Substance p: localization in the central nervous system and in some primary sensory neurons

Science ◽  
1975 ◽  
Vol 190 (4217) ◽  
pp. 889-890 ◽  
Author(s):  
T. Hokfelt ◽  
J. Kellerth ◽  
G. Nilsson ◽  
B. Pernow
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Substance P ◽  
Sensory Neurons ◽  
Primary Sensory Neurons ◽  
The Central Nervous System

Renorenal Reflexes: Role of Substance P and Prostaglandins

Physiology ◽  
1993 ◽  
Vol 8 (5) ◽  
pp. 228-232
Author(s):  
UC Kopp
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Substance P ◽  
Sensory Neurons ◽  
Urine Output ◽  
The Central Nervous System ◽  
Pelvic Pressure

The kidney is capable of transmitting information from sensory neurons to the central nervous system. Prostaglandins and substance P contribute to the activation of renal sensory neurons produced by increases in renal pelvic pressure that lead to a reflex increase in contralateral urine output.

Glucuronyl 3-sulfate occurs exclusively on distal unmyelinated terminals of selected sensory neurons in the peripheral nervous system

1995 ◽  
Vol 53 ◽  
pp. 958-959
Author(s):  
S.S. Spicer ◽  
B.A. Schulte
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Cerebral Cortex ◽  
Peripheral Nervous System ◽  
Sensory Neurons ◽  
Sensory Nerves ◽  
Tissue Antigens ◽  
The Central Nervous System ◽  
The Brain ◽  
Leu 7

Generation of monoclonal antibodies (MAbs) against tissue antigens has yielded several (VC1.1, HNK- 1, L2, 4F4 and anti-leu 7) which recognize the unique sugar epitope, glucuronyl 3-sulfate (Glc A3- SO4). In the central nervous system, these MAbs have demonstrated Glc A3-SO4 at the surface of neurons in the cerebral cortex, the cerebellum, the retina and other widespread regions of the brain.Here we describe the distribution of Glc A3-SO4 in the peripheral nervous system as determined by immunostaining with a MAb (VC 1.1) developed against antigen in the cat visual cortex. Outside the central nervous system, immunoreactivity was observed only in peripheral terminals of selected sensory nerves conducting transduction signals for touch, hearing, balance and taste. On the glassy membrane of the sinus hair in murine nasal skin, just deep to the ringwurt, VC 1.1 delineated an intensely stained, plaque-like area (Fig. 1). This previously unrecognized structure of the nasal vibrissae presumably serves as a tactile end organ and to our knowledge is not demonstrable by means other than its selective immunopositivity with VC1.1 and its appearance as a densely fibrillar area in H&E stained sections.

Molecular Biology of Vertebrate Olfactory Receptors and Circuits

2021 ◽  
Author(s):  
Richard P. Tucker ◽  
Qizhi Gong
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Olfactory Bulb ◽  
Gene Family ◽  
Sensory Neuron ◽  
Sensory Neurons ◽  
Odorant Receptor ◽  
Vomeronasal Organ ◽  
Odorant Receptors ◽  
The Central Nervous System

Animals use their olfactory system for the procurement of food, the detection of danger, and the identification of potential mates. In vertebrates, the olfactory sensory neuron has a single apical dendrite that is exposed to the environment and a single basal axon that projects to the central nervous system (i.e., the olfactory bulb). The first odorant receptors to be discovered belong to an enormous gene family encoding G protein-coupled seven transmembrane domain proteins. Odorant binding to these classical odorant receptors initiates a GTP-dependent signaling cascade that uses cAMP as a second messenger. Subsequently, additional types of odorant receptors using different signaling pathways have been identified. While most olfactory sensory neurons are found in the olfactory sensory neuroepithelium, others are found in specialized olfactory subsystems. In rodents, the vomeronasal organ contains neurons that recognize pheromones, the septal organ recognizes odorant and mechanical stimuli, and the neurons of the Grüneberg ganglion are sensitive to cool temperatures and certain volatile alarm signals. Within the olfactory sensory neuroepithelium, each sensory neuron expresses a single odorant receptor gene out of the large gene family; the axons of sensory neurons expressing the same odorant receptor typically converge onto a pair of glomeruli at the periphery of the olfactory bulb. This results in the transformation of olfactory information into a spatially organized odortopic map in the olfactory bulb. The axons originating from the vomeronasal organ project to the accessory olfactory bulb, whereas the axons from neurons in the Grüneberg ganglion project to 10 specific glomeruli found in the caudal part of the olfactory bulb. Within a glomerulus, the axons originating from olfactory sensory neurons synapse on the dendrites of olfactory bulb neurons, including mitral and tufted cells. Mitral cells and tufted cells in turn project directly to higher brain centers (e.g., the piriform cortex and olfactory tubercle). The integration of olfactory information in the olfactory cortices and elsewhere in the central nervous system informs and directs animal behavior.

Projections from sensory neurons developing at ectopic sites in insects

Development ◽  
1981 ◽  
Vol 65 (Supplement) ◽  
pp. 209-224
Author(s):  
Hilary Anderson
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Sensory Neurons ◽  
Sensory Systems ◽  
Genetic Mutation ◽  
Detailed Understanding ◽  
Giant Interneuron ◽  
The Central Nervous System ◽  
Ectopic Neurons

This paper reviews recent experiments which attempt to gain more understanding about the recognition processes involved in the formation of neuronal connexions by studying the degree of specificity with which sensory neurons form their central connexions. This is done by generating ectopic neurons (either by transplantation or by genetic mutation) whose axons grow into novel regions of the central nervous system, and then examining their projections and synapses. The sensory systems reviewed are: the Antennapedia, spineless-aristapedia, proboscipedia, and bithorax homeotic mutants of Drosphila melanogaster; the cercus-to-giant interneuron system of crickets, and the wind-sensitive hair system of locusts. The results show that ectopic neurons form projections that are discrete and characteristic, not random and chaotic. In those cases where single classes of sensilla have been studied, they follow either their normal CNS pathways or those pathways normally used by their segmental homologues. Ectopic sensory neurons can also form appropriate functional connexions in some cases but not in others. Possible reasons are discussed, but detailed understanding of the underlying events requires further experimentation.

Distribution and release of Substance P in the central nervous system

1978 ◽  
pp. 135-155 ◽  
Author(s):  
A. C. Cuello ◽  
P. Emson ◽  
M. del Fiacco ◽  
J. Gale ◽  
L. L. Iversen ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Substance P ◽  
The Central Nervous System

scholarly journals FURTHER OBSERVATION ON THE LACK OF ACTIVE UPTAKE SYSTEM FOR SUBSTANCE P IN THE CENTRAL NERVOUS SYSTEM

1977 ◽  
Vol 27 (4) ◽  
pp. 573-580 ◽  
Author(s):  
Tomio SEGAWA ◽  
Yoshihiro NAKATA ◽  
Haruaki YAJIMA ◽  
Kouki KITAGAWA
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Substance P ◽  
Uptake System ◽  
Active Uptake ◽  
The Central Nervous System

Leech Mechanosensation

2017 ◽  
Author(s):  
Brian D. Burrell
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Sensory Neurons ◽  
Receptive Fields ◽  
Model Systems ◽  
Sensory Cells ◽  
Mechanical Stimuli ◽  
Nociceptive Neurons ◽  
Mechanosensory Neurons ◽  
The Central Nervous System

The medicinal leech (Hirudo verbana) is an annelid (segmented worm) and one of the classic model systems in neuroscience. It has been used in research for over 50 years and was one of the first animals in which intracellular recordings of mechanosensory neurons were carried out. Remarkably, the leech has three main classes of mechanosensory neurons that exhibit many of the same properties found in vertebrates. The most sensitive of these neurons are the touch cells, which are rapidly adapting neurons that detect low-intensity mechanical stimuli. Next are the pressure cells, which are slow-adapting sensory neurons that respond to higher intensity, sustained mechanostimulation. Finally, there are nociceptive neurons, which have the highest threshold and respond to potentially damaging mechanostimuli, such as a pinch. As observed in mammals, the leech has separate mechanosensitive and polymodal nociceptors, the latter responding to mechanical, thermal, and chemical stimuli. The cell bodies for all three types of mechanosensitive neurons are found in the central nervous system where they are arranged as bilateral pairs. Each neuron extends processes to the skin where they form discrete receptive fields. In the touch and pressure cells, these receptive fields are arranged along the dorsal-ventral axis. For the mechano-only and polymodal nociceptive neurons, the peripheral receptive fields overlap with the mechano-only nociceptor, which also innervates the gut. The leech also has a type of mechanosensitive cell located in the periphery that responds to vibrations in the water and is used, in part, to detect potential prey nearby. In the central nervous system, the touch, pressure, and nociceptive cells all form synaptic connections with a variety of motor neurons, interneurons, and even each other, using glutamate as the neurotransmitter. Synaptic transmission by these cells can be modulated by a variety of activity-dependent processes as well as the influence of neuromodulatory transmitters, such as serotonin. The output of these sensory neurons can also be modulated by conduction block, a process in which action potentials fail to propagate to all the synaptic release sites, decreasing synaptic output. Activity in these sensory neurons leads to the initiation of a number of different motor behaviors involved in locomotion, such as swimming and crawling, as well as behaviors designed to recoil from aversive/noxious stimuli, such as local bending and shortening. In the case of local bending, the leech is able to bend in the appropriate direction away from the offending stimuli. It does so through a combination of which mechanosensory cell receptive fields have been activated and the relative activation of multiple sensory cells decoded by a layer of downstream interneurons.

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