Literature DB >> 7272762

A quantitative study of the effects of early unilateral olfactory deprivation on the number and distribution of mitral and tufted cells and of glomeruli in the rat olfactory bulb.

E Meisami, L Safari.   

Abstract

Anatomic effects of early unilateral olfactory deprivation on the developing olfactory bulb were investigated in the albino rat. Unilateral anosmia was experimentally induced by neonatal cauterization of the left or right nare; regenerating the tissue permanently blocked the nostril. The anosmic olfactory bulb (ipsilateral to the blocked nare) and its contralateral counterpart, serving as the normal control, were compared for the following quantitative anatomic parameters: total number and distribution of mitral and tufted cells and olfactory glomeruli; average diameters of mitral cells and glomeruli; relative dimensions of the bulb and its layers. The effects on mitral cells and glomeruli were studied at the ages of 25 and 60 days and at 2 years; other studies were carried out in the 25-day-old animals only. In the normal mature bulb, the number of mitral cells, tufted cells and glomeruli was found to be about 70,000, 160,000 and 3000, respectively. It was found that the absence of early olfactory stimulation was invariably correlated with a significant and permanent loss of mitral cells, amounting to more than a quarter of the total number. This loss apparently occurred rapidly during the first 3 weeks, as it was already evident by day 25 and did not increase appreciably with prolongation of deprivation. Tufted cells were apparently even more susceptible, because their number decreased by about 45%. As evident from this distribution profiles, the loss of mitral and tufted cells occurred uniformly throughout the bulb. It is shown that these differences were due neither to inherent interbulbar differences, nor to a hyperplasia in the normal bulb. Early anosmia had no significant effects on the number or average diameter of the glomeruli. Morphometric studies revealed that the dimensions and thickness of layers (internal and external plexiform and granular) of the anosmic bulb were significantly reduced. It is suggested that early olfactory stimulation is necessary for survival of the developing mitral and tufted cells; thus the first 2-3 postnatal weeks, covering the final developmental stages of these cells, would constitute a vulnerable period in the development of the rat olfactory system.

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Year:  1981        PMID: 7272762     DOI: 10.1016/0006-8993(81)91065-9

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  20 in total

1.  Long-lasting depolarizations in mitral cells of the rat olfactory bulb.

Authors:  G C Carlson; M T Shipley; A Keller
Journal:  J Neurosci       Date:  2000-03-01       Impact factor: 6.167

2.  Spontaneous field potentials in the glomeruli of the olfactory bulb: the leading role of juxtaglomerular cells.

Authors:  S V Karnup; A Hayar; M T Shipley; M G Kurnikova
Journal:  Neuroscience       Date:  2006-07-28       Impact factor: 3.590

3.  Deafferentation-induced alterations in mitral cell dendritic morphology in the adult zebrafish olfactory bulb.

Authors:  Joanna M Pozzuto; Cynthia L Fuller; Christine A Byrd-Jacobs
Journal:  J Bioenerg Biomembr       Date:  2018-09-13       Impact factor: 2.945

4.  Lithium increases bcl-2 expression in chick cochlear nucleus and protects against deafferentation-induced cell death.

Authors:  A L Bush; R L Hyson
Journal:  Neuroscience       Date:  2006-01-18       Impact factor: 3.590

5.  The D2 antagonist spiperone mimics the effects of olfactory deprivation on mitral/tufted cell odor response patterns.

Authors:  D A Wilson; R M Sullivan
Journal:  J Neurosci       Date:  1995-08       Impact factor: 6.167

6.  Investigation of the role of interneurons and their modulation by centrifugal fibers in a neural model of the olfactory bulb.

Authors:  C Linster; R Gervais
Journal:  J Comput Neurosci       Date:  1996-09       Impact factor: 1.621

Review 7.  Determination of the connectivity of newborn neurons in mammalian olfactory circuits.

Authors:  Namasivayam Ravi; Luis Sanchez-Guardado; Carlos Lois; Wolfgang Kelsch
Journal:  Cell Mol Life Sci       Date:  2016-09-30       Impact factor: 9.261

8.  Effects of reversible nare occlusion on the development of the olfactory epithelium in the rabbit nasal septum.

Authors:  B Stahl; H Distel; R Hudson
Journal:  Cell Tissue Res       Date:  1990-02       Impact factor: 5.249

9.  Kv1.3 channel gene-targeted deletion produces "Super-Smeller Mice" with altered glomeruli, interacting scaffolding proteins, and biophysics.

Authors:  D A Fadool; K Tucker; R Perkins; G Fasciani; R N Thompson; A D Parsons; J M Overton; P A Koni; R A Flavell; L K Kaczmarek
Journal:  Neuron       Date:  2004-02-05       Impact factor: 17.173

10.  The influence of chronic lithium administration on deafferentation-induced cellular changes in the chick cochlear nucleus.

Authors:  A L Bush; K L Carzoli; R L Hyson
Journal:  Neuroscience       Date:  2008-09-09       Impact factor: 3.590

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