Functional brown adipose tissue (BAT) was identified in adult humans only in 2007 with the use of fluorodeoxyglucose positron emission tomography imaging. Previous studies have demonstrated a negative correlation between obesity and BAT presence in humans. It is proposed that BAT possesses the capacity to increase metabolism and aid weight loss. In rodents it is well established that BAT is stimulated by the sympathetic nervous system with the interscapular BAT being innervated via branches of intercostal nerves. Whilst there is evidence to suggest that BAT possesses beta-3 adrenoceptors, no studies have identified the specific nerve branch that carries sympathetic innervation to BAT in humans. The aim of this study was to identify and trace the peripheral nerve or nerves that innervate human BAT in the supraclavicular region. The posterior triangle region of the neck of cadaveric specimens were dissected in order to identify any peripheral nerve branches piercing and/or terminating in supraclavicular BAT. A previously undescribed branch of the cervical plexus terminating in a supraclavicular adipose depot was identified in all specimens. This was typically an independent branch of the plexus, from the third cervical spinal nerve, but in one specimen was a branch of the supraclavicular nerve. Histological analysis revealed the supraclavicular adipose depot contained tyrosine hydroxylase immunoreactive structures, which likely represent sympathetic axons. This is the first study that identifies a nerve branch to supraclavicular BAT-like tissue. This finding opens new avenues for the investigation of neural regulation of fat metabolism in humans.

We examined the influence of linear perspective cues and texture gradients in the perceptual rescaling of stimuli over a highly-salient Ponzo illusion of a corridor. We performed two experiments using the Method of Constant Stimuli where participants judged the size of one of two rings. In experiment 1, one ring was presented in the upper visual-field at the end of the corridor and the other in the lower visual-field at the front of the corridor. The perceived size of the top and bottom rings changed as a function of the availability of linear perspective and textures. In experiment 2, only one ring was presented either at the top or the bottom of the image. The perceived size of the top but not the bottom ring changed as a function of the availability of linear perspective and textures. In both experiments, the effects of the cues were additive. Perceptual rescaling was also stronger for the top compared to the bottom ring. Additional eye-tracking revealed that participants tended to gaze more in the upper than the lower visual-field. These findings indicate that top-down mechanisms provide an important contribution to the Ponzo illusion. Nonetheless, additional maximum likelihood estimation analyses revealed that linear perspective fulfilled a greater contribution in experiment 2, which is suggestive of a bottom-up mechanism. We conclude that both top-down and bottom-up mechanisms play important roles. However, the former seems to fulfil a more prominent role when both stimuli are presented in the image.

Our objective was to determine whether the influence of linear perspective cues and texture gradients in the perceptual rescaling of stimulus size transfers from one eye to the other. In experiment 1, we systematically added linear perspective cues and texture gradients in a background image of the corridor illusion. To determine whether perceptual size rescaling takes place at earlier or later stages, we tested how the perceived size of top and bottom rings changed under binocular (rings and background presented to both eyes), monocular (rings and background presented to the dominant eye only), and dichoptic (rings and background presented separately to the dominant and nondominant eyes, respectively) viewing conditions. We found differences between viewing conditions in the perceived size of the rings when linear perspective cues, but not texture gradients, were presented. Specifically, linear perspective cues produced a stronger illusion under the monocular compared to the dichoptic viewing condition. Hence, there was partial interocular transfer from the linear perspective cues, suggesting a dominant role of monocular neural populations in mediating the corridor illusion. In experiment 2, we repeated similar procedures with a more traditional Ponzo illusion background. Contrary to findings from experiment 1, there was a full interocular transfer with the presence of the converging lines, suggesting a dominant role of binocular neural populations. We conclude that higher order visual areas, which contain binocular neural populations, are more involved in the perceptual rescaling of size evoked by linear perspective cues in the Ponzo compared to the corridor illusion.

Perineal trauma during childbirth affects millions of women worldwide every year. The aim of the Perineal Assessment and Repair Longitudinal Study (PEARLS) was to improve maternal clinical outcomes following childbirth through an enhanced cascaded multiprofessional training program to support implementation of evidence-based perineal management.

Our objective was to determine how different spatial frequencies affect the perceptual size rescaling of stimuli in the corridor illusion. Two experiments were performed using the method of constant stimuli. In experiment 1, the task required participants to compare the size of comparison and standard rings displayed over the same background image. ANOVA on the points of subject equality (PSEs) revealed that the perceived size of the top and bottom standard rings changed as a function of the availability of the high, medium, and low spatial frequency information. In experiment 2, the task required participants to compare the size of a comparison ring presented outside of the background image with a standard ring presented inside it. ANOVA on the PSEs revealed that the apparent size of the top and not the bottom standard ring changed depending on the availability of medium spatial frequency information. Eye-tracking revealed that the spatial frequency range of the background image in the periphery affected participants' eye positioning, which may explain why the effects of different spatial frequencies fluctuated across experiments. Nonetheless, when we consider these findings together, we propose that the conceptual understanding of depth plays a more important role in explaining the corridor illusion than the low-level processing of depth information extracted from different spatial frequencies along separate channels.

Pharmacological interventions to aid weight loss have historically targeted either appetite suppression or increased metabolic rate. Brown adipose tissue (BAT) possesses the capacity to expend energy in a futile cycle, thus increasing basal metabolic rate. In animal models, oestrogen has been implicated in the regulation of body weight, and it is hypothesized that oestrogen is acting by modulating BAT metabolism. A systematic search was performed, to identify research articles implementing in vivo oestrogen-related interventions and reporting outcome measures that provide direct or indirect measures of BAT metabolism. Meta-analyses were conducted where sufficient data were available. The final library of 67 articles were predominantly in rodent models and provided mostly indirect measures of BAT metabolism. Results of this review found that oestrogen's effects on body weight, in rats and possibly mice, are likely facilitated by both metabolic and appetitive mechanisms but are largely only found in ovariectomized models. There is a need for further studies to clarify the potential effects of oestrogen on BAT metabolism in gonad-intact and castrated male animal models.

The 5-hydroxytryptamine 3 (5-HT3) receptor belongs to the pentameric ligand-gated cation channel superfamily. Humans have five different 5-HT3 receptor subunits: A to E. The 5-HT3 receptors are located on the cell membrane, but a previous study suggested that mitochondria could also contain A subunits. In this article, we explored the distribution of 5-HT3 receptor subunits in intracellular and cell-free mitochondria. Organelle prediction software supported the localization of the A and E subunits on the inner membrane of the mitochondria. We transiently transfected HEK293T cells that do not natively express the 5-HT3 receptor with an epitope and fluorescent protein-tagged 5HT3A and 5HT3E subunits. Fluorescence microscopy and cell fractionation indicated that both subunits, A and E, localized to the mitochondria, while transmission electron microscopy revealed the location of the subunits on the mitochondrial inner membrane, where they could form heteromeric complexes. Cell-free mitochondria isolated from cell culture media colocalized with the fluorescent signal for A subunits. The presence of A and E subunits influenced changes in the membrane potential and mitochondrial oxygen consumption rates upon exposure to serotonin; this was inhibited by pre-treatment with ondansetron. Therefore, it is likely that the 5-HT3 receptors present on mitochondria directly impact mitochondrial function and that this may have therapeutic implications.