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Mohammad Akhter Hossain

Researcher at Florey Institute of Neuroscience and Mental Health

Publications -  9
Citations -  226

Mohammad Akhter Hossain is an academic researcher from Florey Institute of Neuroscience and Mental Health. The author has contributed to research in topics: Relaxin-3 & Neuropeptide. The author has an hindex of 6, co-authored 9 publications receiving 166 citations. Previous affiliations of Mohammad Akhter Hossain include University of Melbourne.

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Minimization of human relaxin-3 leading to high-affinity analogues with increased selectivity for relaxin-family peptide 3 receptor (RXFP3) over RXFP1.

TL;DR: These novel RXFP3-selective peptides represent valuable pharmacological tools to study the physiological roles of H3 relaxin/RXFP3 systems in the brain and important leads for the development of novel compounds for the treatment of affective and cognitive disorders.
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Central injection of relaxin-3 receptor (RXFP3) antagonist peptides reduces motivated food seeking and consumption in C57BL/6J mice

TL;DR: Existing anatomical and functional evidence suggests the highly-conserved neuropeptide, relaxin-3, which signals via its cognate Gi/o-protein coupled receptor, RXFP3, contributes to behavioural arousal and feeding behaviour in rodents, and in light of the established biological and translational importance of other arousal systems, relax in-3/RXFP3 networks warrant further experimental investigation.
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Central relaxin-3 receptor (RXFP3) activation reduces elevated, but not basal, anxiety-like behaviour in C57BL/6J mice

TL;DR: Overall, data suggest exogenous RXFP3 agonists can reduce elevated (FG-7142-induced) levels of anxiety in mice; data important for gauging how conserved such effects are, with a view to modelling human pathophysiology and the likely therapeutic potential of RX FP3-targeted drugs.
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RLN3/RXFP3 Signaling in the PVN Inhibits Magnocellular Neurons via M-like Current Activation and Contributes to Binge Eating Behavior.

TL;DR: It is demonstrated that relaxin-3/RXFP3 signaling in the hypothalamic paraventricular nucleus (PVN) is necessary for the expression of binge-eating behavior in female rats and identified RXFP3 as a therapeutic target for binge-like eating disorders.