槲皮素的药理作用机制及其在奶牛生产中的应用

2017-01-18 00:39郭长征冯泮飞毛胜勇
动物营养学报 2017年1期
关键词:槲皮素瘤胃奶牛

郭长征 冯泮飞 毛胜勇

(江苏省消化道营养与动物健康重点实验室,南京农业大学消化道微生物实验室,南京210095)



槲皮素的药理作用机制及其在奶牛生产中的应用

郭长征 冯泮飞 毛胜勇*

(江苏省消化道营养与动物健康重点实验室,南京农业大学消化道微生物实验室,南京210095)

槲皮素是中草药和果蔬等植物中常见的黄酮醇类物质,具有抗炎、抗菌、抗氧化、抗肿瘤及抗癌等广泛的药理活性。近年来在奶牛研究中发现,槲皮素可改善奶牛瘤胃发酵,对奶牛糖代谢及脂代谢具有一定影响。本文就槲皮素的药理作用机制及其在奶牛生产中的应用进展进行了综述,拟为槲皮素的进一步开发应用提供理论参考。

槲皮素;生物学作用;机制;奶牛

在现代集约化养殖业中,为最大程度地追求生产效益,在奶牛生产中常使用高比例精料[1];较高的能量摄入及较高的产奶量使奶牛机体氧化代谢增强,进而产生大量活性氧[2-3],造成机体出现氧化损伤。另外,我国南方夏季炎热高温引发的奶牛热应激问题也常导致动物自身的抗氧化能力下降[4-5],并对奶牛生产性能、繁殖性能及免疫性能等造成不利影响[6-8]。因此,如何提高动物抗氧化能力已成为当前奶牛生产的一个重要问题。槲皮素(quercetin,3,3’,4’,5,7-五羟基黄酮,图1)是植物界中分布最广的黄酮类化合物,可减少啮齿动物肝脂肪积聚预防脂肪肝发生[9-10],同时具有抗氧化、抗炎功能[11-12]。因此,一些研究者认为,开发基于槲皮素为基础的饲料添加剂对保障奶牛健康具有重要意义。本文在前人研究基础上,综述了槲皮素的药理作用机制及在奶牛生产上应用的初步进展,拟为槲皮素的应用开发提供理论参考。

1 槲皮素的药理作用及机制

1.1 槲皮素的抗炎作用及机制

研究发现,一些经典的炎性相关疾病如(类)风湿性关节炎、动脉粥样硬化和全身性炎症反应综合征等急慢性炎性疾病的发生或致病过程,均与核转录因子κB(NF-κB)过度或持续激活密切相关[13]。NF-κB可诱导细胞因子、趋化因子、黏附分子[如细胞间黏附分子-1(ICAM-1)、血管细胞黏附分子-1(VCAM-1)和内皮白细胞黏附分子1(ELAM1)]大量生成,同时激活一些与炎性级联放大相关的酶[如诱导型一氧化氮合酶(iNOS)和诱导型环氧化合酶]。Cho等[14]研究表明,槲皮素可抑制细胞外信号调节激酶(ERK)和p38丝裂原活化蛋白激酶(p38MAPK)的磷酸化,且通过稳定核转录因子κB/核转录因子κB抑制蛋白复合体(NF-κB/IκB)阻止核转录因子κB抑制蛋白(IκB)的脱落,抑制下游白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)及一氧化氮(NO)/iNOS的表达。Min等[15]发现,槲皮素可封阻p38MAPK和NFκB的活化,减少IL-1β、IL-6、TNF-α和白细胞介素-8(IL-8)的表达。此外,槲皮素可在转录和蛋白质水平抑制前炎症因子诱导VCAM-1、ICAM-1和单核细胞趋化蛋白(MCP-1)的表达与合成[16];抑制激活蛋白-1的活性和c-Jun氨基末端激酶(JNK)通路,减少佛波酯和TNF-α诱导人类内皮细胞ICAM-1的产生[17]。有研究显示,槲皮素还可抑制iNOS和环氧化合酶-2(COX-2)的表达[18-21]。槲皮素亦可抑制免疫细胞组胺酸脱羧酶的翻译[22]、组胺释放[23]及脱粒[24]。

图1 槲皮素的化学结构

1.2 槲皮素的抗氧化作用及机制

动物机体在代谢营养物质时,可产生大量自由基,正常情况下,自由基可被体内的防御体系清除;但当机体受损时,自由基可引起细胞薄膜脂质过氧化,导致细胞薄膜损伤,改变渗透压引起细胞肿胀,最终导致细胞死亡[25]。体内自由基的来源包括酶促反应与非酶促反应产生2种途径。酶促反应途径中,黄嘌呤氧化酶(XO)、脂氧化酶(LOX)、醛氧化酶(AO)等均为可催化产生自由基的氧化酶;非酶促反应途径是体内某些物质的自动氧化与分子氧的单电子还原途径,自动氧化如过渡金属离子的氧化还原及过氧化物均可产生自由基。目前发现,槲皮素可通过抑制自由基的产生、防止脂质过氧化、激活机体抗氧化体系等方式起到抗氧化作用。

1.2.1 抑制自由基的产生

研究表明,槲皮素可通过抑制黄嘌呤氧化酶活而抑制超氧化物产生[26-27]。Ratty等[28]用抗坏血酸维生素C和硫酸亚铁诱导小鼠脑线粒体脂质过氧化,探究槲皮素的抑制效应,结果表明,槲皮素可同时抑制前述2种诱导剂诱导脂质过氧化。

1.2.2 激活机体抗氧化体系

体内的抗氧化酶有超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)和过氧化氢酶(CAT)等。Coskun等[29]以链脲霉素诱导小鼠糖尿病为模型研究槲皮素添加效应,结果表明,小鼠注射链脲霉素可引起脂质过氧化,显著降低谷胱甘肽过氧化物酶、超氧化物歧化酶、过氧化氢酶活性,而槲皮素则显著提高了上述抗氧化酶的活性。

1.3 槲皮素的抗肿瘤作用及机制

1.3.1 抑制肿瘤细胞增殖

槲皮素对多种恶性肿瘤细胞均有抑制作用,如胃癌细胞(HGC-27、NUGE-2、MKN-7、MKN-28)[30]、结肠癌细胞(COLO320 DM)[30-31]、人乳癌细胞[31-32]、人鳞状细胞和胶质瘤细胞[33-34]、卵巢癌细胞[35]、人肝癌细胞和人胰腺癌细胞[32,36]。肿瘤细胞即使在氧供应充分的条件下,仍以糖酵解方式获取能量,称为有氧糖酵解,这既是著名的“Warburg效应”。槲皮素抑制肿瘤细胞增殖的原因可能是阻止了肿瘤细胞有氧糖酵解[37]。

1.3.2 诱导肿瘤细胞凋亡

有研究表明,槲皮素可通过激活内部线粒体途径促进肿瘤细胞凋亡。当细胞受到内部凋亡刺激因子作用,凋亡因子Bax、Bak等受到激活结合到线粒体外膜,在膜上形成线粒体内部通向胞质的孔道,致使细胞色素C等进入细胞质。细胞色素C激活凋亡酶激活因子-1(APAF-1),APAF-1可活化含半胱氨酸的天冬氨酸蛋白水解酶-9(caspase-9)。细胞色素C、APAF-1、caspase-9组成凋亡小体,该凋亡小体具有裂解凋亡蛋白酶含半胱氨酸的天冬氨酸蛋白水解酶-7(caspase-7)的作用,caspase-7裂解激活后引起下游与细胞生命相关蛋白质的降解,最终引起细胞凋亡。B淋巴细胞瘤-2(Bcl-2)、髓样细胞白血病-1(Mcl-1)、B淋巴细胞瘤-xL(Bcl-xL)可通过抑制Bax、Bak作用,发挥抗凋亡作用[38]。研究表明,槲皮素可下调多种癌细胞Bcl-2、Mcl-1、Bcl-xL水平,上调Bax水平,并激活下游通路,促进细胞凋亡,从而起到抗肿瘤作用[39-47]。

1.3.3 抑制肿瘤细胞转移、侵袭

肿瘤侵袭和转移的关键步骤是降解肿瘤周围的基质,基质金属蛋白酶(MMP)能通过破坏基质的降解平衡,进而促进癌细胞突破基底膜和细胞外基质构成的组织学屏障,从而侵袭周围组织和转移至远处组织。有研究表明,槲皮素可通过蛋白激酶C(PKC)通路下调基质金属蛋白酶前体-9(Pro-MMP-9)[48];减少MMP-2、MMP-9的分泌[32,36];抑制MMP-2、MMP-9的活性[49],从而抑制癌细胞的侵袭。

2 槲皮素在奶牛生产上的应用进展

2.1 槲皮素的生物利用率

奶牛不同于单胃动物,其瘤胃内栖息着各种微生物,包括瘤胃原虫、瘤胃细菌、和厌氧真菌,还有少数噬菌体[50]。槲皮素是否能够有效进入奶牛外周循环,是其在奶牛上能否发挥出在单胃动物上功能的前提。通过瘤胃瘘管添加槲皮素的动力学试验表明,总黄酮醇(结合与非结合形式槲皮素及结合与非结合形式的槲皮素衍生物之和)的绝对生物利用率仅为0.1%[51]。有研究表明,槲皮素被瘤胃微生物迅速降解成3,4-二羟基苯乙酸和4-甲基邻苯二酚[52],这可能是生物利用率低的原因。而通过奶牛十二指肠添加槲皮素接近猪等单胃动物口服添加下的生物利用率[53]。因此,过瘤胃添加槲皮素更能发挥其在奶牛生产中的作用。

2.2 槲皮素对瘤胃发酵的影响

槲皮素对变异链球菌、血链球菌、嗜酸乳杆菌和远缘链球菌有抑制效应[54],暗示其可能通过改变瘤胃微生物菌群从而调控瘤胃发酵。瘤胃是反刍动物消化代谢和营养物质吸收最重要的场所,饲粮中碳水化合物在瘤胃内被瘤胃微生物发酵产生挥发性脂肪酸(VFA),VFA可为宿主提供60%~80%的能量[55]。瘤胃发酵体外模拟试验表明,添加不同剂量槲皮素瘤胃发酵参数不一致。添加500 mg/L槲皮素可显著增加总挥发性脂肪酸(TVFA)浓度[56],作者认为槲皮素刺激了瘤胃发酵。其他研究表明,添加量为4.5%底物时,槲皮素对pH、TVFA浓度、单一VFA比例无显著影响[57];槲皮素对干物质降解率及羧甲基纤维素酶、木聚糖酶、β-葡萄糖苷酶活性无显著影响,说明槲皮素并不能改变瘤胃对营养物质的发酵程度[57];另外,最近的研究表明,槲皮素可被瘤胃微生物迅速降解,通过奶牛瘤胃瘘管添加50 mg/kg BW的槲皮素对TVFA浓度及各单一VFA比例也无显著影响[52]。此外,与体外发酵相比,瘤胃添加槲皮素被快速吸收入血液或降解;而体外发酵槲皮素不能向肠道外流。因此,部分研究中添加槲皮素显著增加TVFA浓度的结果,可能是槲皮素被瘤胃微生物降解利用造成的。

有研究认为,对于减少甲烷产生,植物次级代谢物相比于离子载体和益生菌具有价格低廉及环保的优势[58],具有作为抑制甲烷产生的添加剂的潜力,槲皮素是其中分布最广的类黄酮[59]。目前体外发酵试验表明,槲皮素添加量为4.5%底物时,可增加产气量,减少甲烷产量,降低原虫、产甲烷菌数量[57];培养基中添加100 μmol/L的槲皮素对产气量及甲烷产量无显著影响[52]。结果不一可能是试验条件及添加量不同所致。Leiber等[60]研究发现,添加芦丁(5和500 μmol/L的槲皮素)可显著增加产气量,但是其中甲烷比例下降,作者认为芦丁被非产甲烷微生物作为底物产生CO2,从而降低了总产气中甲烷的比例。综上,槲皮素对于产气量和甲烷含量的影响及机制还需进一步研究确定;槲皮素对除原虫、产甲烷菌外的瘤胃微生物无抑制作用。

2.3 槲皮素对奶牛机体健康的影响

围产期奶牛采食摄入的能量不足以满足泌乳需要,奶牛动用体脂供能,当肝脏吸收的脂质超过其氧化和分泌时发生脂肪肝[1]。有研究表明,约有50%的奶牛可发生脂肪肝同时伴随肝细胞损害及肝功能下降[61-62]。另外,由于围产期奶牛大量的能量摄入及泌乳造成氧化代谢增强,产生更多活性氧[2-3]。研究发现,槲皮素可减少啮齿动物肝脏脂肪积聚及预防脂肪肝发生[10]。由此,结合槲皮素的保肝作用及抗炎、抗氧化作用,一些学者对槲皮素在奶牛上的作用进行了初步研究。连续28 d通过十二指肠瘘管添加36 mg/kg BW的槲皮素对奶牛超氧化物歧化酶、谷胱甘肽过氧化物酶和过氧化氢酶活性均无显著影响[63]。原因可能在于以下2点:1)槲皮素添加剂量少,添加100 mg/kg BW的槲皮素在mRNA水平上显著提高了奶牛超氧化物歧化酶表达量[64];2)槲皮素的抗氧化作用与机体健康程度有关,槲皮素对链霉素诱导的糖尿病、人造肝脏损伤有积极作用[65-67],而对健康小鼠超氧化物歧化酶和过氧化氢酶活性无影响[68]。

槲皮素可提高血液中胰岛素含量,降低葡萄糖含量,与在人糖尿病中的作用一致[69]。但是对于糖代谢相关基因(葡萄糖6磷酸酶、丙酮酸羧化酶和磷酸烯醇式丙酮酸羧化酶)则无显著影响。有报道表明,槲皮素可抑制肠细胞对葡萄糖的吸收而提高肌细胞的吸收[70-71]。因此槲皮素可能通过促进胰岛素的分泌及其他组织对葡萄糖的吸收降低血液葡萄糖含量。

重度脂肪浸润可导致肝细胞破坏,随后引起胞浆天冬氨酸转氨酶释放[69]。谷氨酸脱氢酶主要存在于肝脏中,其血液中含量升高暗示肝细胞死亡或亚致死损伤[72]。有研究表明,槲皮素可显著降低奶牛血液中天冬氨酸转氨酶含量,虽然血液中谷氨酸脱氢酶含量统计学上变化不显著,但是未添加槲皮素奶牛分娩后比分娩前谷氨酸脱氢酶含量增加了300%,而添加槲皮素奶牛仅增加了50%[73]。此结果表明,槲皮素具有减少肝损害的作用。另外,槲皮素具有减少肝脏脂肪含量的趋势[64]。因此,槲皮素可能通过减少肝细胞损害,保护肝细胞的正常功能而减少肝脏脂肪含量。

2.4 槲皮素对奶牛生产性能及蹄部健康的影响

饲粮中添加槲皮素可提高泌乳中期奶牛的乳蛋白含量,但对乳脂、乳糖含量无影响[63]。作者认为这可能与槲皮素增加血液中胰岛素含量有关。有研究表明,静脉灌注胰岛素可提高奶牛乳蛋白含量[74]。而在奶牛瘤胃中长期灌注芦丁(槲皮素糖苷衍生物),可使奶牛产奶量提高10.06%,但对乳品质无显著影响[75]。

MMP主要功能是降解细胞外基质和基膜,奶牛蹄组织中存在MMP,在健康状况下,MMP基因的表达及活性均受到严格的调控,但在亚急性瘤胃酸中毒条件下,奶牛蹄组织中MMP-2和MMP-9的活性上调,进而催化降解基膜等重要结构,使蹄叶组织失去正常的连接、渗透与屏障功能,最终导致真皮小叶与角小叶发生渗出性炎症,形成蹄叶炎[76]。槲皮素抗肿瘤作用中显示,槲皮素可抑制MMP-2和MMP-9上游通路,阻止其分泌并抑制其活性。因此,槲皮素可能具有预防蹄叶炎的作用。但在奶牛上的研究发现,槲皮素对MMP-2和MMP-9表达无显著影响,仅对奶牛蹄白线分离有改善作用[77]。原因可能是,槲皮素对MMP-2和MMP-9抑制基本为离体试验,而奶牛上的研究中槲皮素添加形式为口服,槲皮素可能被瘤胃微生物降解造成生物利用率低。因此,未来有必要开展蹄组织体外培养的研究,以确定槲皮素是否具有预防蹄叶炎的作用,以期为研究有效的过瘤胃槲皮素奠定基础。

3 小 结

槲皮素是黄酮类化合物中一种天然植物提取物,具有抗炎、抗氧化及抗肿瘤等功能。槲皮素在奶牛生产上的研究还处于初步阶段,对抑制甲烷产生、减少肝脏脂肪积聚、减少肝损伤、提高乳蛋白含量及预防蹄叶炎方面体现出较大潜力。但是由于槲皮素可被瘤胃微生物降解且上述试验中试验动物偏少,因此开发过瘤胃形式槲皮素、开展大规模动物试验进一步验证槲皮素在奶牛生产上的作用很有必要。

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*Corresponding author, professor, E-mail: maoshengyong@163.com

(责任编辑 王智航)

Quercetin: Pharmacological Action Mechanism and Application in Dairy Cows Production

GUO Changzheng FENG Panfei MAO Shengyong*

(JiangsuKeyLaboratoryofGastrointestinalNutritionandAnimalHealth,LaboratoryofGastrointestinalMicrobiology,NanjingAgriculturalUniversity,Nanjing210095,China)

Quercetin is a common flavonoid in herbs, fruits and vegetables, and has anti-inflammatory, antibacterial, antioxidant, anti-tumor and anti-cancer and other pharmacological activities. In recent years, studies found that quercetin addition could improve rumen fermentation of dairy cows, and could affect glucose metabolism and lipid metabolism. In this paper, the pharmacological mechanism of quercetin and its application in dairy cows production were reviewed to provide reference for the further development and application.[ChineseJournalofAnimalNutrition, 2017, 29(1):42-49]

quercetin; biochemical function; mechanism; dairy cow

10.3969/j.issn.1006-267x.2017.01.006

2016-07-12

国家自然科学基金项目(31372339)

郭长征(1992—),男,河南濮阳人,硕士研究生,从事反刍动物营养研究。E-mail: 2014105044@njau.edu.cn

*通信作者:毛胜勇,教授,博士生导师,E-mail: maoshengyong@163.com

S816.7;S823

A

1006-267X(2017)01-0042-08

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