α-melanocyte stimulating hormone suppresses intracerebral tumor necrosis factor-α and interleukin-1β gene expression following transient cerebral ischemia in mice
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Acknowledgements
Supported by NIH MH44694 and a New England Medical Center Research Grant.
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Multiple beneficial effects of melanocortin MC<inf>4</inf> receptor agonists in experimental neurodegenerative disorders: Therapeutic perspectives
2017, Progress in NeurobiologyCitation Excerpt :Neuroprotective properties of melanocortin agonists have been demonstrated in several models of brain ischemia (Table 2). α-MSH administration improved the recovery of auditory-evoked potentials in a dog model of transient brain stem ischemia (Huh et al., 1997) and reduced brain inflammation in transient global and focal cerebral ischemia in mice (Huang and Tatro, 2002). Recently, we provided the first evidence that short-term treatment (up to 11 days) with nanomolar amounts of [Nle4,D-Phe7]α-MSH (NDP-α-MSH) and its analog RO27-3225 induce a strong neuroprotection against damage consequent to global or focal cerebral ischemia in gerbils and rats.
Melanocortin MC4 receptor agonists alleviate brain damage in abdominal compartment syndrome in the rat
2015, NeuropeptidesCitation Excerpt :Hemorrhagic shock, traumatic brain injury or sepsis will each increase these types of brain damage caused by IAH. MC is generally believed to inhibit brain inflammation, protect neurons and restore cognition in cerebral ischemia and reperfusion (Giuliani et al., 2006b; Huang and Tatro, 2002; Spaccapelo et al., 2011; Tatro, 2006). However, due to the abrupt onset and rapid disease progression of IAH, we focused on the protective role of MC on the brain within the short-term in this study.
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