We had a fantastic talk today with @ZhenggangZhu on "The Dopamine Pedal"! He presented fascinating research on how our brains drive us to overeat. Thank you for the insightful presentation! #Neuroscience #Dopamine #BrainResearch
We had a fantastic talk today with @ZhenggangZhu on "The Dopamine Pedal"! He presented fascinating research on how our brains drive us to overeat. Thank you for the insightful presentation! #Neuroscience #Dopamine #BrainResearch
Flyer for SYNAPSES Symposium (Thursday October 23rd at Room 116 at 100 College Street) with talks by Ann Rose Bright, PhD at 9:00am, Peter Hasenhuetl, PhD at 10:00am, Minhyeok Chang, PhD at 11:15am, and Zhenggang Zhu, PhD at 12:15pm. Registration QR code at top right.
Join us next Thursday (10/23) for #SYNAPSES, a senior postdoc symposium @yaleneuro.bsky.social @kavliatyale.bsky.social
Talks will be given by:
- @annrosebright.bsky.social, PhDπ©βπ¬
- Peter Hasenhuetl, PhD π¬
- Minhyeok Chang, PhD π§βπ¬
- @zhenggang.bsky.social, PhD π₯Ό
Register Today! Yale only.
Weβre hiring!
My new GutβBrain Axis Lab at Northwestern is looking for a Research Technologist 2 to help build the lab and explore how the nervous system shapes gut health and disease.
π¬ Apply here: myhr.northwestern.edu/psp/hrnu/EMP...
Finally out: our recent work with Nick Betley is a view into how the brain reshapes its behavior in the face of competing survival needs- and also a potential angle on treatment targets for enduring pain.
A brief rundown...
www.nature.com/articles/s41...
Excited to share our latest paper - now out in @science.org - we showed how oxytocin modulates maternally-directed behavior in young mice (P15).
Proposal recommended for funding! Which means we have a fresh, 3-year-funded position available for a computational postdoc interested in studying dynamics of social interactions in rats, with simultaneous Neuropixels data to follow πππ
Proper job ad pending, but email me if interested!
It's officially published!! In my main postdoc work with @markplitt.bsky.social and @lgiocomo.bsky.social, we found that the hippocampus simultaneously encodes an animal's spatial position and its experience relative to reward in parallel population codes. π§΅
www.nature.com/articles/s41...
The firing of neural populations is high-dim even if their subthreshold activity is low-dim! This work by @bio-emergent.bsky.social and @haydari.bsky.social shows how, with a solvable model, a data analysis technique, and data from mouse visual cortex: www.biorxiv.org/content/10.1...
Excited to share our Science paper on HaloDA1.0-the first genetically encoded far-red dopamine sensor! π₯³It enables powerful multiplex imaging in neurons, brain slices, and live animals.π§ π¬ #GRABsensors #Dopamine www.science.org/doi/10.1126/...
Excited to share that the astrocyte-centered half of my thesis work is now out @science.org ! With @mishaahrens.bsky.social and @marcduque.bsky.social
science.org/doi/10.1126/... 1/8
Congrats, Josh and Xiaowei!
Congratulations! Well deserved!
Thrilled to share our work in ScienceAdvances: βChronic ethanol exposure produces sex-dependent impairments in value computations in the striatum.β Huge thanks to Tricia @janaklab.bsky.social, Daeyeol @ungteoriz.bsky.social, Angela, and my friend Robin!
www.science.org/doi/full/10....
Many of us use 2p scopes to image 3D volumes of brain. But then we analyze the data plane by plane, resulting in duplicated neurons, missed neurons, and low s/n. Let's go 3D!
Suite3D: Volumetric cell detection for two-photon microscopy
by @haydari.bsky.social & team.
www.biorxiv.org/content/10.1...
Congrats! Very important work!
(n/n) This work wouldnβt have been possible without the incredible efforts of the entire Sternson Lab (@BrainCaRMA, @ronggong, @vicente-rodriguez.bsky.social) and many othersβwhose contributions have been invaluable. Special thanks to @hhmi.org and @ucsdmedschool.bsky.social. Thank you for reading!
(10/n) Thanks to Dr. Dana Small for the insightful Science Perspective article on our work www.science.org/doi/10.1126/... www.science.org/doi/10.1126/...
(9/n) In short, our study shows that VTADA neurons encode food palatability at intermediate timescales, sustaining hedonic eating. Precise dopamine release timing is key for controlling the consumption phase, while GLP-1R activation during palatable food intake dampens this dopamine-driven effect
(8/n) We tested semaglutide (Ozempic), with a ramped daily dose to engage satiety pathways. Initially, it shortened feeding bouts and suppressed VTADA responses to palatable food. Yet as the dose increased, VTADA neurons reboundedβdriving overconsumption, an effect reversed by targeted inhibition
(7/n) Do VTADA neurons truly sustain hedonic eating? We boosted their activity during feeding and observed a hedonic contrast effect: laser-OFF blocks elicited a negative response, while stimulation significantly prolonged feeding bouts. Conversely, suppressing VTADA neurons reduced bout duration
(6/n) Switching from high- to low-palatability food abruptly reduces feeding and VTADA signalsβrevealing a βhedonic contrastβ effectβwhile lower-palatability food elicits shorter bout durations and negative DA responses. VTADA neurons may encode food palatability to sustain hedonic eating over time
(5/n) Prior work shows VTADA neurons respond to food cues, reward utility, and post-ingestion, yet how they encode palatability at intermediate timescales remains unclear. We found VTADA neurons remain active throughout palatable food consumption, with their activity scaling to palatability
(4/n) The VTA is diverseβits inhibitory VTAVGAT neurons can suppress VTADA cells. So how do the periLCVGLUT2 neurons fit in? We uncovered a pathway where periLCVGLUT2 neurons activate VTAVGAT neurons, which then dampen VTADA signaling to the nucleus accumbens by reducing dopamine release
(3/n) Our group discovered that the periβlocus coeruleus (periLC), downstream of hunger centers, plays a key role in promoting hedonic eating via double-negative inhibition. But how exactly does it work? Intriguingly, we identified a direct periLCβVTA pathway that selectively prolongs feeding bouts
(2/n) Hedonic eating means indulging in food for pleasure rather than necessityβthink of the βsalted-nut phenomenon.β In our study, we offered a highly palatable Ensure alongside a less tasty version and found that the tastier option led to longer feeding bouts, though not more bouts overall
(1/n) Why is it so hard to stop eating when something tastes amazing? Our new @ science.org paper reveals that dopamine helps sustain our drive for tasty treatsβand may explain how anti-obesity Ozempic tames those urges. doi.org/10.1126/science.adt0773
Congratulations!!! Truly grateful for your outstanding contribution!
New @science.org
Hedonic eating (eating for pleasure, not need) is mediated by dopamine neurons (in the brain ventral segmental area, VTA) and they are antagonized by GLP-1 drugs, such as semaglutide, leading to weight loss
www.science.org/doi/10.1126/...
Our paper from Junchol Park and collaborators that has been brewing for a while. Trying to capture our thinking about what action specification in striatum means and what would constitute evidence for such a model. Longer thread soon, but itβs online now. www.cell.com/neuron/fullt...
HCN1 channels in GABAergic amygdalar neurons underpin male-biased aggressive behaviors https://www.biorxiv.org/content/10.1101/2024.12.07.627305v1