The Pharmacology of Experimental Myopathies

التفاصيل البيبلوغرافية
العنوان: The Pharmacology of Experimental Myopathies
المؤلفون: Dettbarn Wd, Laskowski Mb
المصدر: Annual Review of Pharmacology and Toxicology. 17:387-409
بيانات النشر: Annual Reviews, 1977.
سنة النشر: 1977
مصطلحات موضوعية: Biogenic Amines, Serotonin, Time Factors, Toxicology, Bioinformatics, Nervous System, Muscular Dystrophies, Membrane Potentials, Myotonia, Muscular Diseases, Human muscle, Animals, Cholinesterases, Humans, Medicine, Myopathy, Ligation, Pharmacology, Neurotransmitter Agents, business.industry, Goats, Muscles, Dystrophy, Muscle weakness, Neuromuscular Diseases, medicine.disease, Rats, Enzyme Activation, Disease Models, Animal, Cholesterol, Muscle disease, Neurologic abnormalities, Cholinesterase Inhibitors, 2,4-Dichlorophenoxyacetic Acid, Anura, medicine.symptom, business, Large group
الوصف: A large group of disorders affect striated muscle in man. The direct approach to the study of these diseases presents major difficulties. Biopsies can be useful in diagnos­ ing a muscle disease and in confirming its progress. However, at a time when muscle weakness and other neurologic abnormalities become obvious, the myopathy is usually well advanced. It is also impossible to provide adequate controls to follow the development of the myopathy in man and its reversibility with experimental techniques. Consequently, a wide variety of animal models of human muscle dis­ eases have been developed. These models include myopathies occurring spontane­ ously in highly inbred strains of mice, hamsters, goats, and other mammals. However, a new and rapidly expanding area of inquiry involves the pharmacologi­ cally induced myopathies developed with a wide variety of drugs. This review is concerned with this second area of research, that of pharmacologically induced experimental myopathies. A survey of the literature of the past ten years reveals many attempts to reproduce pharmacologically human myopathies in animals. Three areas have been particu­ larly active. These include experimental myotonia, experimental Duchenne's mus­ cular dystrophy, and general neuromuscular disorders.
تدمد: 1545-4304
0362-1642
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c68a20f188a6ec008637342d4e1b48eTest
https://doi.org/10.1146/annurev.pa.17.040177.002131Test
رقم الانضمام: edsair.doi.dedup.....4c68a20f188a6ec008637342d4e1b48e
قاعدة البيانات: OpenAIRE