A drug that is used to treat myasthenia gravis (a rare autoimmune disorder that causes muscle weakness). Neostigmine increases the activity of acetylcholine, a neurotransmitter that stimulates the contraction of muscles.
Possible adverse effects of neostigmine include nausea and vomiting, increased salivation, abdominal cramps, diarrhoea, blurred vision, muscle cramps, sweating, and twitching.
An ANTICHOLINESTERASE drug which enhances neuromuscular transmission – the passage of chemical messages between nerve and muscle cells – in voluntary and involuntary muscles in patients with the disorder MYASTHENIA GRAVIS. Its e?ect lasts for about four hours. A disadvantage is that it has a marked cholinergic action – affecting heart rhythm, causing excessive salivation and tear secretion, constricting the BRONCHIOLES and stimulating the gastrointestinal tract.
n. an *anticholinesterase drug used mainly to diagnose and treat *myasthenia gravis and to reverse the action of nondepolarizing *muscle-relaxant drugs used during surgery. Side-effects include abdominal cramps, diarrhoea, increased salivation, and a slow heart rate (*bradycardia).
Any compound that inhibits the activity of CHOLINESTERASE, thus permitting ACETYLCHOLINE to continue its function of transmitting nerve impulses. Drugs with anticholinesterase properties include distigmine, NEOSTIGMINE and PHYSOSTIGMINE.... anticholinesterase
These drugs produce partial or complete paralysis of skeletal muscle (see under MUSCLE – Structure of muscle). Drugs in clinical use are all reversible and are used to help insert a breathing tube into the TRACHEA (endotracheal tube) during general ANAESTHESIA and ARTIFICIAL VENTILATION OF THE LUNGS. They may be broadly divided into depolarising and nondepolarising muscle relaxants. Depolarising muscle relaxants act by binding to acetylcholine receptors at the motor end-plate where nerves are attached to muscle cells, and producing a more prolonged depolarisation than acetylcholine, which results in initial muscle fasciculation (overactivity) and then ?accid paralysis of the muscle. The only commonly used depolarising drug is succinylcholine which has a rapid onset of action and lasts approximately three minutes. Non-depolarising muscle relaxants bind to the acetylcholine receptors, preventing acetylcholine from gaining access to them. They have a slower onset time and longer duration than depolarisers, although this varies widely between di?erent drugs. They are competitive antagonists and they may be reversed by increasing the concentration of acetylcholine at the motor end-plate using an anticholinesterase agent such as neostigmine. These drugs are broken down in the liver and excreted through the kidney, and their action will be prolonged in liver and renal failure. Other uses include the relief of skeletal muscle spasms in TETANUS, PARKINSONISM and spastic disorders. The drugs dantrolene and diazepam are used in these circumstances.... muscle relaxants
n. an *antimuscarinic drug that occurs in deadly nightshade (see belladonna). Because it dilates the pupil and paralyses the ciliary muscle (see cycloplegia; mydriatic), atropine is used in eye examinations and the treatment of anterior *uveitis. It is also administered by injection to treat a slow heart rate (*bradycardia) associated with arrhythmias or, with *neostigmine, to reverse the action of muscle relaxants used during surgery. It is sometimes used to treat gut spasms and – rarely – for *premedication. Common side-effects include dryness of the throat, thirst, impaired vision, and increased heart rate.... atropine
(Ogilvie’s syndrome) n. functional impairment of intestinal peristalsis without evidence of an obstructing lesion (acute colonic pseudo-obstruction). It presents with vomiting, marked abdominal distension, and constipation. It commonly occurs in hospitalized patients with serious illness, probably caused by abnormalities in colonic autonomic regulation and often associated with trauma, sepsis, the postoperative state following abdominal, pelvic, or orthopaedic surgery, or cardiac dysfunction (heart failure, myocardial infarction). Management is usually conservative and involves treatment of the underlying condition, the ‘drip and suck’ approach (see ileus), decompression of the colon, and prokinetic agents (such as neostigmine). Surgery is required when the conservative approach fails or in cases of perforation.... pseudo-obstruction