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单词 COMT
释义

COMT

原声例句
Osmosis-神经

Alright the next dopamine-directed class of therapies are inhibitors of COMT, catecholamine-O-methyltransferase, which is an enzyme that degrades dopamine and levodopa.

下一个针对多巴胺的治疗药物是COMT抑制剂;COMT,即儿茶酚胺-O-甲基转移酶,是一种可以降解多巴胺和左旋多巴的酶。

医学英语视频

So, here another useful drugs come into play, namely Selegiline and Rasagiline, which selectively inhibit MAO-B, and Tolcapone, which inhibits COMT.

因此,另一种有用的药物开始发挥作用,即塞来吉林和拉沙吉林,它们选择性地抑制MAO-B和Tolcapone,后者抑制COMT。

医学英语视频

However, lets not forget that dopamine is also susceptible to breakdown by COMT as well as MAO-B, which convert dopamine to 3-methoxytyramine (3-MT) and 3,4dihydroxyphenylacetic acid (DOPAC) respectively.

然而,我们不要忘记多巴胺也容易被COMT分解如MAO-B,可将多巴胺转化为3-甲氧基酪胺(3-MT)和3,4-二羟基苯乙酸(DOPAC)分别。

医学英语视频

Finally, excess dopamine in the synapse is reuptaken back into the neuron, or into glial cells where it gets metabolized by Monoamine Oxidase (abbreviated MAO) and Catechol-O-methyltransferase (abbreviated COMT).

最后,突触中过量的多巴胺被重新吸收回神经元或胶质细胞由单胺氧化酶(简称MAO)和儿茶酚-O-甲基转移酶代谢的细胞(缩写COMT)。

Osmosis-神经

COMT inhibitors like entacapone and tolcapone are only given with levodopa to prevent the enzyme from breaking it down outside the central nervous system, thus allowing more of it to enter the brain.

COMT抑制剂,例如恩他卡朋和托卡朋与左旋多巴一起用于治疗,只是为了防止左旋多巴在中枢神经系统外被分解,从而使更多左旋多巴进入脑中。

医学英语视频

Another agent that is used in combination with Levodopa and Carbidopa is Entacapone, which inhibits peripheral COMT and thus just like Carbidopa, it prolongs the time that Levodopa is available to the brain.

另一种与左旋多巴和卡比多巴联合使用的药剂是恩他卡彭,它能抑制外周血细胞凋亡,因此就像卡比多巴一样,它延长了左旋多巴对大脑有效。

中文百科

儿茶酚-O-甲基转移酶 Catechol-O-methyl transferase

(重定向自COMT)

儿茶酚-O-甲基转移酶 (COMT; EC2.1.1.6)是分解儿茶酚胺(如多巴胺、肾上腺素和去甲肾上腺素)的几种酶之一。在人体,儿茶酚-O-甲基转移酶COMT基因编码。鉴于在一些疾病中儿茶酚胺的调节受损,数种药物以COMT为标靶,调整其活性来控制儿茶酚胺的浓度。

COMT在1957年由生物化学家 朱利叶斯·阿克塞尔罗德发现。

英语百科

Catechol-O-methyl transferase 儿茶酚-O-甲基转移酶

(重定向自COMT)

Catechol-O-methyltransferase (COMT; EC2.1.1.6) is one of several enzymes that degrade catecholamines such as dopamine, epinephrine, and norepinephrine. In humans, catechol-O-methyltransferase protein is encoded by the COMT gene. As the regulation of catecholamines is impaired in a number of medical conditions, several pharmaceutical drugs target COMT to alter its activity and therefore the availability of catecholamines. COMT was first discovered by the biochemist Julius Axelrod in 1957.

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更新时间:2025/6/22 13:01:36