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Objectives: The pathogenesis of fibromyalgia syndrome (FMS) is unclear. Transcranial ultrasonography revealed anechoic alteration of midbrain raphe in depression and anxiety disorders, suggesting affection of the central serotonergic system. Here, we assessed midbrain raphe echogenicity in FMS.
Methods: Sixty-six patients underwent transcranial sonography, of whom 53 were patients with FMS (27 women, 26 men), 13 patients with major depression and physical pain (all women), and 14 healthy controls (11 women, 3 men). Raphe echogenicity was graded visually as normal or hypoechogenic, and quantified by digitized image analysis, each by investigators blinded to the clinical diagnosis.
Results: Quantitative midbrain raphe echogenicity was lower in patients with FMS compared to healthy controls (p<0.05), but not different from that of patients with depression and accompanying physical pain. Pain and FMS symptom burden did not correlate with midbrain raphe echogenicity as well as the presence and severity of depressive symptoms.
Conclusion: We found reduced echogenicity of the midbrain raphe area in patients with FMS and in patients with depression and physical pain, independent of the presence or severity of pain, FMS, and depressive symptoms. Further exploration of this sonographic finding is necessary before this objective technique may enter diagnostic algorithms in FMS and depression.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671316 | PMC |
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0277316 | PLOS |
Toxicol Res (Camb)
August 2025
Clinical Laboratory Sciences Department, Turabah University College, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Lipopolysaccharide (LPS; a bacterial endotoxin) treatment causes acute inflammatory conditions. Acute inflammation causes the brain to activate neurons in some brain nuclei known as circumventricular organs. The c-Fos immunoreaction could be used to assess this neural activity.
View Article and Find Full Text PDFBrain Res
July 2025
Graduate School of Innovative Life Science, University of Toyama, 3190 Gofuku, Toyama 930-8555, Japan; Organization for International Education and Exchange, University of Toyama, 3190 Gofuku, Toyama 930-8555, Japan. Electronic address:
The mechanisms underlying day-active behaviors in diurnal species are still unclear. We lesioned midbrain serotonergic neurons and monitored the effect on spontaneous locomotor activity in diurnal Nile grass rats. First, serotonergic neuron localization was visualized by tryptophan hydroxylase 2 immunofluorescence staining.
View Article and Find Full Text PDFNeuropharmacology
November 2025
Department of Pharmacology, University of Oxford, OX1 3QT, UK. Electronic address:
Selective serotonin reuptake inhibitor (SSRI) therapy cessation often induces a disabling discontinuation syndrome, including increased anxiety. We recently reported that SSRI discontinuation induced behavioural changes in mice, which we hypothesise arose from activated anxiety circuitry. Here, we investigated the effect of discontinuation from the SSRI paroxetine on the expression of the activity-dependent gene c-fos in selected anxiety-related midbrain and forebrain regions.
View Article and Find Full Text PDFMol Neurobiol
May 2025
School of Basic Medical Sciences, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science and Institutes of Brain Science, Huadong Hospital, Fudan University, Shanghai, China.
The parasubthalamic nucleus (PSTN) plays a crucial role in various physiological functions, including feeding, motivation, thermoregulation, exploration, sleep-wakefulness and cardiovascular system regulation. However, presynaptic partners that modulate PSTN activity are poorly understood. A significant proportion of PSTN neurons express calretinin (CR).
View Article and Find Full Text PDFInt J Neuropsychopharmacol
May 2025
Centres for Neuropsychopharmacology and Psychedelic Research, Division of Psychiatry, Department of Brain Sciences, Imperial College London, London, United Kingdom.
Background: Preclinical work suggests that chronic nicotine/tobacco use is associated with reductions in serotonin within the hippocampus, yet no research has yet shown an association of smoking behaviors and alterations in brain serotonin in humans in vivo.
Methods: We therefore analyzed existing [11C]DASB PET data from the Cimbi Database to compare the availability of the serotonin transporter (SERT) in the hippocampus, midbrain (including the raphe), and neocortex of 60 healthy non-smokers, 15 ex-smokers, and 11 current smokers who also provided blood samples for determination of plasma tryptophan load. Because SERT availability is considered to be negatively associated with extracellular serotonin levels, we hypothesized that current smokers would exhibit greater SERT availability than ex-smokers and non-smokers.