Ito; Mitsuru Nishibayashi; Keigo Kawabata; Seishi Maeda; Makoto Seki; Susumu Ebukuro
Journal:  Auton Neurosci       Date:  2003-08-29       Impact factor: 3.145

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  11 in total

1.  Hindlimb movement modulates the activity of rostral fastigial nucleus neurons that process vestibular input.

Authors:  Andrew A McCall; Daniel J Miller; Michael F Catanzaro; Lucy A Cotter; Bill J Yates
Journal:  Exp Brain Res       Date:  2015-05-15       Impact factor: 1.972

2.  Responses of vestibular nucleus neurons to inputs from the hindlimb are enhanced following a bilateral labyrinthectomy.

Authors:  Andrew A McCall; Jennifer D Moy; Sonya R Puterbaugh; William M DeMayo; Bill J Yates
Journal:  J Appl Physiol (1985)       Date:  2013-01-10

3.  Vestibular nucleus neurons respond to hindlimb movement in the decerebrate cat.

Authors:  Milad S Arshian; Candace E Hobson; Michael F Catanzaro; Daniel J Miller; Sonya R Puterbaugh; Lucy A Cotter; Bill J Yates; Andrew A McCall
Journal:  J Neurophysiol       Date:  2014-03-26       Impact factor: 2.714

4.  Processing of vestibular inputs by the medullary lateral tegmental field of conscious cats: implications for generation of motion sickness.

Authors:  Andrew A McCall; Jennifer D Moy; William M DeMayo; Sonya R Puterbaugh; Daniel J Miller; Michael F Catanzaro; Bill J Yates
Journal:  Exp Brain Res       Date:  2012-12-29       Impact factor: 1.972

5.  Integration of vestibular and gastrointestinal inputs by cerebellar fastigial nucleus neurons: multisensory influences on motion sickness.

Authors:  Michael F Catanzaro; Daniel J Miller; Lucy A Cotter; Andrew A McCall; Bill J Yates
Journal:  Exp Brain Res       Date:  2014-03-28       Impact factor: 1.972

Review 6.  Vestibulo-sympathetic responses.

Authors:  Bill J Yates; Philip S Bolton; Vaughan G Macefield
Journal:  Compr Physiol       Date:  2014-04       Impact factor: 9.090

7.  Micro RNA 181c-5p: A promising target for post-stroke recovery in socially isolated mice.

Authors:  Maria Antony; Victoria Scranton; Pranay Srivastava; Rajkumar Verma
Journal:  Neurosci Lett       Date:  2019-11-10       Impact factor: 3.046

8.  Effects of visceral inputs on the processing of labyrinthine signals by the inferior and caudal medial vestibular nuclei: ramifications for the production of motion sickness.

Authors:  Milad S Arshian; Sonya R Puterbaugh; Daniel J Miller; Michael F Catanzaro; Candace E Hobson; Andrew A McCall; Bill J Yates
Journal:  Exp Brain Res       Date:  2013-05-28       Impact factor: 1.972

Review 9.  Integration of vestibular and emetic gastrointestinal signals that produce nausea and vomiting: potential contributions to motion sickness.

Authors:  Bill J Yates; Michael F Catanzaro; Daniel J Miller; Andrew A McCall
Journal:  Exp Brain Res       Date:  2014-04-16       Impact factor: 1.972

10.  Responses of neurons in the rostral ventrolateral medulla of conscious cats to anticipated and passive movements.

Authors:  Derek M Miller; Asmita Joshi; Emmanuel T Kambouroglos; Isaiah C Engstrom; John P Bielanin; Samuel R Wittman; Andrew A McCall; Susan M Barman; Bill J Yates
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2020-01-15       Impact factor: 3.619

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