Biology subjects

Ikemoto, S.

Publications and source records attributed to Ikemoto, S..

7 recordsLinked to original sources

bioRxiv2026

Supramammillary projections to the lateral preoptic area drive dopamine release and active behavior

The supramammillary nucleus (SuM) is known to promote active, approach-oriented behaviors by engaging ventral tegmental area (VTA) dopamine neurons projecting to the nucleus accumbens (NAc), primarily via a glutamatergic SuM[->]medial septum (MS) pathway. However, the role of other SuM projections in this process remains unclear. Here we combined anatomical tracing, fiber photometry, chemogenetic, and optogenetic approaches to investigate the SuM[->]lateral preoptic area (LPO) pathway. We found that SuM[->]LPO neurons possess extensive collateral projections and are inhibited during consummatory behavior but activated by aversive and unexpected stimuli. Chemogenetic activation of these neurons reduced water intake and immobility during stress, while inhibition enhanced the appetitive phase for ingestive behavior and fear-related immobility. Optogenetic stimulation of SuM[->]LPO terminals reinforced behavior and elicited dopamine release in the NAc. These findings identify the SuM[->]LPO pathway as a distinct circuit that, alongside the SuM[->]MS pathway, engages mesolimbic dopamine signaling to facilitate active behavioral responses to environmental challenges.

neuroscience↗

bioRxiv2026

Parabrachial-amygdala circuit cooperates with a posterior striatal area to drive opioid withdrawal aversion

Opioid addiction treatment is often hampered by the severe dysphoria of opioid withdrawal, but withdrawal treatments are limited by incomplete understanding of brain mechanisms involved. One area frequently implicated in withdrawal symptoms is the central amygdala, whose capsular portion (CeC) is particularly strongly activated during withdrawal. Additionally, a ventral posterior striatal region that resides near CeC, the interstitial nucleus of the posterior limb of the anterior commissure (IPACc), is also activated as strikingly as CeC. However, it is still unknown how these regions are activated, nor whether their activation explains the high intensity of withdrawal dysphoria. Using RNAscope, we found that c-fos expression is induced in the parabrachial nucleus (PB), a key glutamatergic afferent of CeC, after precipitated morphine withdrawal. Chemogenetic inhibition of PB glutamatergic neurons (VG2PB) nearly eliminated withdrawal-induced CeC c-Fos, without affecting IPACc c-Fos, indicating these two nuclei are activated by distinct sources. Furthermore, VG2PB inhibition markedly reduced somatic (jumping) and modestly reduced affective (place avoidance) withdrawal behavior. On the other hand, inhibition of CeC-projecting PB neuronal subtypes expressing calcitonin gene-related peptide (CGRP) or mu opioid receptor (MOR) reduced place avoidance without affecting jumping, indicating their specific role in withdrawal aversion. Strikingly, simultaneous inhibition of VG2PB and posterior striatal region containing IPACc robustly reduced withdrawal-induced place avoidance much more than the modest effects of either inhibition alone, suggesting their cooperative action in driving aversion. Our data suggests that PB-CeC circuit and posterior striatal area constitute a cooperative system driving opioid withdrawal aversion.

neuroscience↗

bioRxiv2026

Reinforcing Nicotine Doses Activate Supramammillary VGluT2 Neurons in Mice

BackgroundAlthough nicotine reinforcement is often attributed to mesolimbic dopamine neurons in the ventral tegmental area, accumulating evidence indicates that additional brain circuits contribute to its reinforcing effects. AimsThe hypothalamic supramammillary region (SuM) has been implicated as one such substrate, yet the cellular targets and circuit mechanisms through which nicotine engages this region remain poorly understood. MethodsWe combined RNAscope in situ hybridization to identify nicotinic acetylcholine receptor (nAChR) subunits, intravenous nicotine self-administration in mice to determine doses that reliably support reinforcement, and fiber photometry to monitor calcium activity in SuM VGluT2 neurons in vivo. ResultsMice exhibited reliable nicotine self-administration across a range of doses under fixed-ratio and progressive-ratio schedules. RNAscope analysis revealed prominent expression of the {beta}2 nAChR subunit in VGluT2-expressing neurons projecting from the SuM to the medial septum. Fiber photometry recordings showed that reinforcing doses of nicotine produced rapid, infusion-locked increases in GCaMP signals in SuM VGluT2 neurons. ConclusionsThese findings identify nAChR-expressing SuM neurons as a candidate circuit substrate engaged by reinforcing doses of nicotine and extend current models of nicotine reinforcement beyond canonical mesolimbic dopamine pathways.

neuroscience↗

bioRxiv2026

Orexinergic Input to the Supramammillary Region Links Threat Salience to Approach Behavior and Dopamine Release

Orexin (hypocretin) neurons (OXN) broadcast arousal-related signals across the forebrain, yet how their inputs shape motivated behavior remains poorly understood. The supramammillary region (SuM), a posterior hypothalamic structure implicated in arousal, active coping and reward-seeking, receives dense orexin innervation. Here, we define how orexinergic terminals in the SuM (OXNSuM) integrate threat salience with approach motivational processes. Using viral tracing and RNAscope, we show that SuM neurons express both orexin receptor subtypes, with type 2 receptors predominating. Fiber photometry recordings from OXNSuM terminals reveal strong activation by footshock and conditioned threat cues, modest responses to salient sensory stimuli, and pronounced suppression during water consumption. Optogenetic stimulation of OXNSuM terminals reinforces instrumental responding, biases real-time place preference, and elicits rapid, stimulation-locked dopamine release in the nucleus accumbens. These findings identify an orexin-to-SuM pathway that is engaged by uncertainty and threat yet promotes approach behavior through coupling to mesolimbic dopamine, revealing a mechanism linking hypothalamic arousal signals to adaptive motivational responses. SIGNIFICANCE STATEMENTThe supramammillary region (SuM) has emerged as a critical node linking arousal, threat processing, and motivated behavior, yet the sources and functions of its modulatory inputs remain unclear. Here, we identify orexinergic projections to the SuM as a circuit mechanism that couples threat-related salience with approach behavior and nucleus accumbens dopamine signaling. We show that orexin terminals in the SuM are activated by stressful and uncertain stimuli but suppressed during consummatory behavior, and that selective activation of these terminals is positively reinforcing and drives rapid dopamine release. These findings reveal a pathway through which orexin neurons promote active coping and reward-seeking, advancing our understanding of how hypothalamic neuromodulation shapes mesolimbic function and adaptive behavioral responses.

neuroscience↗

bioRxiv2022

The nuclear GAPDH-HMGB cascade in cortical microglia regulates cognitive flexibility

We report a mechanism that underlies stress-induced cognitive inflexibility at the molecular level. In a mouse model under subacute stress in which deficits in rule shifting tasks were elicited, the nuclear glyceraldehyde dehydrogenase (N-GAPDH) cascade was activated specifically in microglia in the prelimbic cortex. The cognitive deficits were normalized with a pharmacological intervention with a compound (the RR compound) that selectively blocked the initiation of N-GAPDH cascade without affecting glycolytic activity. The normalization was also observed with a microglia-specific genetic intervention targeting the N-GAPDH cascade. Furthermore, hyperactivation of the prelimbic layer 5 excitatory neurons, which are known to be a neuronal substrate of cognitive inflexibility, was also normalized by the pharmacological and microglia-specific genetic interventions. The RR compound may offer a mechanism-driven, translational opportunity against stress-induced cognitive inflexibility. Taken together, we show a pivotal role of cortical microglia and microglia-neuron interaction in stress-induced cognitive inflexibility. We underscore the N-GAPDH cascade in microglia, which causally mediates stress-induced cognitive alteration.

molecular biology↗

bioRxiv2020

Medial Prefrontal Cortex Interacts with the Anteromedial Thalamus in Motivation and Dopaminergic Activity

How does the prefrontal cortex (PFC) regulate motivated behavior? Our experiments characterize the circuits of the PFC regulating motivation, reinforcement and dopamine activity, revealing a novel cortico-thalamic loop. The stimulation of medial PFC (mPFC) neurons activated many downstream regions, as shown by functional MRI. Axonal terminal stimulation of mPFC neurons in downstream regions, including the anteromedial thalamic nucleus (AM), reinforced behavior and activated midbrain dopaminergic neurons. The stimulation of AM neurons projecting to the mPFC also reinforced behavior and activated dopamine neurons, and mPFC and AM showed a positive-feedback loop organization. Reciprocal excitatory functional connectivity, as well as co-activation of the two regions, was found in human participants who watched reinforcing videos. Our results suggest that this cortico-thalamic loop regulates motivation, reinforcement and dopaminergic neuron activity.

neuroscience↗

bioRxiv2020

Supramammillary neurons projecting to the septum regulate dopamine and motivation for environmental interaction

The supramammillary region (SuM) is a posterior hypothalamic structure, known to regulate hippocampal theta oscillations and arousal. However, recent studies reported that the stimulation of SuM neurons with neuroactive chemicals, including substances of abuse, is reinforcing. We conducted experiments to illuminate how SuM neurons mediate such effects. The excitation of SuM glutamatergic (GLU) neurons was reinforcing in mice; this effect was relayed by the projections to septal GLU neurons. SuM neurons were active during exploration and approach behavior and diminished activity during sucrose consumption. Consistently, inhibition of SuM neurons disrupted approach responses, but not sucrose consumption. Such functions are similar to those of mesolimbic dopamine neurons. Indeed, the stimulation of SuM-to-septum GLU neurons and septum-to-ventral tegmental area (VTA) GLU neurons activated mesolimbic dopamine neurons. We propose that the supramammillo-septo-VTA pathway is important in reinforcement and approach motivation and may play an important role in mood and substance-use disorders.

neuroscience↗