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大鼠肝脏中一种N-甲基转移酶催化的肾上腺素合成。

Epinephrine synthesis by an N-methyltransferase in rat liver.

作者信息

Elayan H, Kennedy B, Ziegler M G

机构信息

Department of Medicine, University of California San Diego Medical Center.

出版信息

Gastroenterology. 1990 Jan;98(1):152-5. doi: 10.1016/0016-5085(90)91304-o.

Abstract

We investigated if liver can synthesize epinephrine in vitro and in vivo. Homogenates of rat liver readily synthesized [3H]epinephrine from [3H]S-adenosylmethionine and norepinephrine. Liver homogenates also N-methylated dopamine at more than twice the rate that they N-methylated norepinephrine. In contrast, adrenal homogenates, which N-methylate norepinephrine to form epinephrine using the enzyme phenylethanolamine-N-methyltransferase (PNMT), methylated dopamine only about 1% as well as norepinephrine. Synthesis of epinephrine by liver homogenates was not significantly inhibited by the PNMT inhibitor SKF 29661 at a concentration that inhibited adrenal homogenate epinephrine synthesis by nearly 90%. These findings indicate that liver can synthesize epinephrine in vitro using an enzyme other than PNMT. Adrenal demedullation of rats reduced plasma epinephrine levels to 7% of control values, but left liver epinephrine and epinephrine-forming enzyme levels unchanged. Treatment of demedullated rats with 6-hydroxydopamine plus reserpine also resulted in dramatically reduced plasma epinephrine levels but no change in hepatic epinephrine and N-methylating enzyme levels. We conclude that the liver synthesizes its own epinephrine.

摘要

我们研究了肝脏在体外和体内是否能够合成肾上腺素。大鼠肝脏匀浆能够轻易地从[3H]S-腺苷甲硫氨酸和去甲肾上腺素合成[3H]肾上腺素。肝脏匀浆将多巴胺N-甲基化的速率是将去甲肾上腺素N-甲基化速率的两倍多。相比之下,肾上腺匀浆利用苯乙醇胺-N-甲基转移酶(PNMT)将去甲肾上腺素N-甲基化形成肾上腺素,其将多巴胺N-甲基化的能力仅为去甲肾上腺素的1%左右。肝脏匀浆合成肾上腺素的过程不会被PNMT抑制剂SKF 29661显著抑制,而该浓度的SKF 29661可使肾上腺匀浆的肾上腺素合成受到近90%的抑制。这些发现表明,肝脏可在体外利用PNMT以外的一种酶合成肾上腺素。大鼠肾上腺髓质切除使血浆肾上腺素水平降至对照值的7%,但肝脏中的肾上腺素及肾上腺素形成酶水平未变。用6-羟基多巴胺加利血平处理去髓质大鼠也导致血浆肾上腺素水平显著降低,但肝脏中的肾上腺素及N-甲基化酶水平未变。我们得出结论,肝脏能够合成自身的肾上腺素。

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