What does neuroimaging reveal about different penile regions (glans, frenulum, shaft) and subjective pleasure?

Checked on January 28, 2026
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Executive summary

Neuroimaging studies show that tactile stimulation of different penile regions—especially the frenulum and penile shaft—engages both classical somatosensory areas and broader affective/visceral networks, and that subjective pleasure does not map one-to-one onto a single brain locus; instead, the frenulum produces the strongest pleasure reports and distinct network effects, while the shaft shows patterns consistent with affective touch processing via secondary somatosensory cortex (S2) and thalamic input [1] [2] [3].

1. The mapping: classical somatosensory cortex and beyond

Functional imaging consistently finds that genital stimulation activates the canonical somatosensory matrix (primary and secondary somatosensory cortices) but also recruits limbic, insular, and subcortical regions implicated in visceral sensation and autonomic control—findings summarized in reviews of human sexual neuroimaging [4] [5] [6].

2. Frenulum: subjective pleasure peaks and default‑mode suppression

Psychophysical–fMRI work reports that frenulum stimulation produced the highest subjective pleasure ratings among tested penile sites and was associated with the greatest deactivation of the brain’s default‑mode network, suggesting a shift of attention/engagement rather than a simple increase in primary somatosensory signal [1] [2].

3. Penile shaft: CT‑like affective touch signature and S2 involvement

The penile shaft appears to contain C‑fibers responsive to pleasant, affective touch and, in imaging contrasts, triggered stronger S2 responses for CT‑targeted (affective) stimulation than other conditions; this implicates S2 in distinguishing affective versus discriminative touch on the shaft, consistent with affective touch findings in hairy skin [2] [7] [1].

4. Thalamus and deeper relay differences by subregion

Ultra‑high‑field (7T) fMRI of passive, non‑arousing tactile stimulation localized shaft-related activation to posterior thalamic territories (VPL) and showed that subcortical responses differ by site, indicating that ascending pathways to cortex can vary with which penile region is stimulated [3].

5. Insula, hypothalamus and the subjective‑arousal interface

Imaging literature emphasizes the posterior insula’s role in processing genital input and the hypothalamus’ role in generating erections and autonomic sexual responses; together these regions help translate somatosensory input into visceral awareness and arousal, so subjective pleasure reflects integration across somatosensory, insular, limbic and hypothalamic nodes rather than a single “pleasure center” [4] [8] [6].

6. Methodological caveats that shape conclusions

Most human genital imaging studies use small samples, non‑arousing or partner‑mediated stimulation, and varying field strengths and analyses, which limit spatial sensitivity and generalizability; the psychophysical/fMRI study that finds frenulum > shaft effects had ~19 volunteers and noted task design influences on pleasure ratings, underscoring that effect sizes are small and results can hinge on stimuli and analysis choices [2] [7] [1].

7. How subjective pleasure maps to brain activity—an integrated, networked view

Taken together, the data argue that subjective pleasure from different penile regions is better understood as differences in how peripheral afferents (including CT‑like C‑fibers on the shaft and dense mechanoreception at the frenulum) drive distinct patterns of cortical, insular and subcortical network activity—frenulum stimulation producing the largest subjective hedonic response and default‑mode suppression, shaft stimulation engaging affective‑touch processing in S2 and thalamic relays—while broader sexual arousal circuits (hypothalamus, limbic regions) modulate the overall experience [1] [2] [3] [4].

Want to dive deeper?
How do C‑tactile afferents differ across genital and non‑genital skin, and what does that imply for affective touch processing?
What are the limitations of fMRI and PET in studying sexual arousal and how have 7T studies changed anatomical specificity?
How do subjective reports of genital pleasure correlate with measures of autonomic arousal (erection) and neural activation across studies?