decamethonium वाक्य
उदाहरण वाक्य
मोबाइल
- Decamethonium is sometimes, but rarely, used in clinical practice.
- Such as for decamethonium the straight line conformer is clearly the lowest energy state.
- Also, tubocurarine effects were known to be reversible by acetylcholinesterase inhibitors, whereas decamethonium and suxamethonium block were not reversible.
- Following research with decamethonium, scientists developed suxamethonium, which is a double acetylcholine molecule that was connected at the acetyl end.
- Decamethonium, which has a short action time, is similar to acetylcholine and acts as a partial agonist of the nicotinic acetylcholine receptor.
- Decamethonium does not produce unconsciousness or anesthesia, and its effects may cause considerable psychological distress while simultaneously making it impossible for a patient to communicate.
- Ironically, laudexium itself was invented by a cross-combination between the prototypical non-depolarizing agent, d-tubocurarine and the depolarizing agent, decamethonium.
- Taking additional observations into account, these researchers concluded that the effects on frog tissue of candicine most closely resembled those of the well-known depolarizing neuromuscular-blocking drug decamethonium.
- "' Decamethonium "'( "'Syncurine "') is a depolarizing muscle relaxant or neuromuscular blocking agent, and is used in anesthesia to induce paralysis.
- In the process of binding, decamethonium actually activates ( depolarizes ) the motor endplate-but since the decamethonium itself is not degraded, the membrane remains depolarized and unresponsive to normal acetylcholine release.
- In the process of binding, decamethonium actually activates ( depolarizes ) the motor endplate-but since the decamethonium itself is not degraded, the membrane remains depolarized and unresponsive to normal acetylcholine release.
- One of the outstanding recent contributions to pharmacology and therapeutics is his discovery, with Zaimis, of the actions of the methonium compounds-decamethonium a potent neuromuscular, and hexamethonium a potent ganglion blocking substance.
- In the 1950s and 1960s, the present-day concept of a neuromuscular blocking agent with a rapid onset and an ultra-short duration of action had not taken root : researchers and clinicians were still on the quest for potent but non-depolarizing replacements devoid of the histamine release and the dreaded " recurarizing " effects seen with tubocurarine and, more importantly, the absence of a depolarizing mechanism of action as seen with succinylcholine and decamethonium.
- From the 1950s through to the 1970s, the present-day concept of a neuromuscular blocking agent with a rapid onset and an ultra-short duration of action had not taken root : researchers and clinicians were still on the quest for potent but non-depolarizing replacements devoid of the histamine release and the dreaded " recurarizing " effects seen with tubocurarine and, more importantly, the absence of a depolarizing mechanism of action as seen with succinylcholine and decamethonium.
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