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M Achaval

Publications and source records attributed to M Achaval.

At least 37 records · Page 2Linked to original sources
PubMed1997

GMP protects against quinolinic acid-induced loss of NADPH-diaphorase-positive cells in the rat striatum.

When injected into the rat striatum, quinolinic acid causes dose-dependent widespread cell death. All cell types, including the NADPH-diaphorase-positive neurons appear to be sensitive to the toxin. The latter cells are destroyed by quinolinic acid injections of 180 nmol per striatum, this effect being blocked by the concomitant administration of 5 mg/kg of the non-competitive N-methyl-D-aspartate antagonist MK-801. We report that guanosine-5'-monophosphate (GMP), at a dose of 360 nmol, is equally effective in protecting the diaphorase-positive cells against quinolinate toxicity.

Animals↗
PubMed1995

Brain and respiratory cilia: the effect of temperature.

We have used a modified photodiode method to measure ciliary beat frequency of human neonatal cilia, and have developed techniques to allow similar measurements of rat brain cilial function. The effect of temperature change, within the physiological range, on neonatal human respiratory cilia and neonatal rat brain cilia was studied. The mean (SD) ciliary beat frequency of neonatal respiratory cilia at body temperature was 14 (1.1) Hz and that of rat brain cilia 18.9 (1.3) Hz. Respiratory cilial beat frequency decreased by 9.1% and brain cilia by 13% on cooling to 32 degrees C compared to normal body temperature. Beat frequency increased by 8.5% in respiratory samples and by 12% in brain samples on warming to 40 degrees C compared to the frequency at normal body temperature. The Q10 of human neonatal respiratory cilia was 1.2 and that of rat brain cilia 1.3.

Animals↗
PubMed1991

Lasting loss in substance P following administration of substance P antiserum to newborn rats. An immunohistochemical study.

Substance P (SP) antiserum (500 micrograms protein) was administered to rats on the second day of life and the animals were sacrificed 3 months later. This treatment produced a loss in SP immunoreactive fibers in the dorsal horn of the spinal cord, in the substantia nigra and in the periaqueductal gray matter, when compared to control animals receiving a neonatal treatment of non-specific immunoglobulins. In the dorsal horn, the observed depletion was greater in the superficial layers, lamina I and lamina IIo. Immunoreactivity for Met-enkephalin was apparently unchanged by SP antiserum. Results of this study provide cytochemical evidence for a specific and lasting deleterious effect of SP antiserum on different SP-containing neuronal systems.

Animals↗
PubMed1991

Subcellular localization of nerve growth factor receptors in identified cells of the rat nucleus basalis magnocellularis: an immunocytochemical study.

The subcellular location of nerve growth factor receptor in the ventromedial portion of rat globus pallidus was investigated with affinity-purified monoclonal 192-IgG following the unlabelled antibody peroxidase-antiperoxidase immunocytochemical procedure. At the light microscopic level, punctate immunoreaction product was observed in the perinuclear region and in the plasma membrane of large, probably cholinergic neurons. Examination in the electron microscope of these neurons confirmed that nerve growth factor receptor-stained cells were basal forebrain cholinergic neurons. Within these cells, immunostaining occurred in the Golgi apparatus, in multivesicular bodies and, occasionally, in rough endoplasmic reticulum cisternae and the nuclear envelope. Moreover, patches of immunoreactivity were observed associated with the outer surface of the plasma membrane of the soma and their proximal dendrites and also with the plasma membrane of distal dendrites showing scarcity of synaptic input. Positive immunostaining was never observed in synaptic clefts, but filled the space between the plasma membranes of immunoreactive neurons and those of thin glial processes in their vicinity. The location of membrane nerve growth factor receptor in close apposition to membranes of neighbouring astrocytes rather than near synaptic complexes, suggests that glial cells may be a physiological source of nerve growth factor.

Animals↗
PubMed1991

Molecular pathways of pain: Fos/Jun-mediated activation of a noncanonical AP-1 site in the prodynorphin gene.

Noxious stimulation provokes the activation of genes that are thought to play a crucial role in the phenomena of stress and pain. Among these is the prodynorphin gene. By double-labeling in situ hybridization/immunohistochemistry, we show that increased prodynorphin gene expression is preceded, in the same neurons, by an early induction of c-fos. Inspection of the prodynorphin promoter region revealed the presence of several AP-1-like sequences. We demonstrate that only one of these sites is a functional AP-1 element. It is constituted by the noncanonical TGACAAACA sequence, in which the palindromic structure is partly conserved by the 3' terminal CA dinucleotide. Transfection experiments in NCB20 neuroblastoma cells indicated that this site is a target of Fos/Jun trans-activation. Our results suggest that Fos/Jun oncoproteins may function as third messengers in the signal transduction mechanisms of stress/pain processes.

Amino Acid Sequence↗
PubMed1991

Differential expression of the jun family members in rat brain.

The transcription factor AP-1 is phorbol ester-regulated and, as such, is considered to be a nuclear target of the signal transduction pathway involving protein kinase C. AP-1 is constituted by the various products of the jun and fos gene family members. These genes belong to the early response class and are inducible in different ways by growth factors, phorbol esters and depolarization. We studied the transcript distribution of c-jun, junB and junD in the rat brain. Our results show that the transcripts for these three genes are differentially distributed in various neuronal tissues. We also provide evidence for developmentally regulated expression of jun genes in post-natal brain. The spatiotemporal pattern of expression of c-jun, junB and junD offers clues to the understanding of the links between gene regulation and neuronal processes.

Aging↗
PubMed1991

Co-induction of jun B and c-fos in a subset of neurons in the spinal cord.

Noxious stimulation in vivo provokes the transcriptional activation of several genes which are thought to play an important role in the phenomena of stress and pain. In the rat, the expression of the c-fos proto-oncogene is rapidly induced upon noxious stimulation in defined neurons in the dorsal horn of the spinal cord. Interestingly, expression of the prodynorphin gene, which is thought to be involved in the endogenous mechanisms for pain/stress control, also localizes in the same anatomical area. Fos proteins are known to associate in transcriptional complexes with the products of the jun family constituting nuclear factor AP-1. These considerations prompted us to analyse the expression of the jun gene family members c-jun, jun B and jun D in rats subjected to noxious stimulation. We present data indicating that in unstimulated animals the transcripts of the three genes are differentially expressed and abundant within the various laminas of the lumbar spinal cord. Surprisingly, upon stimulation only the jun B transcript is augmented, being co-localized with Fos in a subset of neurons of the medial dorsal horn.

Animals↗
PubMed1989

Localization of C-PON immunoreactivity in the rat main olfactory bulb. Demonstration that the population of neurons containing endogenous C-PON display NADPH-diaphorase activity.

The presence of the neuropeptide C-terminal flanking peptide of neuropeptide-Y, C-PON, has been investigated in the main olfactory bulb of the rat using conventional fluorescence and peroxidase-antiperoxidase immunocytochemical techniques. The distribution of immunoreactive structures to C-PON was examined in both horizontal and coronal sections. Endogenous C-PON was localized within two types of short-axon cells including (1) superficial short-axon cells in the glomerular layer and (2) deep short-axon cells lying in the deepest portion of the granule cell layer and in the adjacent white matter. In addition, varicose immunoreactive processes were detected in all layers, although they were more numerous in the deepest portion of the granule cell layer. Immunoreactive cell bodies and processes were also observed in the nucleus olfactorius anterior and in the intrabulbar portion of the anterior commissure. Nevertheless, immunoreactive structures were not localized in the lateral olfactory tract. The indirect immunofluorescence technique to detect endogenous C-PON in combination with the enzyme histochemical demonstration of NADPH-diaphorase activity, in single sections, showed that the NADPH-diaphorase procedure is a reliable marker for these C-PON positive cells. Also, indirectly, that, in the rat main olfactory bulb, C-PON and neuropeptide-Y are contained in the same cell types. Many glomeruli were stained following the NADPH-diaphorase procedure, but they were not C-PON immunoreactives. Results of this study provide evidence suggesting that C-PON may influence polysynaptically the function of mitral cells and, therefore, the olfactory bulb output.

Animals↗
PubMed1986

Acetylcholinesterase activity during the ontogenesis of the subfornical organ of the rat.

From 16 to 18 days of fetal life (fl) the subfornical organ (SFO) of the rat shows diffuse acetylcholinesterase (AChE) activity. From 21 fl its definitive pattern begins to be organized and is achieved at 30 days of postnatal life (pl). This pattern is characterized by a homogeneous AChE activity in the rostral region, a ring-like distribution in the anterior medial region and a hoof-like distribution in the posterior medial region. The caudal region shows intense, uniform activity. From the rostral region two tracts emerge, ventral and dorsal, that extend to different diencephalo-telencephalic areas. From the SFO caudal region another tract emerges that extends to posterior areas.

Acetylcholinesterase↗
PubMed1984

Topographical distribution of acetylcholinesterase in the subfornical organ of the rat.

Acetylcholinesterase (AChE) activity in the rat subfornical organ (SFO) was determined by the Koelle and Friedenwald method. Coronal sections showed a homogeneous reaction in the rostral region, which adopted a ring-like form in the anteromedial zone and a horseshoe pattern in the posteromedial zone. In the latter, AChE-specific positive neurons had been observed clearly in our sections. In sagittal sections the enzymatic reaction was intense in the anterior subependymal zone and dorsal region, and it continued caudally to the hippocampal area. The enzymatic activity was absent in the central region of the anteromedial zone and the subependymal region of the posteromedial zone. In sagittal sections the reaction was strongly positive in the periphery of the organ and negative in the posteromedial zone, near the choroid plexuses. Thus, we have shown that each region of the SFO presents a particular distribution of the AChE activity, related in some cases to neurons and in others to nerve fibers.

Acetylcholinesterase↗