Our growth and survival depends on our adaptive ability to seek out and consume food. However, changes in eating behaviors are common to many mental disorders, whether due to changes in motivation from the illness, or as a potential side effect of its pharmacotherapy.

Of course, eating disorders (EDs) are defined by maladaptive eating. Indeed, for the millions of individuals that will battle an ED (such as anorexia nervosa, bulimia nervosa, binge-eating disorder, and avoidant restrictive food intake disorder), food-avoidance and -seeking have become debilitating and potentially life-threatening behaviors.

If we are to improve treatments and identify novel therapeutics for relapse-prone EDs (or for unwanted changes in motivation more broadly), it is absolutely critical that we understand the brain circuits, states, and signaling molecules that calibrate feeding and interpret food-related contextual cues.

The hippocampus (HPC) is critically involved in memory and the contextual regulation of motivated behaviors, which includes processing food-related cues, but how contextual signals of the HPC are integrated and processed in subcortical brain systems to scale motivated behaviors isn’t well known.

With its broad HPC afferents and robust targeting of hypothalamic networks, the highly conserved lateral septum (LS) is well-positioned to deconstruct HPC activity for regulation of context-dependent motivated behavior, including feeding. However, the LS is a heterogeneous and complex inhibitory network, whose many functions are largely unexplored…

Leveraging single-nucleus RNA sequencing, mouse genetics, cell-type-specific circuit mapping and manipulation, ex vivo slice electrophysiology, optical imaging of active cells, and rigorous behavioral testing and analyses, my ongoing postdoctoral research has identified a  unique neuropeptidergic cell-type within the HPC-LS-hypothalamus network that calibrates context-dependent eating behaviors. We are nearing submission of this work for publication (preprint soon), and I am excited to update on the specifics of these findings!

In my future lab (TBD!), I will continue to use and build on these techniques to study the HPC-LS-hypothalamus network in the adaptive control of context-dependent motivation, such as feeding. 

If any of this sounds interesting, please consider me for a talk or presentation, and please be on the lookout for my faculty application materials!

My Skills / Expertise:

Biosafety (Lvl 1/2) — Cell Culture/Mini-/Maxi-Prep/Lentivirus Preparation— Chemogenetics/DREADDs — Combinatorial Tracing of Circuits (AAV/Rabies/CTb) — ELISA — Engram Labeling/Reactivation (Fos-tTA/TRAP2/Cal-Light) — Fiber Photometry — Fluorescent/Chromogenic Immunohistochemistry (IHC) — Grantsmanship — Histology/Cryosectioning/Tissue Dissection/Fixation — In Situ Hybridization (F/ISH/RNAScope) — In Vivo Electrophysiology (Single Unit) — Intracranial Stereotactic Surgery — Intracranial/Systemic Pharmacology — Light/Fluorescent/Confocal Microscopy — Mentoring/Teaching/Pedagogy/Public Speaking — Mouse Colony Management/Genotyping/PCR — Noldus/Ethovision/Med-PC — Optogenetics/Fiber Production/Lasers — Pavlovian Fear Conditioning/Extinction/Relapse — Responsible Conduct of Research (RCR) — Rodent Handling/Animal Husbandry (Mouse/Rat/Hamster) — Statistics — Sterilization/Autoclaving — Tests for Anxiogenesis/Locomotion (OF/EPM) — Tests for Feeding/Food-Seeking (Context-Induced Overconsumption/NSF) — Tests for Social Behavior (Social Defeat/Conditioned Defeat/Social Discrimination) — Tissue Clearing/CLARITY — Tissue Quantification/ImageJ — Transcriptomics/Single-Nucleus RNA-Sequencing (snRNAseq/10X) — Valence Assays/Real-Time Place Preference (RTPP) — Western Blotting

Other Skills That I’m Currently Building / Working On:

Ex Vivo Slice Electrophysiology — In Vivo 1-P Calcium Imaging — Machine Learning of Behavior (SLEAP/DeepLabCut) — Programming (R/RStudio/Matlab)

My Published Works (Click for Links)

17) Reed L. Ressler**, Travis D. Goode**, Sohmee Kim, Karthik R. Ramanathan, Stephen Maren (2021) Covert capture and attenuation of a hippocampus-dependent memory. Nature Neuroscience 24: 677–684. PMCID: PMC8102347; Equal Contribution**

16) Travis D. Goode**, Kazumasa Z. Tanaka**, Amar Sahay, Thomas J. McHugh (2020) An integrated index: place cells, engrams and hippocampal memory. Neuron 107: 805–820. PMCID: PMC7486247; Equal Contribution**

15) Reed L. Ressler, Travis D. Goode, Carolyn Evemy, Stephen Maren (2020) NMDA receptors in the CeA and BNST differentially regulate fear conditioning to predictable and unpredictable threats. Neurobiology of Learning and Memory 174: 107281. PMCID: PMC7484222

14) Travis D. Goode, Gillian M. Acca, Stephen Maren (2020) Threat imminence dictates the role of the bed nucleus of the stria terminalis in contextual fear. Neurobiology of Learning and Memory 167: 107116. PMCID: PMC6980749

13) Travis D. Goode, Reed L. Ressler, Gillian M. Acca, Olivia Miles, Stephen Maren (2019) Bed nucleus of the stria terminalis regulates fear to unpredictable threat signals. eLife 8: e46525. PMCID: PMC6456295

12) Kelly Luyck, Travis D. Goode, Haemy Lee Masson, Laura Luyten (2019) Distinct activity patterns of the human bed nucleus of the stria terminalis and amygdala during fear learning. Neuropsychology Review 29: 181–185. PMCID: PMC6366553

11) Travis D. Goode, Stephen Maren (2018) Common neurocircuitry mediating drug and fear relapse in preclinical models. Psychopharmacology 236: 415–437. PMCID: PMC6373193

10) Roger Marek**, Jingji Jin**, Travis D. Goode**, Thomas F. Giustino, Qian Wang, Gillian M. Acca, Roopashri Holehonnur, Jonathan E. Ploski, Paul J. Fitzgerald, Timothy P. Lynagh, Joseph W. Lynch, Stephen Maren, Pankaj Sah (2018) Hippocampus-driven feed-forward inhibition of the prefrontal cortex mediates relapse of extinguished fear. Nature Neuroscience 21: 384–392. PMCID: PMC5957529; Equal Contribution**

9) Travis D. Goode, Stephen Maren (2017) Role of the bed nucleus of the stria terminalis in aversive learning and memory. Learning & Memory 24: 480–491. PMCID: PMC5580527

8) Thomas F. Giustino, Jocelyn R. Seemann, Gillian M. Acca, Travis D. Goode, Paul J. Fitzgerald, Stephen Maren (2017) β-adrenoceptor blockade in the basolateral amygdala, but not the medial prefrontal cortex, rescues the immediate extinction deficit. Neuropsychopharmacology 42: 2537–2544. PMCID: PMC5686500

7) Travis D. Goode, Crystal M. Holloway-Erickson, Stephen Maren (2017) Extinction after fear memory reactivation fails to eliminate renewal in rats. Neurobiology of Learning and Memory 142: 41–47. PMCID: PMC5457330

6) Travis D. Goode, Jingji Jin, Stephen Maren (2018) Neural circuits for fear relapse. Pp 182–202, In Neurobiology of Abnormal Emotion & Motivated Behaviors (S Sangha, D Foti, Eds) San Diego: Elsevier. PMCID: N/A

5) Brooke N. Dulka, Ellen C. Ford, Melissa A. Lee, Nathaniel J. Donnell, Travis D. Goode, Rebecca Prosser, Matthew A. Cooper (2016) Proteolytic cleavage of proBDNF into mature BDNF in the basolateral amygdala is necessary for defeat-induced social avoidance. Learning & Memory 23: 156–160. PMCID: PMC4793198

4) Travis D. Goode**, Kah-Chung Leong**, Jarid Goodman, Stephen Maren, Mark Packard (2016) Enhancement of striatum-dependent memory by conditioned fear is mediated by beta-adrenergic receptors in the basolateral amygdala. Neurobiology of Stress 3: 74–82. PMCID: PMC5146203; Equal Contribution**

3) Travis D. Goode, Janice J. Kim, Stephen Maren (2015) Reversible inactivation of the bed nucleus of the stria terminalis blocks reinstatement but not renewal of extinguished fear. eNeuro 2: ENEURO.0037-15.2015. PMCID: PMC4586936

2) Travis D. Goode, Janice J. Kim, Stephen Maren (2015) Relapse of extinguished fear after exposure to a dangerous context is mitigated by testing in a safe context. Learning & Memory 22: 170–178. PMCID: PMC4340132

1) Travis D. Goode, Stephen Maren (2014) Animal models of fear relapse. Institute for Laboratory Animal Research (ILAR) Journal 55: 246–258. PMCID: PMC4197897

(Disclaimer: I Do Not Speak For Any Employer Or Funding Agency; All Opinions My Own)