新冠肺炎“炎癥風(fēng)暴”是近期公眾關(guān)注的諸多熱點(diǎn)話題之一;所謂“炎癥風(fēng)暴”即全身炎癥反應(yīng)綜合征(SIRS),人體的炎癥因子,不僅可以殺掉病毒,也會(huì)給自身造成損害,某些新冠患者后期可能突然啟動(dòng)了一個(gè)“炎癥風(fēng)暴”,結(jié)果導(dǎo)致各個(gè)器官的功能衰竭。那么應(yīng)該如何應(yīng)對(duì)“炎癥風(fēng)暴”呢?中南大學(xué)湘雅醫(yī)學(xué)院林韶輝博士撰文“有效針對(duì)新冠肺炎的“炎癥風(fēng)暴”——Omega-3多不飽和脂肪酸”,表達(dá)了自己的一些觀點(diǎn),或許會(huì)給大家一些思考和啟發(fā)。
一、新冠肺炎專家說
1. 武漢金銀潭醫(yī)院:上海中山醫(yī)院重癥醫(yī)學(xué)科副主任鐘鳴醫(yī)生(2020年1月24到達(dá)武漢),2020年2月3日,南方人物周刊對(duì)鐘醫(yī)生進(jìn)行獨(dú)家專訪,提到救治初期,所面臨的困難之中,有的新冠患者后期可能突然啟動(dòng)了一個(gè)“炎癥風(fēng)暴”,這種炎癥風(fēng)暴導(dǎo)致了各個(gè)器官的功能衰竭,一旦進(jìn)入這個(gè)狀態(tài),我們的治療很難把它拉回來。
2. 武漢大學(xué)中南醫(yī)院:《美國(guó)醫(yī)學(xué)會(huì)雜志》2月7日在線發(fā)布了武漢大學(xué)中南醫(yī)院重癥監(jiān)護(hù)室(ICU)主任彭志勇博士領(lǐng)銜的一項(xiàng)回顧性分析,研究團(tuán)隊(duì)認(rèn)為,新冠肺炎致死的三大主要機(jī)制:
中性粒細(xì)胞增多,與細(xì)胞因子風(fēng)暴有關(guān);
D-二聚體升高反映凝血激活,提示持續(xù)的炎癥反應(yīng);
血尿素升高提示急性腎損傷,這是感染、休克和缺氧的綜合結(jié)果。
3. 種種跡象表明,這些重癥患者中發(fā)生了不可逆轉(zhuǎn)的“炎癥風(fēng)暴”。而一旦患者發(fā)生“炎癥風(fēng)暴”,糖皮質(zhì)激素是對(duì)抗炎癥風(fēng)暴的武器之一,可以給免疫系統(tǒng)“滅火”,減輕機(jī)體損傷。不過,糖皮質(zhì)激素是一把“雙刃劍”。一方面它可以減輕炎癥反應(yīng),有利于改善缺氧、呼吸窘迫癥狀;但長(zhǎng)期大劑量使用也可能引發(fā)諸多不良反應(yīng)。不少經(jīng)過大劑量激素治療的“非典”患者,都留下了如股骨頭壞死等嚴(yán)重后遺癥。
二、“炎癥風(fēng)暴”與Omega-3多不飽和脂肪酸
3. Omega-3 PUFA對(duì)抗炎癥反應(yīng)的作用機(jī)制
圖1. 長(zhǎng)鏈不飽和脂肪酸代謝示意圖
4. 多種文獻(xiàn)證明,為了減少患者還可能發(fā)生爆發(fā)性炎癥反應(yīng),使用高純度的 Omega-3 PUFA制劑,可以減低炎癥風(fēng)暴的發(fā)生風(fēng)險(xiǎn)。具體表現(xiàn)
4.1 Omega-3 PUFA富集于細(xì)胞膜,參與炎癥反應(yīng)調(diào)控過程,減少炎性細(xì)胞產(chǎn)生促炎性細(xì)胞因子;
Omega-3 PUFA富集于細(xì)胞膜,提高細(xì)胞膜EPA和DHA脂肪酸的比例[11, 12],影響胞內(nèi)信號(hào)傳導(dǎo),抑制炎癥相關(guān)的轉(zhuǎn)錄因子NF-kappa B的轉(zhuǎn)錄活性[13, 14],從而減少促炎性細(xì)胞因子TNF-alpha、IL-6 和IL-8等的表達(dá)[15]。
花生四烯酸類脂質(zhì)經(jīng)一系列酶催化產(chǎn)生促炎癥調(diào)節(jié)作用的前列腺素(PGE2)和白三烯B4等。這些促炎性介質(zhì)進(jìn)而可激活中性粒細(xì)胞、巨噬細(xì)胞,刺激炎癥細(xì)胞因子TNF-α、IL-1、IL-2、IL-8和干擾素(Interferon, IFN)等釋放增多。Omega-3和Omega-6兩類 PUFA競(jìng)爭(zhēng)相同的脂肪酸代謝酶(Elovl5和FADS2)系統(tǒng)[16-18],從而干擾促炎性介質(zhì)的生成。
EPA和DHA經(jīng)代謝產(chǎn)生消散素(Resolvins)和保護(hù)素(Protections)。實(shí)驗(yàn)研究證實(shí),消散素和保護(hù)素在關(guān)節(jié)炎[19]、結(jié)腸炎[20]、哮喘[21, 22]等多種炎性疾病中發(fā)揮重要的抗炎作用[23, 24] 。例如,resolvin E1,resolvin D1和protectin D1能抑制浸潤(rùn)性中性粒細(xì)胞的細(xì)胞遷移,從而減輕局部炎癥[24]。此外,resolvin D1和protectin D1還能抑制TNF-α and IL-1β的產(chǎn)生,從而減弱炎癥反應(yīng)[25, 26]。
5. Omega-3 PUFA緩解炎癥的具體臨床獲益
5.1 C反應(yīng)蛋白等炎癥指標(biāo)顯著下降,血紅蛋白和白細(xì)胞、血小板等細(xì)胞類群總量顯著上升。
表1. ICU患者使用Omega-3 PUFA帶來的生理指標(biāo)和臨床指標(biāo)獲益
5.2 敗血癥狀明顯下降,治療用抗生素使用時(shí)間縮短,全身炎癥反應(yīng)綜合征減少,器官功能障礙后遺癥發(fā)生率減少,死亡率下降;
美國(guó)田納西大學(xué)附屬醫(yī)院和西班牙多所醫(yī)院的臨床研究表明,對(duì)于重癥創(chuàng)傷患者和膿毒癥患者等ICU患者,每天1~3克Omega-3 PUFA營(yíng)養(yǎng)液可以有效降低菌血癥、敗血癥并發(fā)癥發(fā)生(下降14%[29]~35%[30]),明顯降低治療用抗生素使用時(shí)間和腹腔內(nèi)膿腫發(fā)生率[30]。而使用更高Omega-3 PUFA含量(4克以上)的營(yíng)養(yǎng)液后,創(chuàng)傷病人全身炎癥反應(yīng)綜合征發(fā)生人數(shù)顯著下降[27];膿毒癥、敗血癥患者的器官功能障礙發(fā)生率減少達(dá)到43%[31],死亡率顯著下降13.1%[29]~19.4%[31]。
表2. 創(chuàng)傷患者和敗血癥患者使用Omega-3 PUFA的臨床獲益
5.3 改善氧合狀態(tài),減少呼吸機(jī)使用,縮短ICU監(jiān)護(hù)時(shí)間;
6.2 生物利用度高,保證體內(nèi)有效富集。
6.3 添加中鏈甘油三酯(MCTs),促進(jìn)Omega-3 PUFA快速細(xì)胞富集,為重癥患者的癥狀緩解贏得時(shí)間。添加MCT的Omega-3脂肪乳的體內(nèi)富集時(shí)間更短(術(shù)后第六天即檢測(cè)到病患血清磷脂和紅細(xì)胞細(xì)胞膜中的EPA和DHA顯著升高)[35],激發(fā)免疫更強(qiáng)(第六天起外周血細(xì)胞釋放的白三烯B5含量已增長(zhǎng)約2倍)[36];
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