儿茶酚胺




兒茶酚胺(拉丁語:Catecholamine)是具有兒茶酚核的(苯乙)胺類化合物的統稱,是由腎上腺產生的一類應激擬交感「鬥或逃」(Fight or Flight)激素。最重要的兒茶酚胺是腎上腺素(Epinephrine)、去甲腎上腺素(正腎上腺素)和多巴胺(Dopamine),均是從苯丙氨酸和酪氨酸合成。去甲腎上腺素在中樞神經系統內分布廣泛,含量較多,而腎上腺素含量則較少。多巴胺主要集中在錐體外系部位,也是一種神經介質。它們是重要的典型的腎上腺素受體激動劑。不少精神興奮劑也是兒茶酚胺的類似物。


兒茶酚胺有去甲腎上腺素(NAd)、腎上腺素(Ad)、多巴胺(DA),過多的兒茶酚胺分泌可能導致高血壓和心肌梗塞。而低水平的兒茶酚胺可能引起低血壓、心肌缺血等的發生
、在臨床上兒茶酚胺常被用來治療神經源性、心源性、中毒源性休克早期,但過多剂量可能導致局部組織壞死或者腎臟衰竭。




經由L-酪氨酸,兒茶酚胺的生物合成。




目录






  • 1 化學結構


  • 2 图集


  • 3 参考文献


  • 4 外部链接





化學結構





人腦中儿茶酚胺&痕量胺的合成路徑[1][2][3]


Graphic of catecholamine and trace amine biosynthesis


苯丙氨酸

酪氨酸

L-多巴

肾上腺素

苯乙胺

酪胺

多巴胺

去甲肾上腺素

N-二甲基苯乙胺英语N-Methylphenethylamine

N-甲基酪胺英语N-Methyltyramine

章胺

辛弗林

3-甲氧酪胺英语3-Methoxytyramine

AADC

AADC

AADC

primary
pathway

PNMT

PNMT

PNMT

PNMT

AAAH英语Biopterin-dependent aromatic amino acid hydroxylase

AAAH英语Biopterin-dependent aromatic amino acid hydroxylase

brain
CYP2D6

minor
pathway

COMT

DBH

DBH




图像顶端包含可点击的链接
人體中的兒茶酚胺及苯乙胺都是起源自氨基酸





图集




参考文献





  1. ^ Broadley KJ. The vascular effects of trace amines and amphetamines. Pharmacol. Ther. March 2010, 125 (3): 363–375. PMID 19948186. doi:10.1016/j.pharmthera.2009.11.005. 


  2. ^ Lindemann L, Hoener MC. A renaissance in trace amines inspired by a novel GPCR family. Trends Pharmacol. Sci. May 2005, 26 (5): 274–281. PMID 15860375. doi:10.1016/j.tips.2005.03.007. 


  3. ^ Wang X, Li J, Dong G, Yue J. The endogenous substrates of brain CYP2D. Eur. J. Pharmacol. February 2014, 724: 211–218. PMID 24374199. doi:10.1016/j.ejphar.2013.12.025. The highest level of brain CYP2D activity was found in the substantia nigra ... The in vitro and in vivo studies have shown the contribution of the alternative CYP2D-mediated dopamine synthesis to the concentration of this neurotransmitter although the classic biosynthetic route to dopamine from tyrosine is active. ... Tyramine levels are especially high in the basal ganglia and limbic system, which are thought to be related to individual behavior and emotion (Yu et al., 2003c). ... Rat CYP2D isoforms (2D2/2D4/2D18) are less efficient than human CYP2D6 for the generation of dopamine from p-tyramine. The Km values of the CYP2D isoforms are as follows: CYP2D6 (87–121 μm) ≈ CYP2D2 ≈ CYP2D18 > CYP2D4 (256 μm) for m-tyramine and CYP2D4 (433 μm) > CYP2D2 ≈ CYP2D6 > CYP2D18 (688 μm) for p-tyramine 




外部链接



  • MeSH(醫學主題詞)上面的Catecholamines(美式英语)









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