scholarly journals STUDIES ON PSEUDORABIES (INFECTIOUS BULBAR PARALYSIS, MAD ITCH)

1934 ◽  
Vol 59 (6) ◽  
pp. 729-749 ◽  
Author(s):  
E. Weston Hurst

After intramuscular, intradermal and subcutaneous inoculation, the pseudorabies virus reaches the central nervous system by way of the peripheral nerves, although it is circulating in the blood. Centrifugal spread from the infected nervous tissues by the neural route also occurs. After intracerebral inoculation the virus passes in the reverse direction, down the nervous axis. The Aujeszky strain invades the blood stream more readily than does the Iowa strain; but possibly with repeated passage the latter is approximating in this respect more closely the classical Aujeszky strain. After intravenous inoculation, effective with even small doses, virus is rapidly removed from the blood, and multiple infective foci are established in various organs; thence ascent of the virus by the peripheral nerves leads to infection of the central nervous system, the symptomatology differing according to whether the spinal cord or the medulla is first reached. The lack of evidence that the virus can penetrate directly the hemato-encephalic barrier deserves emphasis. When subcutaneous inoculation is practised in an area deprived of its nerve supply, the ability of the virus to invade the blood stream permits it to establish infective foci in the various viscera, and, after a predictable delay, the course of infection resembles that following intravenous injection. The pseudorabies virus is pantropic; i.e., it readily attacks cells derived from any embryonic layer. Lesions in the adrenal gland following intravenous inoculation are very like those due to herpes virus similarly introduced, this being one point of similarity in the pathogenic action of the two organisms. The relation of the pseudorabies virus to other viruses affecting the central nervous system is discussed.

Cell ◽  
1994 ◽  
Vol 76 (1) ◽  
pp. 117-129 ◽  
Author(s):  
David Westaway ◽  
Stephen J. DeArmond ◽  
Juliana Cayetano-Canlas ◽  
Darlene Groth ◽  
Dallas Foster ◽  
...  

1981 ◽  
Vol 88 (1) ◽  
pp. 67-72 ◽  
Author(s):  
P F Davison ◽  
R N Jones

Several classes of 10-nm filaments have been reported in mammalian cells and they can be distinguished by the size of their protein subunit. We have studied the distribution of these filaments in nerves from calves and other mammals. From the display on polyacrylamide electrophoretic gels of proteins in extracts from fibroblast and central, cranial and peripheral nerves, we cut the appropriate stained bands and prepared iodinated peptide maps. The similarities between the respective maps provide strong evidence for the presence of vimentin in cranial and peripheral nerves. The glial fibrillary acidic protein was found in axon preparations from the central nervous system, but was not identified in distal segments of some cranial nerves, nor in peripheral nerve.


2008 ◽  
Vol 173 (6) ◽  
pp. 1669-1681 ◽  
Author(s):  
Sonja Hochmeister ◽  
Manuel Zeitelhofer ◽  
Jan Bauer ◽  
Eva-Maria Nicolussi ◽  
Marie-Therese Fischer ◽  
...  

1994 ◽  
Vol 107 (2) ◽  
pp. 543-552 ◽  
Author(s):  
C.M. Niessen ◽  
O. Cremona ◽  
H. Daams ◽  
S. Ferraresi ◽  
A. Sonnenberg ◽  
...  

Integrin alpha 6 beta 4 is expressed in human peripheral nerves, but not in the central nervous system. This integrin heterodimer has previously been found in perineural fibroblast-like cells and in Schwann cells (SCs), which both assemble a basement membrane but do not form hemidesmosomes. We show here that in SCs, which had formed a myelin sheath, alpha 6 beta 4 was enriched in the proximity of the nucleus, at Ranvier paranodal areas and at Schmitt-Lanterman clefts; alpha 6 beta 4 was also found at the grooved interface between small axons and non-myelinating SCs. Immunoprecipitation of human peripheral nerves, in combination with Western blotting showed that beta 4 is associated with the alpha 6A subunit. Northern blot analysis of human peripheral nerves showed a single beta 4 transcript of 6 kb. Using the reverse transcriptase polymerase chain reaction, we detected two mRNA species, one for the most common (−70, -53) form of beta 4 and the other encoding the (+53) variant of beta 4. Cultured SCs were devoid of alpha 6 beta 4 but expressed alpha 6 beta 1, indicating that SCs lose beta 4 expression when contact with neurons is lost. Thus, resting SCs in contact with axons express alpha 6A in combination with beta 4, irrespective of myelin formation. We suggest that alpha 6 beta 4 expressed in SCs plays a role in peripheral neurogenesis.


1926 ◽  
Vol 22 (5-6) ◽  
pp. 748-749
Author(s):  
G. Pervushin

Prof. VV Korelin (Psycho-Neur. Jur., 1926, issue I), having applied this treatment at 23 patients, observed full recovery in 8 cases, syphilis of the central nervous system, at combined treatment with mercury, - 4 sl., Inflammation of peripheral nerves - 3 sl. And epidemic meningitis - 1 sl.); further, in 3 cases this treatment gave improvement, and in others remained without result.


2009 ◽  
Vol 296 (3) ◽  
pp. R501-R511 ◽  
Author(s):  
C. Kay Song ◽  
Gary J. Schwartz ◽  
Timothy J. Bartness

The origins of the sympathetic nervous system (SNS) innervation of white adipose tissue (WAT) have been defined using the transneuronal viral retrograde tract tracer, pseudorabies virus. Activation of this SNS innervation is acknowledged as the principal initiator of WAT lipolysis. The central control of WAT lipolysis may require neural feedback to a brain-SNS-WAT circuit via WAT afferents. Indeed, conventional tract tracing studies have demonstrated that peripheral pseudounipolar dorsal root ganglion (DRG) sensory cells innervate WAT. The central nervous system projections of WAT afferents remain uncharted, however, and form the focus of the present study. We used the H129 strain of the herpes simplex virus-1 (HSV-1), an anterograde transneuronal viral tract tracer, to define the afferent circuits projecting from WAT to the central nervous system. Siberian hamster inguinal (IWAT) or epididymal WAT was injected with H129 and the neuraxis processed for HSV-1 immunoreactivity. We found substantial overlap in the pattern of WAT sensory afferent projections with multiple SNS outflow sites along the neuraxis, suggesting the possibility of WAT sensory-SNS circuits that could regulate WAT SNS drive and thereby lipolysis. Previously, we demonstrated that systemic 2-deoxy-d-glucose (2DG) elicited increases in the SNS drive to IWAT. Here, we show that systemic 2DG administration also significantly increases multiunit spike activity arising from decentralized IWAT afferents. Collectively, these data provide structural and functional support for the existence of a sensory WAT pathway to the brain, important in the negative feedback control of lipid mobilization.


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