Literature DB >> 7845592

Distribution of cholinergic, GABAergic and serotonergic neurons in the medial medullary reticular formation and their projections studied by cytotoxic lesions in the cat.

C J Holmes1, L S Mainville, B E Jones.   

Abstract

As part of a larger study concerning the role of neurons in the medial medullary reticular formation in sleep-wake states, the distribution and projections of cholinergic, GABAergic and serotonergic neurons were studied within the lower brainstem of the cat. Cells were plotted with the aid of an image analysis system through the medullary reticular formation and raphe in adjacent sections immunostained for choline acetyltransferase, glutamic acid decarboxylase and serotonin. Immunostained fibres and varicosities were examined and quantified by microdensitometry in regions of the medulla, pons and upper spinal cord in normal and quisqualate-injected animals to assess the loss of local and distant projections following cytotoxic destruction of neurons in the medial medullary reticular formation. Choline acetyltransferase-immunoreactive neurons are unevenly and sparsely distributed, though none the less in significant numbers (estimated at approximately 9080 in total), through the medial medullary reticular formation, and are present in all tegmental fields, including the gigantocellular (approximately 3700) and magnocellular (approximately 1760) rostrally and the ventral (approximately 3240) and paramedian (approximately 380) caudally, and are absent in the midline raphe. Glutamic acid decarboxylase-immunoreactive neurons are more evenly and densely distributed in large numbers (estimated at approximately 18,720) through the medial medullary reticular formation, being present in the gigantocellular (approximately 5960), magnocellular (approximately 8260), ventral (approximately 2280) and paramedian (approximately 2220) tegmental fields, and are also numerous within the raphe magnus and pallidus-obscurus nuclei (approximately 3880). Serotonin-immunoreactive cells are sparse in the medial medullary reticular formation (estimated to total approximately 1540), where they are mainly located in the magnocellular tegmental field (approximately 1340), and are concentrated in larger numbers within the raphe nuclei (approximately 8060). Cholinergic varicose fibres were moderately densely distributed through the medial medullary reticular formation, as well as through more distant lateral, rostral and caudal brainstem and upper spinal regions. After cytotoxic lesions focussed in the gigantocellular and magnocellular tegmental fields, a loss of approximately 55% of the cholinergic neurons in the medial medullary reticular formation was associated with a minor decrease (approximately 35% in optical density measures) of local cholinergic fibres. Small and variable reductions in varicose fibres (and their optical density measures) were detected in distant structures (including the pontine lateral, gigantocellular and subcoerular tegmental fields and the caudal spinal trigeminal nucleus), that were none the less correlated with the number of intact medial medullary cholinergic cells, suggesting that these cells may project to distant brainstem targets, in addition to providing a minor proportion of the local cholinergic innervation of the medial medullary reticular formation.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 7845592     DOI: 10.1016/0306-4522(94)90351-4

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  27 in total

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Authors:  M A Parkis; X Dong; J L Feldman; G D Funk
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2.  Arousal from sleep in response to intermittent hypoxia in rat pups is modulated by medullary raphe GABAergic mechanisms.

Authors:  Robert A Darnall; Robert W Schneider; Christine M Tobia; Benjamin M Zemel
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2011-12-07       Impact factor: 3.619

3.  A quantitative study of the brainstem cholinergic projections to the ventral part of the oral pontine reticular nucleus (REM sleep induction site) in the cat.

Authors:  Margarita Lucía Rodrigo-Angulo; Elisia Rodríguez-Veiga; Fernando Reinoso-Suárez
Journal:  Exp Brain Res       Date:  2004-09-10       Impact factor: 1.972

4.  The brainstem reticular formation is a small-world, not scale-free, network.

Authors:  M D Humphries; K Gurney; T J Prescott
Journal:  Proc Biol Sci       Date:  2006-02-22       Impact factor: 5.349

5.  Effects of electrical stimulation of the medullary raphe nuclei on respiratory movement in rats.

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Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2006-01-11       Impact factor: 1.836

6.  Is there a brainstem substrate for action selection?

Authors:  M D Humphries; K Gurney; T J Prescott
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2007-09-29       Impact factor: 6.237

7.  Supraspinal respiratory plasticity following acute cervical spinal cord injury.

Authors:  Tatiana Bezdudnaya; Vitaliy Marchenko; Lyandysha V Zholudeva; Victoria M Spruance; Michael A Lane
Journal:  Exp Neurol       Date:  2017-04-19       Impact factor: 5.330

8.  Focal CO2 dialysis in raphe obscurus does not stimulate ventilation but enhances the response to focal CO2 dialysis in the retrotrapezoid nucleus.

Authors:  Mirela Barros Dias; Aihua Li; Eugene Nattie
Journal:  J Appl Physiol (1985)       Date:  2008-05-01

9.  State-dependent control of lumbar motoneurons by the hypocretinergic system.

Authors:  Jack Yamuy; Simon J Fung; Mingchu Xi; Michael H Chase
Journal:  Exp Neurol       Date:  2009-12-03       Impact factor: 5.330

10.  Sensory Cortical Activity Is Related to the Selection of a Rhythmic Motor Action Pattern.

Authors:  Jennifer X Li; Joost X Maier; Emily E Reid; Donald B Katz
Journal:  J Neurosci       Date:  2016-05-18       Impact factor: 6.167

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