Division of Experimental Medicine, Department of Biochemistry and Molecular Biology, George Washington University Medical Center, Washington, DC 20037, USA.
Magnes Res. 2010 Dec;23(4):S199-206. doi: 10.1684/mrh.2010.0218. Epub 2010 Oct 25.
Hypomagnesemia continues to cause difficult clinical problems, such as significant cardiac arrhythmias where intravenous magnesium therapy can be lifesaving. Nutritional deficiency of magnesium may present with some subtle symptoms such as leg cramps and occasional palpitation. We have investigated dietary-induced magnesium deficiency in rodent models to assess the pathobiology associated with prolonged hypomagnesemia. We found that neuronal sources of the neuropeptide, substance P (SP), contributed to very early prooxidant/proinflammatory changes during Mg deficiency. This neurogenic inflammation is systemic in nature, affecting blood cells, cardiovascular, intestinal, and other tissues, leading to impaired cardiac contractility similar to that seen in patients with heart failure. We have used drugs that block the release of SP from neurons and SP-receptor blockers to prevent some of these pathobiological changes; whereas, blocking SP catabolism enhances inflammation. Our findings emphasize the essential role of this cation in preventing cardiomyopathic changes and intestinal inflammation in a well-studied animal model, and also implicate the need for more appreciation of the potential clinical relevance of optimal magnesium nutrition and therapy.
低镁血症仍然会导致严重的临床问题,如严重的心律失常,此时静脉内镁治疗可能是救命的。镁的营养缺乏可能表现为一些微妙的症状,如腿部痉挛和偶尔的心悸。我们已经在啮齿动物模型中研究了饮食诱导的镁缺乏症,以评估与长期低镁血症相关的病理生物学变化。我们发现,神经肽物质 P (SP) 的神经元来源在镁缺乏期间早期就导致了促氧化剂/促炎变化。这种神经原性炎症是全身性的,影响血细胞、心血管、肠道和其他组织,导致心肌收缩力受损,类似于心力衰竭患者的情况。我们已经使用了可以阻断神经元中 SP 释放的药物和 SP 受体阻滞剂来预防这些病理生物学变化;而阻断 SP 的代谢则会增强炎症。我们的研究结果强调了这种阳离子在预防心肌病变和肠道炎症方面的重要作用,这也表明需要更多地认识到最佳镁营养和治疗的潜在临床相关性。