Chakraborty Saikat, Yadav Sudhir K, Subramanian Mahesh, Iwaoka Michio, Chattopadhyay Subrata
Bio-Organic Division, Bhabha Atomic Research Centre, Mumbai 400 085, India.
Department of Chemistry School of Science, Tokai University, Kitakaname, Hiratsuka-shi, Kanagawa 259-1292, Japan.
Biochim Biophys Acta. 2014 Dec;1840(12):3385-92. doi: 10.1016/j.bbagen.2014.09.004. Epub 2014 Sep 16.
The importance of the arginine metabolism in gastric ulcer-healing is given relatively less attention. Hence the role of controlling this pathway by dl-trans-3,4-dihydroxy-1-selenolane (DHSred) and omeprazole against indomethacin-induced stomach ulceration in mouse was investigated.
Swiss albino mice were ulcerated with indomethacin followed by treatment with the test samples, and the activities of myeloperoxidase (MPO), total nitric oxide synthase (NOS) and arginase, the expressions of inducible nitric oxide synthase (iNOS) and endothelial nitric oxide synthase (eNOS), and the pro-/anti-inflammatory cytokine levels were assayed. NOS-inhibitors were also used to establish the biochemical mechanism.
Indomethacin induced maximum ulceration in mice on the 3rd day, associated with reduced arginase activity, eNOS expression, along with increased MPO and total NOS activities, nitric oxide (NO) generation, iNOS expression, and pro-/anti-inflammatory (Th1/Th2) cytokine ratio. Treatment with DHSred (2.5mgkg(-1)×3days) restored the cytokine balance to shift the iNOS/NO axis to the arginase/polyamine axis as revealed from the increased arginase activity and eNOS expression, and reduced iNOS expression, total NOS activity and NO level.
The ulcer-healing property of DHSred, but not of omeprazole was due to a favorable pro-/anti-inflammatory cytokine ratio that shifted the arginine metabolism to the polyamine pathway and increased the eNOS/iNOS ratio. The healing action of omeprazole was not significantly associated with these parameters.
The shift in the ariginine-metabolism from the iNOS/NO axis to the arginase/polyamine axis is guided by Th1/Th2 cytokines ratio and plays an important role in gastric ulcer-healing. The favourable effects of the non-toxic and water-soluble compound, DHSred on these pathways and other COX-dependent and antioxidative parameters suggested it to be a promising anti-ulcer formulation for further studies.
精氨酸代谢在胃溃疡愈合中的重要性相对较少受到关注。因此,研究了dl-反式-3,4-二羟基-1-硒戊环(DHSred)和奥美拉唑通过控制该途径对吲哚美辛诱导的小鼠胃溃疡的作用。
用吲哚美辛使瑞士白化小鼠发生溃疡,然后用测试样品进行治疗,并检测髓过氧化物酶(MPO)、总一氧化氮合酶(NOS)和精氨酸酶的活性、诱导型一氧化氮合酶(iNOS)和内皮型一氧化氮合酶(eNOS)的表达以及促炎/抗炎细胞因子水平。还使用NOS抑制剂来确定生化机制。
吲哚美辛在第3天诱导小鼠出现最大程度的溃疡,同时精氨酸酶活性降低、eNOS表达降低,以及MPO和总NOS活性增加、一氧化氮(NO)生成增加、iNOS表达增加和促炎/抗炎(Th1/Th2)细胞因子比值增加。DHSred(2.5mgkg(-1)×3天)治疗可恢复细胞因子平衡,使iNOS/NO轴转向精氨酸酶/多胺轴,这从精氨酸酶活性增加和eNOS表达增加以及iNOS表达降低、总NOS活性和NO水平降低可以看出。
DHSred而非奥美拉唑的溃疡愈合特性归因于有利的促炎/抗炎细胞因子比值,该比值使精氨酸代谢转向多胺途径并增加了eNOS/iNOS比值。奥美拉唑的愈合作用与这些参数无显著关联。
精氨酸代谢从iNOS/NO轴转向精氨酸酶/多胺轴受Th1/Th2细胞因子比值引导,并在胃溃疡愈合中起重要作用。无毒且水溶性的化合物DHSred对这些途径以及其他COX依赖性和抗氧化参数的有利影响表明它是一种有前途的抗溃疡制剂,值得进一步研究。