Gadolinium-Based Neuroprognostic Magnetic Resonance Imaging Agents Suppress COX-2 for Prevention of Reperfusion Injury after Stroke.
Hee-Kyung KimJung-Jin LeeGaram ChoiBokyung SungYeoun-Hee KimAh Rum BaekSoyeon KimHuijin SongMinsup KimArt E ChoGang Ho LeeSungjun MoonMin-Kyoung KangJae Jun LeeYongmin ChangPublished in: Journal of medicinal chemistry (2020)
Advancements in recanalization therapies have rendered reperfusion injury an important challenge for stroke management. It is essential to work toward effective therapeutics that protect the ischemic brain from reperfusion injury. Here, we report a new concept of neuroprognostic agents, which combine molecular diagnostic imaging and targeted neuroprotection for treatment of reperfusion injury after stroke. These neuroprognostic agents are inflammation-targeted gadolinium compounds conjugated with nonsteroidal anti-inflammatory drugs (NSAIDs). Our results demonstrated that gadolinium-based MRI contrast agents conjugated with NSAIDs suppressed the increase in cyclooxygenase-2 (COX-2) levels, ameliorated glial activation, and neuron damage that are phenotypic for stroke by mitigating neuroinflammation, which prevented reperfusion injury. In addition, this study showed that the neuroprognostic agents are promising T1 molecular MRI contrast agents for detecting precise reperfusion injury locations at the molecular level. Our results build on this new concept of neuroprognostics as a novel management strategy for ischemia-reperfusion injury, combining neuroprotection and molecular diagnostics.
Keyphrases
- cerebral ischemia
- subarachnoid hemorrhage
- contrast enhanced
- magnetic resonance imaging
- brain injury
- blood brain barrier
- acute myocardial infarction
- anti inflammatory drugs
- ischemia reperfusion injury
- magnetic resonance
- computed tomography
- traumatic brain injury
- high resolution
- acute ischemic stroke
- photodynamic therapy
- heart failure
- spinal cord injury
- left ventricular
- inflammatory response
- diffusion weighted imaging
- spinal cord
- replacement therapy
- lps induced
- middle cerebral artery
- cognitive impairment