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  • 匿名
关注:1 2013-05-23 12:21

求翻译:通常,阿托品作为麻醉前用药减少腺体分泌,但是阿托品是非选择性M受体阻滞药,使用后增加心率,增加心肌耗氧,而长托宁选择性作用于M1,M3受体,对M2受体几乎没有作用,不增加心脏氧耗,可以比较安全用于老年患者和心肌缺血患者。是什么意思?

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通常,阿托品作为麻醉前用药减少腺体分泌,但是阿托品是非选择性M受体阻滞药,使用后增加心率,增加心肌耗氧,而长托宁选择性作用于M1,M3受体,对M2受体几乎没有作用,不增加心脏氧耗,可以比较安全用于老年患者和心肌缺血患者。
问题补充:

  • 匿名
2013-05-23 12:21:38
Generally, atropine as a pre-anesthetic medication to reduce the glandular secretion, but the atropine non-selective m receptor blockers, the use of increased heart rate, increased myocardial oxygen consumption, and Changtuoning selective role in the m1, m3 receptor, m2 receptor almost no effect, no
  • 匿名
2013-05-23 12:23:18
Typically, atropine as a pre-anesthesia medications reduce glandular secretions, but non-selective atropine M-block products after use, increase heart rate, increased myocardial oxygen consumption, and long and rather selective role in M M 1, 3, 2 of the Commonwealth M almost no role, not to increas
  • 匿名
2013-05-23 12:24:58
Usually, the atropine took before the anaesthesia applies drugs the reduced gland secretion, but the atropine right and wrong selective M acceptor hinders the medicine, after the use to increase the heart rate, the increase cardiac muscle consumes the oxygen, but the long request rather selectivity
  • 匿名
2013-05-23 12:26:38
Typically, as preanesthetic medication of atropine to reduce glandular secretions, but atropine is a selective m receptor blockers, and increased heart rate after using, increased myocardial oxygen consumption, penehyclidine selective effects on M1,M3 receptors, on the M2 receptors almost had no eff
  • 匿名
2013-05-23 12:28:18
正在翻译,请等待...
 
 
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