Fate of B1–B2 and B3 rhombencephalic cells transplanted into the transected spinal cord of adult rats: Light and electron microscopic studies

1992 ◽  
Vol 117 (1) ◽  
pp. 59-70 ◽  
Author(s):  
N. Rajaofetra ◽  
N. König ◽  
P. Poulat ◽  
L. Marlier ◽  
F. Sandillon ◽  
...  
1996 ◽  
Vol 33 (3) ◽  
pp. 365-366 ◽  
Author(s):  
D. Y. Rim ◽  
D. Y. Cho ◽  
H. W. Taylor

Lysosomal storage disease involving the brain, spinal cord, liver, and spleen was discovered in a 6-month-old male emu ( Dromaius novaehollandiae). The diagnosis was based on light and electron microscopic studies and histochemical staining characteristics. This is the first case of lysosomal storage disease reported in a ratite.


Recent findings on the afferent and efferent connexions of the striatum (the caudate nucleus and putamen) and globus pallidus have been summarized in an orderly sequence. The striatum receives afferent fibres from three main sources, the cerebral cortex, the intralaminar nuclei of the thalamus and the midbrain; the major features of each of these pathways are outlined. The striatum sends efferent fibres to the globus pallidus and the substantia nigra, and the two segments of the globus pallidus in turn project upon the subthalamic nucleus and upon the thalamus and midbrain tegmentum. Through the thalamus the major influence of the striopallidum is upon the motor area of the cerebral cortex, and it is suggested that through the midbrain tegmentum there may also be a descending influence upon the spinal cord. These findings from light microscopical investigations are synthesized with observations made in electron microscopic studies of the striatum and globus pallidus. On the basis of present knowledge of their structure and connexions attention is drawn to several marked similarities between these parts of the basal ganglia and the cerebellum.


2000 ◽  
Vol 44 (2) ◽  
pp. 261-266 ◽  
Author(s):  
Mehdi Shakibaei ◽  
Kerstin Pfister ◽  
Rudolf Schwabe ◽  
Jürgen Vormann ◽  
Ralf Stahlmann

ABSTRACT Fluoroquinolones can cause tendinitis and tendon rupture. However, toxicological as well as clinical information on quinolone-induced tendopathy is scarce. We performed extensive electron microscopic studies with Achilles tendon specimens from ofloxacin-treated rats. The drug was given at a dose of 1,200 mg/kg (body weight) orally. Juvenile Wistar rats received one or three oral doses each of 1,200 mg of ofloxacin/kg (body weight)/day. Three days after treatment, the tenocytes of their Achilles tendons showed degenerative alterations, such as multiple vacuoles and vesicles in the cytoplasm that had developed due to swellings and dilatations of cell organelles. Other indications of cell degradation were the occurrence of cell debris and cell detachment from the extracellular matrix accompanied by a loss of cell-matrix interaction. The tenocytes of juvenile Wistar rats that had been treated at day 36 with a single oral dose of 1,200 mg of ofloxacin/kg (body weight) and sacrificed either 3 or 6 months later exhibited similar degenerative alterations. The number of degenerative alterations of tenocytes after ofloxacin treatment was considerably higher in rats that had received a magnesium-deficient diet than in rats with normal magnesium status. Of the adult rats that had been treated once, 5 times, and 10 times with ofloxacin and killed 1 day later, only those with the 10-times treatment showed a significantly increased number of degeneratively altered tenocytes. In summary, effects observed in tendons show similar pathological features as described earlier in cartilage, indicating that quinolone-induced arthropathy and quinolone-induced tendopathy probably are different clinical manifestations of the same toxic effect on cellular components of connective tissue structures.


1974 ◽  
Vol 22 (8) ◽  
pp. 802-811 ◽  
Author(s):  
ANITA A. SURAN

Histochemical procedures show a concentrated zone of phosphomonoesterase activity in the substantia gelatinosa of mouse spinal cord which represents at least two enzymic activities. At pH 7,5'-nucleotidase activity is observed in both somata and neuropil, while at pH 5 the reaction is evident only in somata. An acid phosphatase of unknown specificity is seen in somata only and exhibits optimal activity near pH 5. No comparable enzymic reactions are observed in cat spinal cord sections. Electron microscopic studies demonstrate separate cytologic distributions of the two enzymic activities in substantia gelatinosa. With nucleotides, the reaction is confined to boundaries of processes within the neuropil and to nuclei at pH 7. At pH 5 using an acid phosphatase substrate, β-glycerol phosphate, slight reactions were noted within nerve fibers. Use of β-glycerol phosphate near pH 7 demonstrates both types of activity simultaneously, the boundary reactions typical of the nucleotidase and the reactions within axons and dendrites characteristic of the phosphatase.


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