How does the brain know that orgasm is coming before orgasm begins? Masters and Johnson described sensations signaling approaching orgasm, but the neural basis of this anticipatory awareness remains unexplained.The present article terms this period Erotic Intimation. It begins at the proposed Intimation threshold, when bottom-up sexual information captures attention, and continues while orgasm feels increasingly imminent, but escalation remains redirectable. Although sexual-neuroscience studies have documented cerebellar activity before and during orgasm, they have not examined its possible predictive contribution to felt orgasmic imminence. Integrating this evidence with predictive processing, the framework proposes that cerebellar prediction interacts with salience and frontal systems as precision weighting increases the influence of bottom-up information while top-down regulation remains more influential. This account extends the interpretation of pre-orgasmic cerebellar activity beyond motor preparation to cognitive-affective anticipation. Epileptic aura provides a clinical boundary comparison, with orgasmic aura offering the closest phenomenological parallel because the feeling that orgasm is coming can arise from activity that is already ictal. The framework identifies Erotic Intimation as a distinct neuroscientific target and offers a theoretical explanation of how this anticipatory awareness may arise.
This study aimed to explore associations between social isolation, loneliness, and hypothyroidism risk, and whether genetic susceptibility modifies these links. It enrolled 434,628 hypothyroidism-free participants from the UK Biobank. Social isolation was assessed via 3 dichotomous questions, loneliness via 2 revised UCLA Loneliness Scale questions, and hypothyroidism cases via hospital/death records. Hypothyroidism polygenic risk scores (PRSs) were calculated using related genetic loci, with Cox proportional hazards models for analysis. Over a median 12.3-year follow-up, 9,873 hypothyroidism cases occurred. Demographically adjusted models showed social isolation (HR = 1.25, 95% CI 1.17-1.33) and loneliness (HR = 1.38, 95% CI 1.27-1.50) linked to higher risk. After full adjustment, only loneliness remained significant (HR = 1.12, 95% CI 1.02-1.24), while social isolation's association became insignificant. No significant interactions between loneliness/social isolation or loneliness/PRS were found. Joint analysis revealed highest risk in those with high PRS and loneliness. Findings indicate loneliness, not social isolation, is an independent hypothyroidism risk factor, regardless of genetic susceptibility and other factors.
Risk-taking behavior varies across different life domains, yet neuroimaging research has primarily focused on financial incentives, thus limiting our understanding of the neural basis for domain-specific risk-taking. This study investigates whether neural correlates of risk-taking differ between financial and social incentive domains using functional magnetic resonance imaging (fMRI). Thirty-nine participants completed an adapted Balloon Analogue Risk Task with financial (monetary rewards) and social (gifts for children) incentive conditions. Behavioral data show that participants demonstrate less risk-seeking behavior in the social compared to financial condition. Neuroimaging results revealed both domain-general and domain-specific components of risk processing. A conjunction analysis of both incentive conditions identified a common neural network across both incentive types, including bilateral striatum, dorsal anterior cingulate cortex, and left insular cortex, supporting theories of domain-general risk processing mechanisms. Contrasting both reward conditions revealed significantly stronger activation in the right inferior parietal lobule during financial compared to social risk-taking, thus indicating a neural substrate for domain-specific risk preferences. These data might bridge the gap between behavioral evidence for domain-specific risk-taking and neuroimaging research, highlighting the importance of considering the type of incentives when studying risk behavior and its neural correlates.
Smiling plays a critical role in guiding behavior during social interactions from early in human ontogeny. The current study examined whether genetic variation in the oxytocin system is linked to individual differences in medial prefrontal cortex (mPFC) responses to smiles in human infants. Results show that genetic variation in CD38 (rs3796863), linked in prior work to variation in oxytocin release, is associated with enhanced mPFC responses when 7-month-old infants were viewing smiles, but not when viewing angry or fearful faces. These findings provide novel evidence that oxytocin-related genetic variability contributes to early-emerging differences in social brain function and support the view that variability in processing of affiliative signals is influenced by neurogenetic mechanisms from early in human ontogeny.
This study examined how interpersonal neural and autonomic similarity varies when dyads shift their decision-making (DM) orientation (between cognitive and emotional orientations) while evaluating moral dilemmas with a first- and third-person perspective. Thirteen dyads participated in two interactive conditions in which they jointly negotiated moral decisions (first vs third perspective), while their electrophysiological (EEG) and autonomic activity were continuously recorded. Before each interaction, participants' DM orientations were assessed, and dyads' orientation shift was classified according to whether one or both members changed orientation between the dilemmas (single-shift vs. dual-shift dyads). Interpersonal dissimilarity was quantified through Euclidean Distance (EuDist) across EEG frequency bands and Skin Conductance Level (SCL), Heart Rate (HR), HR Variability (HRV). Delta and gamma bands showed greater inter-brain dissimilarity in frontal than temporo-central and parieto-occipital regions, indicating region-specific recruitment for moral negotiation. Regarding orientation shift, dual-shift dyads displayed significantly higher gamma-band similarity compared to single-shift dyads, regardless of moral perspective. About perspective, autonomic results revealed greater inter-individual dissimilarity during first- than third-person perspective across SCL, HR, and HRV. Current findings suggest that DM orientation shift impacts neural coherence in dyads negotiating moral dilemmas (especially gamma band), while moral dilemmas perspective influences individual autonomic engagement in dyads.
