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本文引用的文献

1
Chronotherapeutic effect of fisetin on expression of urea cycle enzymes and inflammatory markers in hyperammonaemic rats.水黄皮素对高血氨症大鼠尿素循环酶和炎症标志物表达的时间治疗效应。
Pharmacol Rep. 2014 Dec;66(6):1037-42. doi: 10.1016/j.pharep.2014.06.018. Epub 2014 Jul 8.
2
Effect of glutamine synthetase inhibition on brain and interorgan ammonia metabolism in bile duct ligated rats.谷氨酰胺合成酶抑制对胆管结扎大鼠脑和器官间氨代谢的影响。
J Cereb Blood Flow Metab. 2014 Mar;34(3):460-6. doi: 10.1038/jcbfm.2013.218. Epub 2013 Dec 18.
3
Ammonia production, excretion, toxicity, and defense in fish: a review.鱼类的氨生成、排泄、毒性和防御:综述。
Front Physiol. 2010 Oct 4;1:134. doi: 10.3389/fphys.2010.00134. eCollection 2010.
4
Marked potentiation of cell swelling by cytokines in ammonia-sensitized cultured astrocytes.细胞因子在氨敏培养星形胶质细胞中显著增强细胞肿胀。
J Neuroinflammation. 2010 Oct 13;7:66. doi: 10.1186/1742-2094-7-66.
5
Signaling pathways associated with inflammatory bowel disease.与炎症性肠病相关的信号通路。
Recent Pat Inflamm Allergy Drug Discov. 2010 Jun;4(2):105-17. doi: 10.2174/187221310791163071.
6
Hepatic encephalopathy, ammonia, glutamate, glutamine and oxidative stress.肝性脑病、氨、谷氨酸、谷氨酰胺与氧化应激
Ann Hepatol. 2009 Apr-Jun;8(2):95-102.
7
Identifying the direct effects of ammonia on the brain.确定氨对大脑的直接影响。
Metab Brain Dis. 2009 Mar;24(1):95-102. doi: 10.1007/s11011-008-9112-7. Epub 2008 Dec 23.
8
NFkappaB in the mechanism of ammonia-induced astrocyte swelling in culture.核因子κB在体外培养中氨诱导星形胶质细胞肿胀机制中的作用
J Neurochem. 2008 Sep;106(6):2302-11. doi: 10.1111/j.1471-4159.2008.05549.x. Epub 2008 Jul 4.
9
Pathogenetic mechanisms of hepatic encephalopathy.肝性脑病的发病机制。
Gut. 2008 Aug;57(8):1156-65. doi: 10.1136/gut.2007.122176.
10
Brain regional alterations in the modulation of the glutamate-nitric oxide-cGMP pathway in liver cirrhosis. Role of hyperammonemia and cell types involved.肝硬化时谷氨酸-一氧化氮-环磷酸鸟苷途径调节中的脑区改变。高氨血症的作用及相关细胞类型。
Neurochem Int. 2006 May-Jun;48(6-7):472-7. doi: 10.1016/j.neuint.2005.10.014. Epub 2006 Mar 6.

生物类黄酮槲皮素对高氨血症大鼠尿素循环酶、星形胶质细胞标志物和炎症标志物表达的作用

Role of Bioflavonoid Quercetin on Expression of Urea Cycle Enzymes, Astrocytic and Inflammatory Markers in Hyperammonemic Rats.

作者信息

Kanimozhi Sivamani, Subramanian Perumal, Shanmugapriya Sakkaravarthy, Sathishkumar Subramanian

机构信息

Department of Biochemistry and Biotechnology, Faculty of Science, Annamalai University, Chidambaram, Tamil Nadu 608 002 India.

出版信息

Indian J Clin Biochem. 2017 Mar;32(1):68-73. doi: 10.1007/s12291-016-0575-8. Epub 2016 May 5.

DOI:10.1007/s12291-016-0575-8
PMID:28149015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5247373/
Abstract

This study evaluates the role of quercetin on the expression of urea cycle enzymes, astrocytic, neuronal and inflammatory markers in hyperammonemic rats. Hyperammonemia (provoked by intraperitonial injections of (ammonium chloride-100 mg/kg b.w for 56 days), showed diminished expression of urea cycle enzymes [carbamyl phosphate synthetase-1 (CPS-1), ornithine transcarbamylase (OTC), argininosuccinate synthetase (ASS) and arginase (ARG)] in liver and decreased expression of neuronal and astrocytic markers-glutamine synthase (GS) and phosphate activated glutaminase (PAG) in brain and increased expression of brain inflammatory markers such as interleukin 6 (IL6), inducible nitric oxide synthase (iNOS) and nuclear transcription factor kappa B (NF-κB) (by western blot analysis) and exhibited downregulated expression of soluble guanylate cyclase (sGC), glial fibrillary acidic protein (GFAP) in brain and ASS in liver investigated (by RT-PCR). Oral treatment of quercetin (50 mg/kg b.w) to hyperammonemic rats (1) increased the expression of urea cycle enzymes (CPS-1, OTC, ASS and ARG), neuronal and astrocytic markers (GS and PAG) (2) decreased the expression of IL6, iNOS and NF-κB and (3) upregulated mRNA expression of SGC, GFAP and ASS. Our results specify that quercetin's antihyperammonemic effects could be through its, anti-inflammatory, neuroprotective and hepatoprotective effects.

摘要

本研究评估了槲皮素对高氨血症大鼠尿素循环酶、星形胶质细胞、神经元及炎症标志物表达的作用。高氨血症(通过腹腔注射氯化铵-100mg/kg体重,持续56天诱发)显示,肝脏中尿素循环酶[氨甲酰磷酸合成酶-1(CPS-1)、鸟氨酸转氨甲酰酶(OTC)、精氨琥珀酸合成酶(ASS)和精氨酸酶(ARG)]的表达降低,大脑中神经元和星形胶质细胞标志物——谷氨酰胺合成酶(GS)和磷酸激活谷氨酰胺酶(PAG)的表达降低,且大脑炎症标志物如白细胞介素6(IL6)、诱导型一氧化氮合酶(iNOS)和核转录因子κB(NF-κB)的表达增加(通过蛋白质免疫印迹分析),并且所研究的大脑中可溶性鸟苷酸环化酶(sGC)、胶质纤维酸性蛋白(GFAP)以及肝脏中ASS的表达下调(通过逆转录聚合酶链反应)。对高氨血症大鼠口服槲皮素(50mg/kg体重)(1)增加了尿素循环酶(CPS-1、OTC、ASS和ARG)、神经元和星形胶质细胞标志物(GS和PAG)的表达;(2)降低了IL6、iNOS和NF-κB的表达;(3)上调了SGC、GFAP和ASS的mRNA表达。我们的结果表明,槲皮素的抗高氨血症作用可能是通过其抗炎、神经保护和肝脏保护作用实现的。