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Published February 10, 2011 | Accepted Version
Journal Article Open

Functional identification of an aggression locus in the mouse hypothalamus


Electrical stimulation of certain hypothalamic regions in cats and rodents can elicit attack behaviour, but the exact location of relevant cells within these regions, their requirement for naturally occurring aggression and their relationship to mating circuits have not been clear. Genetic methods for neural circuit manipulation in mice provide a potentially powerful approach to this problem, but brain-stimulation-evoked aggression has never been demonstrated in this species. Here we show that optogenetic, but not electrical, stimulation of neurons in the ventromedial hypothalamus, ventrolateral subdivision (VMHvl) causes male mice to attack both females and inanimate objects, as well as males. Pharmacogenetic silencing of VMHvl reversibly inhibits inter-male aggression. Immediate early gene analysis and single unit recordings from VMHvl during social interactions reveal overlapping but distinct neuronal subpopulations involved in fighting and mating. Neurons activated during attack are inhibited during mating, suggesting a potential neural substrate for competition between these opponent social behaviours.

Additional Information

© 2011 Macmillan Publishers Limited. Received 04 July 2010. Accepted 02 December 2010. Published online 09 February 2011. We thank S. Ciocchi, S. Lin, Y. Ben-Shauland A. Wang for advice on electrode and microdrive design; M. Gerfen and M. Vondrus for microdrive fabrication; M. P. Walsh, T. D. Heitzman and V. Rush for electronics support; A. Steele, R. Robbins, S. Ossorio, K. Gunapala, A. Paul, D. Oh, C. Kim and J. Nishiguchi for behaviour annotation and video scoring; H. Kim for technical assistance; W. E. Haubensak for teaching fibre-optic implant methods; J. T. Henderson for advice on stereotactic surgery; M. Kruk for advice on electrical stimulation experiments; K. Deisseroth for the Cre-dependent ChR2–EYFP AAV construct. M. Kruk, R. Mooney and R. Simerly for comments on the manuscripts; G. Mosconi for lab management and G. Mancuso for administrative support. This work was supported in part by the Weston-Havens Foundation and Jane Coffin Childs Foundation. D.J.A. is an Investigator of the Howard Hughes Medical Institute. Author Contributions: D.L. designed, carried out and analyzed preliminary fos catFISH experiments and all other experiments, and co-wrote the manuscript; M.B. and E.L. performed additional fos catFISH experiments; P.D. and P.P. developed custom behaviour annotation software; H.L. performed some of the optogenetic experiments; D.J.A. conceived the project, suggested experiments, analysed data and co-wrote the manuscript.

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