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N'-[(2,4-二羟基苯基)亚甲基]-2-(3,4-二甲基-5,5-二氧代吡唑并[4,3-c][1,2]苯并噻嗪-1(4H)-基)乙酰肼的抗关节炎活性

Anti-arthritic activity of N'-[(2,4-dihydroxyphenyl)methylidene]-2-(3,4-dimethyl-5,5-dioxidopyrazolo[4,3-c][1,2]benzothiazin-1(4H)-yl)acetohydrazide.

作者信息

Shabbir Arham, Shahzad Muhammad, Ali Akbar, Zia-ur-Rehman Muhammad

机构信息

Department of Pharmacology, University of Health Sciences, Lahore, Pakistan; Department of Pharmacy, COMSATS Institute of Information Technology, Abbottabad 22060, Pakistan.

Department of Pharmacology, University of Health Sciences, Lahore, Pakistan.

出版信息

Eur J Pharmacol. 2014 Sep 5;738:263-72. doi: 10.1016/j.ejphar.2014.05.045. Epub 2014 Jun 2.

Abstract

Benzothiazine and pyrazole derivatives possess anti-inflammatory properties. Previously, synergism of both heterocyclic moieties into a single nucleus has shown to produce biologically active N'-arylmethylidene-2-(3,4-dimethyl-5,5-dioxidopyrazolo(4,3-c)(1,2)benzothiazin-2(4H)yl)acetohydrazides) compound. Present study investigates the anti-arthritic effect and possible mechanism of 2,4-dihydroxyphenyl derivative (DHP) in Freund's complete adjuvant-induced arthritic rat model. Ankle joint histopathology was performed with Hematoxylin & Eosin staining, while serum C-reactive protein (CRP) levels were measured by agglutination method. mRNA expression levels and protein levels of proinflammatory markers were measured by real time reverse transcription polymerase chain reaction and Enzyme linked immunosorbent assay (ELISA), respectively. in vitro Concanavalin A (ConA)-stimulated splenocyte proliferation was also measured by ELISA reader. DHP treatment reduced the macroscopic arthritic score, CRP levels, synovial inflammation, bone erosion and pannus formation. Levels of cyclooxygenase-1 (COX-1), cyclooxygenase-2 (COX-2), Prostaglandin-E2 (PGE2), and 5-lipoxygenase (5-LOX), were significantly attenuated by DHP. It also significantly decreased the levels of toll-like receptor 2, nuclear factor-kappaB (NF-ĸB), and tissue necrosis factor-α (TNF-α) and non-significantly elevated interleukin-4 (IL-4) levels. Piroxicam, used as reference drug, significantly reduced the levels of COX-1, COX-2, PGE2, NF-ĸB, and TNF-α, but did not show reduction in 5-LOX and toll-like receptor 2 levels. However piroxicam significantly enhanced the levels of IL-4. Both DHP and piroxicam suppressed ConA-stimulated splenocyte proliferation. DHP normalized all altered hematological markers and did not show any sign of hepatotoxicity or nephrotoxicity as determined by alanine transaminase, aspartate aminotransferase, urea, and creatinine levels. Results showed that DHP possesses significant anti-arthritic activity which may be attributed to its immunomodulatory and anti-inflammatory effects.

摘要

苯并噻嗪和吡唑衍生物具有抗炎特性。此前,将这两个杂环部分整合到一个单环中已显示可产生具有生物活性的N'-芳基亚甲基-2-(3,4-二甲基-5,5-二氧代吡唑并(4,3-c)(1,2)苯并噻嗪-2(4H)基)乙酰肼化合物。本研究调查了2,4-二羟基苯基衍生物(DHP)在弗氏完全佐剂诱导的关节炎大鼠模型中的抗关节炎作用及可能机制。用苏木精和伊红染色进行踝关节组织病理学检查,同时通过凝集法测定血清C反应蛋白(CRP)水平。分别通过实时逆转录聚合酶链反应和酶联免疫吸附测定(ELISA)测量促炎标志物的mRNA表达水平和蛋白质水平。体外还通过酶标仪测量刀豆蛋白A(ConA)刺激的脾细胞增殖。DHP治疗降低了宏观关节炎评分、CRP水平、滑膜炎症、骨侵蚀和血管翳形成。DHP显著降低了环氧化酶-1(COX-1)、环氧化酶-2(COX-2)、前列腺素-E2(PGE2)和5-脂氧合酶(5-LOX)的水平。它还显著降低了Toll样受体2、核因子-κB(NF-κB)和组织坏死因子-α(TNF-α)的水平,并且非显著地提高了白细胞介素-4(IL-4)的水平。用作参考药物的吡罗昔康显著降低了COX-1、COX-2、PGE2、NF-κB和TNF-α的水平,但未显示5-LOX和Toll样受体2水平降低。然而,吡罗昔康显著提高了IL-4的水平。DHP和吡罗昔康均抑制ConA刺激的脾细胞增殖。DHP使所有改变的血液学标志物恢复正常,并且根据丙氨酸转氨酶、天冬氨酸转氨酶、尿素和肌酐水平测定未显示任何肝毒性或肾毒性迹象。结果表明,DHP具有显著的抗关节炎活性,这可能归因于其免疫调节和抗炎作用。

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