Hemispheric specialization or asymmetry in higher brain functions such as language is well accepted. This study was designed to quantitatively determine if the hemispheric asymmetry is measurable in the somatosensory system. Twenty-two participants were studied with magnetoencephalography (MEG) while their left and right index fingers were stimulated in randomized order. The finger representation in the cortex was volumetrically localized using a wavelet based beamformer. The strength of functional activity was estimated with an intensity volume while the waveforms of the virtual sensors were computed with a virtual sensor placed in the center of localized finger area. The results showed that the latency of the first identifiable response evoked by left finger stimulation was significantly shorter than that evoked by right finger stimulation (p<0.05). The left somatosensory cortex generated higher frequency neuromagnetic signals than did the right somatosensory cortex (p<0.05). Moreover, the volume of neuromagnetic activation elicited by right finger stimulation was significantly larger than that elicited by left finger stimulation in males (p<0.001). The neuromagnetic activation revealed by virtual sensors was more consistent than that revealed by physical sensors across participants. We conclude that neuromagnetic activities in the left and right somatosensory cortices have significant differences in terms of response latency, oscillation frequency and activation volume in high-frequency neuromagnetic signals. An investigation of the hemispheric specific features of neuromagnetic activation in the somatosensory cortex lays a foundation for the study of psychophysiologic asymmetries in the brain.
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http://dx.doi.org/10.1016/j.ijpsycho.2008.10.009 | DOI Listing |
iScience
December 2024
Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang 110004, P.R. China.
Preeclampsia (PE) is a multifactorial disorder of pregnancy, characterized by new-onset gestational hypertension. High-throughput mRNA sequencing (RNA-seq) was performed to analyze the gene expression patterns in placentas from patients with early-onset PE (EOPE). PR domain zinc-finger protein 1 (PRDM1) expression increased in the chorionic villi and placental basal plate from patients with PE and nitro--arginine methyl ester (L-NAME)-treated rats.
View Article and Find Full Text PDFPLoS One
January 2025
Department of Orthopedics, Shanghai Pudong New Area People's Hospital, Shanghai, China.
J Med Food
December 2024
Division of Food and Nutrition and Human Ecology Research Institute, Chonnam National University, Gwangju, Republic of Korea.
Here, we investigated whether a mixture of and (1:3, KGC01CE) could suppress muscle atrophy in HO-induced C2C12 cells and dexamethasone-injected mice. Our results revealed that KGC01CE effectively safeguarded against HO-induced muscle atrophy in C2C12 cells compared with the same mixture at other ratios. We demonstrated that dexamethasone elicited oxidative stress in muscle tissue and decreased the grip strength and cross-sectional areas of muscle fibers; however, oral administration of KGC01CE (1:3) suppressed these dexamethasone-induced changes.
View Article and Find Full Text PDFMar Drugs
December 2024
Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Republic of Korea.
The objective of this study was to examine whether fucosterol, a phytosterol of marine algae, could ameliorate skeletal muscle atrophy in tumor necrosis factor-alpha (TNF-α)-treated C2C12 myotubes and in immobilization-induced C57BL/6J mice. Male C57BL6J mice were immobilized for 1 week to induce skeletal muscle atrophy. Following immobilization, the mice were administrated orally with saline or fucosterol (10 or 30 mg/kg/day) for 1 week.
View Article and Find Full Text PDFInt Immunopharmacol
December 2024
School of Pharmacy, Nantong University, Nantong, Jiangsu, China. Electronic address:
Non-alcoholic steatohepatitis (NASH) is the most common cause of chronic liver diseases with its pathophysiological mechanism poorly understood. In this work, serological, histological, molecular biological, biochemical, and immunological methods were applied to explore the pathological significance and action of zinc finger protein 281 (ZFP281 in mouse, ZNF281 in human) and targeted strategies. We reported that ZFP281/ZNF281 abundance in hepatocytes was positively correlated with the progression of NASH.
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