Highlights d Thyroid hormone induces browning independent of sympathetic nervous system through TRb d Despite high UCP1, the beige fat lacks adrenergic input and is inactive d Thyroid hormone's metabolic and thermogenic effects are maintained in UCP1 knockout mice d Thyroid hormone induces hyperthermia and elevates the body temperature setpoint

Highlights d GLP-1 inhibits glucose uptake and promotes b-oxidation in cultured astrocytes d Lack of astrocyte GLP-1R in vivo activates a stress response and increases FGF21 d Adaptations to astrocyte GLP-1R deletion improve glucose metabolism and memory

Highlights d Acute high-fat-diet feeding activates PNOC neurons in the arcuate nucleus (ARC) d GABAergic PNOC ARC neurons inhibit anorexigenic POMC neurons d Optogenetic activation of PNOC ARC neurons promotes feeding d Ablation of PNOC ARC neurons protects from obesity

Highlights d Food intake induces orosensory and post-ingestive dopamine release in humans d Both recruit distinct pathways: orosensory integrative and higher cognitive centers d Dopamine release in ''wanting''-associated regions mirrors subjective desire to eat d Post-ingestive dopamine release in the putamen is inversely correlated to ''wanting''

Highlights d Intersectional mapping of sensory neurons identifies distinct gut innervation patterns d Gut-innervating GLP1R+ vagal afferents relay anorexigenic signals to brainstem neurons d Gut-innervating GPR65+ vagal afferent stimulation increases hepatic glucose production d GLP1R+ vagal afferent activity is required to control glycemia during feeding

It has been suggested that there are two distinct and parallel mechanisms for controlling instrumental behavior in mammals: goal-directed actions and habits. To gain an understanding of how these two systems interact to control behavior, it is essential to characterize the mechanisms by which the balance between these systems is influenced by experience. Studies in rodents have shown that the amount of training governs the relative expression of these two systems: Behavior is goal-directed following moderate training, but the more extensively an instrumental action is trained, the more it becomes habitual. It is less clear whether humans exhibit similar training effects on the expression of goal-directed and habitual behavior, as human studies have reported contradictory findings. To tackle these contradictory findings, we formed a consortium, where four laboratories undertook a preregistered experimental induction of habits by manipulating the amount of training. There was no statistical evidence for a main effect of the amount of training on the formation and expression of habits. However, exploratory analyses suggest a moderating effect of the affective component of stress on the impact of training over habit expression. Participants who were lower in affective stress appeared to be initially goal-directed, but became habitual with increased training, whereas participants who were high in affective stress were already habitual even after moderate training, thereby manifesting insensitivity to overtraining effects. Our findings highlight the importance of the role of moderating variables such as individual differences in stress and anxiety when studying the experimental induction of habits in humans.

To date, the spatiotemporal release of specific neurotransmitters at physiological levels in the human brain cannot be detected. Here, we present a method that relates minute-by-minute fluctuations of the positron emission tomography (PET) radioligand [11C]raclopride directly to subsecond dopamine release events. We show theoretically that synaptic dopamine release induces low frequency temporal variations of extrasynaptic extracellular dopamine levels, at time scales of one minute, that can evoke detectable temporal variations in the [11C]raclopride signal. Hence, dopaminergic activity can be monitored via temporal fluctuations in the [11C]raclopride PET signal. We validate this theory using fast-scan cyclic voltammetry and [11C]raclopride PET in mice during chemogenetic activation of dopaminergic neurons. We then apply the method to data from human subjects given a palatable milkshake and discover immediate and—for the first time—delayed food-induced dopamine release. This method enables time-dependent regional monitoring of stimulus-evoked dopamine release at physiological levels.

In this work, we illustrate a method to continuously hyperpolarize a biomolecule, nicotinamide, in water using parahydrogen and signal amplification by reversible exchange (SABRE). Building on the preparation procedure described recently by Truong et al. [ J. Phys. Chem. B , 2014 , 118 , 13882 - 13889 ], aqueous solutions of nicotinamide and an Ir-IMes catalyst were prepared for low-field NMR and MRI. The (1)H-polarization was continuously renewed and monitored by NMR experiments at 5.9 mT for more than 1000 s. The polarization achieved corresponds to that induced by a 46 T magnet (P = 1.6 × 10(-4)) or an enhancement of 10(4). The polarization persisted, although reduced, if cell culture medium (DPBS with Ca(2+) and Mg(2+)) or human cells (HL-60) were added, but was no longer observable after the addition of human blood. Using a portable MRI unit, fast (1)H-MRI was enabled by cycling the magnetic field between 5 mT and the Earth's field for hyperpolarization and imaging, respectively. A model describing the underlying spin physics was developed that revealed a polarization pattern depending on both contact time and magnetic field. Furthermore, the model predicts an opposite phase of the dihydrogen and substrate signal after one exchange, which is likely to result in the cancelation of some signal at low field.