cardiovascular neurasthenia

cardiovascular neurasthenia的基本解释

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[医] 心血管神经衰弱

与cardiovascular neurasthenia相关的网络例句 [注：此内容来源于网络，仅供参考]

This research method is to use the three-dimensional mapping software to draw the cardiovascular stent of different size first , next is it create their cardiovascular stent boundary conditions and simulation their of support after implantation according to finite element method into the human body to go; Receive different residue pressures and pressure of the repeated blood circulation , greatest stress , meets an emergency and the relation between total deformation amount caused; Being imitated the cardiovascular stent , the position with damage of fatigue life in the blood vessel by its greatest stress value at the same time ; But by the simulation result of the above , can understand that use life of Palmaz-schatz cardiovascular stent has been more than 109 up till now ; At the same time , can know the position where the stress two times concentrates , the right angle position joined in the rib and rib of Palmaz-schatz cardiovascular stent too.

本研究的方法乃是先会使用三维绘图软体画出不同尺寸的血管支架，然后在根据有限元素法去设定其血管支架的边界条件和模拟其植入人体后；受到不同的残留压力与反覆血液流动的压力，所造成的最大应力、应变及总变形量之间的关系；同时在由其最大应力值去模拟血管支架，在血管中的疲劳寿命与疲劳损坏位置；然而由以上的模拟结果，可以了解到目前Palmaz-schatz血管支架之使用寿命为109以上；同时也可以知道二次应力集中的位置，在Palmaz-schatz血管支架之肋和肋连接的直角位置。

To Explore the personality traits of university students with neurasthenia and non-neurasthenia.

目的：探讨神经衰弱和非神经衰弱大学生个性特征及康复措施。

In clinical. acetylcholinesterase inhibitors reduce the breakdown of synaptic acetylcholine, have been modestly effective in improving the cognitive deficits of Alzheimer's disease.The goal of this work is to determine enzyme kinetics and mechanisms of acetylcholinesterase and butyrlcholinesterase inhibition by five cardiovascular drugs, lovastatin, simvastatin, amlodipine besylate, nifedipine, and hydralazine hydrochloride, and two benzodiazepines, diazepam and chlordiazepoxide hydrochloride. All drugs in this study are reversible mixed-type inhibitors of acetylcholinesterase and butyrylcholinesterase. The pKi values for acetylcholinesterase and butyrylcholinesterase inhibition by the cardiovascular drugs are linearly correlated with the molecular weights of the drugs with the slopes of 0.005 and 0.0021, respectively. Therefore, van der Waals' interactions between acetylcholinesterase and the cardiovascular drugs are stronger than those between butyrylcholinesterase and the drugs. This is probably due to a smaller active site gorge and a more significant peripheral anionic substrate binding site of acetylcholinesterase than those of butyrylcholinesterase.

本研究之目的系决定乙醯胆碱酯酵素和丁醯胆碱酯酵素被五种心脏血管药物lovastatin， simvastatin， amlodipine besylate， nifedipine、hydralazine hydrochloride和两种benzodiazepines：diazepam和Chlordiazepoxide hydrochloride的抑制作用之动力学及机转，这些药物都是乙醯胆碱酯酵素和丁醯胆碱酯酵素的可逆性、混合型之抑制剂，实验结果显示，五种心血管药物对於乙醯胆碱酯酵素及丁醯胆碱酯酵素抑制之pKi值和药物之分子量呈直线之关系，斜率分别为0.005及0.0021因此丁醯胆碱酯酵素，与心血管药物间之凡德瓦作用（van der Waals' ）比乙醯胆碱酯酵素与心血管药物间者弱，这可能原因是丁醯胆碱酯酵素之活性区域比乙醯胆碱酯酵素之活性区域更宽广，但丁醯胆碱酯酵素之周边阴离子区域不及乙醯胆碱酯酵素之周边阴离子区域者明显重要，由於五种心血管药物对於乙醯胆碱酯酵素和丁醯胆碱酯酵素抑制之pKi值存在著线性关系表示此种抑制作用系经过共同之反应机理。

与cardiovascular neurasthenia相关的网络解释 [注：此内容来源于网络，仅供参考]

Neurasthenia universalis：一般神经衰弱,普遍性神经衰弱

交感性神经衰弱 Neurasthenia sympathica | 一般神经衰弱,普遍性神经衰弱 Neurasthenia universalis | 血管运动性神经衰弱 Neurasthenia vasomtoria ; Vasomotor neurasthenia

Neurasthenia sympathica：交感性神经衰弱

脊髓性神经衰弱 Neurasthenia spinalis ; Spinal neurasthenia ; Spinal irritation | 交感性神经衰弱 Neurasthenia sympathica | 一般神经衰弱,普遍性神经衰弱 Neurasthenia universalis

cardiovascular specialist：心思以及精力管专业人士

cardiovascular scissors 心思以及精力管剪 | cardiovascular specialist 心思以及精力管专业人士 | cardiovascular system 心思以及精力管体系