Researchers Sean M.J. McBride from Albert Einstein College of Medicine, Thomas A. Jongens from University of Pennsylvania School of Medicine, and their colleagues studied a mutant strain of the fruit fly Drosophila that lacks the fly version of the same gene that is mutated in humans with Fragile X syndrome. The gene, FMRP, codes for a protein that binds specific messenger RNAs--carriers of genetic information in the cell--and enables them to function properly.
The mutant flies lack the ability of normal flies to adjust courtship behavior that is dependent on learning and memory. In such conditioned courtship, a male fly learns to modify his courtship behavior--including following the female, vibrating a wing, tapping the female, and attempting to copulate--according to the response of the female.
Studies of a mouse lacking the Fragile X gene had revealed that it showed increased activity of the metabotropic glutamate receptor (mGluR) on the surface of neurons. This heightened receptor activity compromises the ability of the neurons to function properly in learning and memory. Such receptors are the receiving molecules for chemical messengers called neurotransmitters, launched from one neuron to another to trigger nerve impulses in the receiving neuron.
Reasoning that mGluR hyperactivity might underlie many of the pathologies of Fragile X syndrome, McBride and his colleagues tested whether drugs that blocked the receptor's activity might restore normal function in the mutant fly. Among these drugs was lithium, which is known to affect glutamate receptors.
They found that treatment with the drugs restored capability of the mutant flies for experience-dependent courtship behavior modification. Also, the researchers found that the restoration of this courtship behavior occurred through a reduction in mGluR activity.
"In sum, our results indicate that enhanced mGluR activity is a conserved feature of the fly model for Fragile X and is causative of some of the behavioral and neuronal phenotypes," wrote the researchers. "These findings also suggest that similar modulation of mGluR activity in Fragile X patients should be explored as an approach to ameliorate their cognitive defects and behavioral symptoms," they concluded.
Sean M.J. McBride, Catherine H. Choi, Yan Wang, David Liebelt, Evan Braunstein, David Ferreiro, Amita Sehgal, Kathleen K. Siwicki, Thomas C. Dockendorff, Hanh T. Nguyen, Thomas V. McDonald, and Thomas A. Jongens: "Pharmacological Rescue of Synaptic Plasticity, Courtship Behavior, and Mushroom Body Defects in a Drosophila Model of Fragile X Syndrome"
The researchers included Sean M.J. McBride, David Liebelt, Evan Braunstein, David Ferreiro, Hanh T. Nguyen, and Thomas V. McDonald of Albert Einstein College of Medicine; Catherine H. Choi of Drexel University College of Medicine; Yan Wang and Thomas A. Jongens of University of Pennsylvania School of Medicine; Amita Sehgal of Howard Hughes Medical Institute and University of Pennsylvania School of Medicine; Kathleen K. Siwicki of Swarthmore College; and Thomas C. Dockendorff of Miami University. The researchers thank the FRAXA Research Foundation for support of Y. Wang and partial support of S. Chiorean, as well as the gift of MPEP. This work was also supported in part by an NIH grant to T.A.J.
Publishing in Neuron, Volume 45, Number 5, March 3, 2005, pages 753–764. www.neuron.org
Journal
Neuron