ANTICHOLINERGIC POISONING: TREATMENT WITH PHYSOSTIGMINE

PEDIATRICS ◽  
1973 ◽  
Vol 52 (3) ◽  
pp. 449-451
Author(s):  
Barry H. Rumack

The increased incidence of poisoning by overdoses of commonly used drugs with anticholinergic properties (Table I) and the general lack of knowledge concerning a specific treatment for these poisons warrants a summary of the problem at this time. Some plants containing anticholinergic alkaloids are also included in this group as they may also be taken intentionally or accidentally. Drugs with anticholinergic properties primanly antagonize acetylcholine competitively at the neuroreceptor site. Cardiac muscle, exocrine glands, and smooth muscle are most markedly affected.1 Action of the inhibitors is overcome by increasing the level of acetylcholine naturally generated in the body through inhibiting the enzyme (choline esterase) which normally prevents accumulation of excess acetylcholine. It does this by hydrolyzing that compound to inactive acetic acid and choline. Agents which inhibit this enzyme, so that acetylcholine accumulates at the neuroreceptor sites, are called anticholine esterases. Physostigmine, one of the anticholine esterases which is a tertiary amine, crosses into the central nervous system and can reverse both central and peripheral anticholinergic actions2. Neostigmine and pyridostigmine are also anticholine esterases but they are quaternary amines and are capable of acting only outside the central nervous system because of solubility and ionization characteristics. The anticholinergic syndrome has both central and peripheral signs and symptoms. Central toxic effects include anxiety, delirium, disorientation, hallucinations, hyperactivity, and seizures.2 Severe poisoning may produce coma, medullary paralysis, and death. Peripheral taxicity is characterized by tachycardia, hyperpyrexia, mydriasis, vasodilatation, urinary retention, diminution of gastrointestinal motility, decrease of secretion in salivary and sweat glands, and loss of secretions in the pharynx, bronchi, and nasal passages.

2016 ◽  
pp. 31-34
Author(s):  
Terrence D. Lagerlund

The variety of clinical neurophysiological studies corresponds to a variety of structural generators in the body, including muscles, sweat glands, peripheral nerves, and various components of the central nervous system. Each structural generator may have associated with it several different types of physiological potential. This chapter reviews the generators of electrophysiological potentials in terms of basic cellular electrophysiology and the anatomical structures that generate electrophysiological potentials of clinical interest. Knowledge of the generators of the potentials recorded in clinical neurophysiological studies is helpful in understanding the characteristics and distribution of the recorded potentials and is the first step in correlating the alterations seen in disease states with the pathological changes demonstrated in the underlying generators.


Author(s):  
F. L. Azizova ◽  
U. A. Boltaboev

The features of production factors established at the main workplaces of shoe production are considered. The materials on the results of the study of the functional state of the central nervous system of women workers of shoe production in the dynamics of the working day are presented. The level of functional state of the central nervous system was determined by the speed of visual and auditory-motor reactions, installed using the universal device chronoreflexometer. It was revealed that in the body of workers of shoe production there is an early development of inhibitory processes in the central nervous system, which is expressed in an increase in the number of errors when performing tasks on proofreading tables. It was found that the most pronounced shift s in auditory-motor responses were observed in professional groups, where higher levels of noise were registered in the workplace. The correlation analysis showed a close direct relationship between the growth of mistakes made in the market and the decrease in production. An increase in the time spent on the task indicates the occurrence and growth of production fatigue.Funding. The study had no funding.Conflict of interests. The authors declare no conflict of interests.


Author(s):  
Prithiv K R Kumar

Stem cells have the capacity to differentiate into any type of cell or organ. Stems cell originate from any part of the body, including the brain. Brain cells or rather neural stem cells have the capacitive advantage of differentiating into the central nervous system leading to the formation of neurons and glial cells. Neural stem cells should have a source by editing DNA, or by mixings chemical enzymes of iPSCs. By this method, a limitless number of neuron stem cells can be obtained. Increase in supply of NSCs help in repairing glial cells which in-turn heal the central nervous system. Generally, brain injuries cause motor and sensory deficits leading to stroke. With all trials from novel therapeutic methods to enhanced rehabilitation time, the economy and quality of life is suppressed. Only PSCs have proven effective for grafting cells into NSCs. Neurons derived from stem cells is the only challenge that limits in-vitro usage in the near future.


In the study of the phenomena of anaphylaxis there are certain points on which some measure of agreement seems to have been attained. In the case of anaphylaxis to soluble proteins, with which alone we are directly concerned in this paper, the majority of investigators probably accept the view that the condition is due to the formation of an antibody of the precipitin type. Concerning the method, however, by which the presence of this antibody causes the specific sensitiveness, the means by which its interaction with the antibody produces the anaphylactic shock, there is a wide divergence of conception. Two main currents of speculation can be discerned. One view, historically rather the earlier, and first put forward by Besredka (1) attributes the anaphylactic condition to the location of the antibody in the body cells. There is not complete unanimity among adherents of this view as to the nature of the antibody concerned, or as to the class of cells containing it which are primarily affected in the anaphylactic shock. Besredka (2) himself has apparently not accepted the identification of the anaphylactic antibody with a precipitin, but regards it as belonging to a special class (sensibilisine). He also regards the cells of the central nervous system as those primarily involved in the anaphylactic shock in the guinea-pig. Others, including one of us (3), have found no adequate reason for rejecting the strong evidence in favour of the precipitin nature of the anaphylactic antibody, produced by Doerr and Russ (4), Weil (5), and others, and have accepted and confirmed the description of the rapid anaphylactic death in the guinea-pig as due to a direct stimulation of the plain-muscle fibres surrounding the bronchioles, causing valve-like obstruction of the lumen, and leading to asphyxia, with the characteristic fixed distension of the lungs, as first described by Auer and Lewis (6), and almost simultaneously by Biedl and Kraus (7). But the fundamental conception of anaphylaxis as due to cellular location of an antibody, and of the reaction as due to the union of antigen and antibody taking place in the protoplasm, is common to a number of workers who thus differ on details.


1957 ◽  
Vol 34 (3) ◽  
pp. 306-333
Author(s):  
G. M. HUGHES

I. The effects of limb amputation and the cutting of commissures on the movements of the cockroach Blatta orientalis have been investigated with the aid of cinematography. Detailed analyses of changes in posture and rhythm of leg movements are given. 2. It is shown that quite marked changes occur following the amputation of a single leg or the cutting of a single commissure between the thoracic ganglia. 3. Changes following the amputation of a single leg are immediate and are such that the support normally provided by the missing leg is taken over by the two remaining legs on that side. Compensatory movements are also found in the contralateral legs. 4. When two legs of opposite sides are amputated it has been confirmed that the diagonal sequence tends to be adopted, but this is not invariably true. Besides alterations in the rhythm which this may involve, there are again adaptive modifications in the movements of the limbs with respect to the body. 5. When both comrnissures between the meso- and metathoracic ganglia are cut, the hind pair of legs fall out of rhythm with the other four legs. The observations on the effects of cutting commissures stress the importance of intersegmental pathways in co-ordination. 6. It is shown that all modifications following the amputation of legs may be related to the altered mechanical conditions. Some of the important factors involved in normal co-ordination are discussed, and it is suggested that the altered movements would be produced by the operation of these factors under the new conditions. It is concluded that the sensory inflow to the central nervous system is of major importance in the co-ordination of normal movement.


1981 ◽  
Vol 96 (3) ◽  
pp. 394-397 ◽  
Author(s):  
Jau-Nan Lee ◽  
Markku Seppälä ◽  
Tim Chard

Abstract. High pressure liquid chromatography (HPLC) and radioimmunoassay were employed to characterize luteinizing hormone-releasing factor (LRF)-like material in the human placenta. Methanol extracts of the placenta were washed with acetic acid and chloroform, further purified on coarse octadecylsilane columns, fractionated on HPLC, and tested by radioimmunoassay. In HPLC, placental LRF had the same retention time as synthetic LRF, and such fractions gave an inhibition curve which was parallel to that of synthetic LRF in radioimmunoassav. It is concluded that human placental I.RF is similar or identical to LRF in the central nervous system.


1998 ◽  
Vol 84 (3) ◽  
pp. 408-411 ◽  
Author(s):  
Maria Laura Del Basso De Caro ◽  
Antonella Siciliano ◽  
Paolo Cappabianca ◽  
Alessandra Alfieri ◽  
Enrico de Divitiis

Paragangliomas are usually benign tumors which can be found in many sites of the body, from the base of the skull down to the pelvic floor. In the central nervous system the sellar region is very rarely involved; only three well studied cases have been reported to date. We present the cytological, histological, histochemical, immunocytochemical and ultrastructural features of an intrasellar and suprasellar paraganglioma in an 84-year-old man.


2015 ◽  
Vol 309 (10) ◽  
pp. C660-C668 ◽  
Author(s):  
Victoria L. Hodgkinson ◽  
Sha Zhu ◽  
Yanfang Wang ◽  
Erik Ladomersky ◽  
Karen Nickelson ◽  
...  

Menkes disease is a fatal neurodegenerative disorder arising from a systemic copper deficiency caused by loss-of-function mutations in a ubiquitously expressed copper transporter, ATP7A. Although this disorder reveals an essential role for copper in the developing human nervous system, the role of ATP7A in the pathogenesis of signs and symptoms in affected patients, including severe mental retardation, ataxia, and excitotoxic seizures, remains unknown. To directly examine the role of ATP7A within the central nervous system, we generated Atp7a Nes mice, in which the Atp7a gene was specifically deleted within neural and glial cell precursors without impairing systemic copper homeostasis, and compared these mice with the mottled brindle ( mo-br) mutant, a murine model of Menkes disease in which Atp7a is defective in all cells. Whereas mo-br mice displayed neurodegeneration, demyelination, and 100% mortality prior to weaning, the Atp7a Nes mice showed none of these phenotypes, exhibiting only mild sensorimotor deficits, increased anxiety, and susceptibility to NMDA-induced seizure. Our results indicate that the pathophysiology of severe neurological signs and symptoms in Menkes disease is the result of copper deficiency within the central nervous system secondary to impaired systemic copper homeostasis and does not arise from an intrinsic lack of ATP7A within the developing brain. Furthermore, the sensorimotor deficits, hypophagia, anxiety, and sensitivity to NMDA-induced seizure in the Atp7a Nes mice reveal unique autonomous requirements for ATP7A in the nervous system. Taken together, these data reveal essential roles for copper acquisition in the central nervous system in early development and suggest novel therapeutic approaches in affected patients.


1948 ◽  
Vol s3-89 (5) ◽  
pp. 1-45
Author(s):  
J.A. C. NICOL

1. A description is given of the main features of the central nervous system of Myxicola infundibulum Rénier. 2. The nerve-cord is double in the first four thoracic segments and single posteriorly. It shows segmental swellings but is not ganglionated in the usual sense in that nerve-cell accumulations are not related directly to such swellings of the cord. 3. A very large axon lies within the dorsal portion of the nerve-cord and extends from the supra-oesophageal ganglia to the posterior end of the animal. It is small in the head ganglia where it passes transversely across the mid-line, increases in diameter in the oesophageal connectives, and expands to very large size, up to 1 mm., in the posterior thorax and anterior abdomen, and gradually tapers off to about 100µ in the posterior body. It shows segmental swellings corresponding to those of the nerve-cord in each segment. It occupies about 27 per cent, of the volume of the central nervous system and 0.3 per cent, of the volume of the animal. The diameter of the fibre increases during contraction of the worm. 4. The giant fibre is a continuous structure throughout its length, without internal dividing membranes or septa. Usually a branch of the giant fibre lies in each half of the nerve-cord in the anterior thoracic segments and these several branches are continuous with one another longitudinally and transversely. 5. The giant fibre is connected with nerve-cells along its entire course; it arises from a pair of cells in the supra-oesophageal ganglia, and receives the processes of many nerve-cells in each segment. There is no difference between the nerve-cells of the giant fibre and the other nerve-cells of the cord. 6. A distinct fibrous sheath invests the giant fibre. A slight concentration of lipoid can be revealed in this sheath by the use of Sudan black. 7. About eight peripheral branches arise from the giant fibre in each segment. They have a complex course in the nerve-cord where they anastomose with one another and receive the processes of nerve-cells. Peripherally, they are distributed to the longitudinal musculature. 8. Specimens surviving 16 days following section of the nerve-cord in the thorax have shown that the giant fibre does not degenerate in front of or behind a cut, thus confirming that it is a multicellular structure connected to nerve-cells in the thorax and abdomen. 9. It is concluded that the giant fibre of M. infundibulum is a large syncytial structure, extending throughout the entire central nervous system and the body-wall of the animal. 10. The giant fibre system of M. aesthetica resembles that of M. infundibulum. 11. Some implications of the possession of such a giant axon are discussed. It is suggested that its size, structure, and simplicity lead to rapid conduction and thus effect a considerable saving of reaction time, of considerable value to the species when considered in the light of the quick contraction which it mediates. The adoption of a sedentary mode of existence has permitted this portion of the central nervous system to become developed at the expense of other elements concerned with errant habits.


Bioprinting ◽  
2021 ◽  
pp. 98-118
Author(s):  
Kenneth Douglas

Abstract: This chapter recounts bioprinting studies of skin, bone, skeletal muscle, and neuromuscular junctions. The chapter begins with a study of bioprinted skin designed to enable the creation of skin with a uniform pigmentation. The chapter relates two very different approaches to bioprinted bone: a synthetic bone called hyperelastic bone and a strategy that prints cartilage precursors to bone and then induces the conversion of the cartilage to bone by judicious choice of bioinks. Muscles move bone, and the chapter discusses an investigation of bioprinted skeletal muscle. Finally, the chapter considers an attempt to bioprint a neuromuscular junction, a synapse—a minute gap—of about 20 billionths of a meter between a motor neuron and the cell membrane of a skeletal muscle cell. A motor neuron is a nerve in the central nervous system that sends signals to the muscles of the body.


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