Neuronal organization of the lateral basilar region of the cat spinal cord

The neuronal organization of the lateral basilar region (LBR) of gray matter in the cervical portion of the cat spinal cord was studied by light and electron microscopy. It was found that LBR neurons form a homogeneous group with regard to the size of their soma. The ordinary pale ultrastructure of the cytoplasm is found in 96.8% of neurons examined. The ultrastructure of the cytoplasm of the small cells (3.2%) is dark and their matrix has high electron density. Most endings on LBR neurons have spherical vesicles (of the S-type). Endings with flattened vesicles (F-type) are next in order of numerical frequency. In some endings, besides the ordinary synaptic vesicles, there are other vesicles with an osmiophilic center, and endings with a dense matrix and numerous spherical vesicles. Endings of the F-type are relatively more numerous on dendrites of LBR neurons than on their soma. Axodendritic synapses form 87.8% of the synaptic connections of the LBR, and axo-somatic synapses 9.2%. The few axo-axonal synapses are formed by small endings with small synaptic vesicles and large plaques with spherical vesicles. The latter frequently make contact with several dendrites simultaneously. The functional role of the various neuronal structures of LBR in the transmission of descending and afferent influences is discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. A. N. Severtsov Institute of Evolutionary Morphology and Ecology of Animals, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 4, No. 3, pp. 296–302, May–June, 1972.     

Propriospinal neurones as a relay system for transmission of cortico-spinal influences.

1. Synaptic organization and transmission have been studied in the lateral group of short propriospinal neurones of the lumbar and cervical regions of the cat spinal cord. Special attention was paid to their role in the transmission of cortico-spinal volleys. 2. The majority of these neurones are mono- or oligosynaptically excited after pyramidal tract stimulation. Convergence of excitatory actions from rubrospinal and lateral reticulospinal tracts was typical for these cells. Neurones with relatively low-level and delayed effects from segmental afferents are frequent in this population. 3. Temporal summation is important for the transmission of descending vlleys through these neurones. Mutual excitatory and recurrent inhibitory connections are supposed to play a substantial role in their function. 4. Possible participation of the short lateral propriospinal system in the transmission, transformation and re-distribution of corticofugal signals to the segmental spinal mechanisms is discussed.     

Activity of lumbar interneurons during late long-lasting discharges in motor nerves of immobilized thalamic cats

Activity of lumbar spinal neurons was recorded extracellularly during late long-lasting discharges in efferent nerves in immobilized thalamic cats. Of the total number of cells tested, 70% changed their activity during late discharges. The activity of 35% of neurons was increased during late discharges in nerves to flexors, but inhibited during discharges in nerves to extensors. Responses of 27% of neurons were of the opposite character. Other neurons were found whose activity was increased (5%) and reduced (3%), respectively, during later discharges in both flexor and extensor nerves. Most interneurons which changed their activity during late discharges were located in lateral parts of the intermediate zone of gray matter and the ventral horn at a depth of 2.8 mm. The character of the afferent input to a neuron was found to depend on the late efferent discharges and activity of the neurons correlated with them. Neurons whose activity was unchanged during late discharges (30%) were mainly located rather more dorsally, at a depth of about 2.0 mm. The possible mechanisms of the participation of these groups of interneurons in the generation of late discharges are discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 11, No. 3, pp. 236–244, May–June, 1979.     

Involvement of the Endoplasmic Reticulum of Chromaffin Cells of the Rat Adrenal Gland in Calcium Signaling

We studied the involvement of the endoplasmic reticulum (ER) in calcium signaling in rat chromaffin cells. For this purpose, the following agents influencing the activity of the ER were used: (i) Caffeine that activates the release of Ca²⁺ from the endoplasmic store and (ii) thapsigargin that suppresses accumulation of calcium in the ER. The intracellular Ca²⁺ concentration was measured with the help of a calcium-sensitive dye, Fura-2AM, using the microfluorescent technique. Applications of caffeine led to a rise in the level of free Ca²⁺ in the cell cytosol and also to a decrease in the amplitude of calcium transients induced by depolarization of the plasma membrane under the action of a hyperpotassium solution. Under conditions of repeated caffeine applications, the amplitude of transients decreased to 9% of its initial value, which is explained by exhaustion of the calcium stores. The action of caffeine was restored when the calcium stores were re-filled under the action of depolarization of the plasma membrane. Thapsigargin completely removed the effect of caffeine and did not influence KCl-induced transients. Therefore, our experiments are indicative of a significant importance of the ER calcium stores for calcium signaling in chromaffin cells, which allows us to hypothesize that these stores play an important role in the control of secretion of catecholamines.     

Glutathione peroxidase activity in the blood cells of psoriatic patients correlates with their responsiveness to Efalizumab

Biological treatment of psoriasis, a chronic inflammatory immune-mediated pathology of huge social impact, has become a recent revolutionizing breakthrough in the management of the disease. Apart from anti-TNF-alpha biologics, recombinant proteins-inhibitors of the T lymphocytes-antigen presenting cells interaction, Efalizumab among them, have been successfully used in the therapy of psoriasis. Serious concern regarding safety and efficacy of biologics remains because they induce numerous adverse effects and a significant number of patients are non-responders. Up-to-now, there are no biochemical or/and immunological markers of the clinical efficacy of these drugs. This study searches for immunological and redox markers of the clinical response in the group of psoriatic patients treated with Efalizumab. Clinical response to Efalizumab was assessed by Psoriasis Area and Severity Index and correlated with suppression of T-cell functions, plasma cytokines, membrane-associated polyunsaturated fatty acids (PUFAs), antioxidant enzymes and markers of oxidative stress. A 12-week Efalizumab therapy did not affect abnormal plasma levels of pro-inflammatory cytokines and lower-than-normal content of PUFAs esterified in phospholipids of red cell membranes. It did, however, suppress T-cell-mediated functions and decrease nitrites/nitrates and malonyl dialdehyde levels independently on the clinical outcome. On contrast, activities of glutathione peroxidase (GPx) and glutathione S-transferase in granulocytes were remarkably increased and catalase decreased exclusively in non-responders vs complete or partial responders. High baseline GPx in erythrocytes decreased in responders. It is concluded that clinical response to Efalizumab correlates with GPx activity in the blood cells, suggesting that high hydroperoxide levels are involved in psoriasis persistence.     

Streptozotocin-Induced Diabetes Mellitus and Further Nimodipine Treatment Do Not Change Calcium Currents in Rat Sensory Neurons within Early Stages of the Disease

Earlier, considerable prolongation of the depolarization-induced Ca²⁺ transients was demonstrated in primary sensory neurons of rats with streptozotocin (STZ)-induced diabetes mellitus. To analyze the nature of this effect, we examine possible changes in the characteristics of voltage-operated calcium channels. Neither the amplitude of Ca²⁺ currents provided by both high- and low-voltage activated calcium channels nor the respective current densities significantly changed within the early stages of diabetes mellitus. In rats treated with nimodipine, also no significant changes in the calcium channel activity were observed. Only in the case of a decrease in the external calcium concentration was some drop in the Ca²⁺ current amplitude observed. We conclude that within the early stages of diabetes mellitus there are no significant modifications in the structure of the membrane of primary sensory neurons manifested in the expression of Ca²⁺ channels, which might be responsible for the observed rapidly occurring changes in calcium signalling, cytosolic Ca²⁺ accumulation, and synaptic plasticity.     

Thiol antioxidants increase the intracellular level of reactive oxygen species and prolifetaion of SP2/0 mouse myeloma cells in serum-free medium

The connections between the presence of low molecular weight RSH-antioxidants (N-acetylcysteine, glutathione) in serum-free medium, generation of reactive oxygen species (ROS), and proliferation of SP2/0-SF mouse myeloma cells have been demonstrated. It is shown that the presence of RSH compounds in the medium within the studied range of concentrations changed the contents of ROS in cells and had a dose-dependent effect on cell proliferation. Stimulation of the proliferative activity did not depend on the nature of an RSH compound. The optimal concentration for the both antioxidants was 0.2 mM. A further increase of the concentration led to inhibition of cell proliferation to different degrees for N-acetylcysteine and glutathione.