AI Article Synopsis

  • The study investigates the effects of whole-body vibration (WBV) from motor vehicle accidents on brain microinjury, proposing it as a potential risk factor for accidents and vascular diseases.
  • It involved 56 rats divided into groups exposed to either vibration or control conditions over periods of 2, 4, or 8 weeks, examining changes in behavior, physiology, and brain structure.
  • Findings showed that cumulative WBV led to significant brain damage, including restricted blood flow, neuron death, and chronic swelling, all correlating with brain function decline.

Article Abstract

Insidious brain microinjury from motor vehicle-induced whole-body vibration (WBV) has not yet been investigated. For a long time we have believed that WBV would cause cumulative brain microinjury and impair cerebral function, which suggests an important risk factor for motor vehicle accidents and secondary cerebral vascular diseases. Fifty-six Sprague-Dawley rats were divided into seven groups (n = 8): 1) 2-week normal control group, 2) 2-week sham control group (restrained in the tube without vibration), 3) 2-week vibration group (exposed to whole-body vibration at 30 Hz and 0.5g acceleration for 4 hr/day, 5 days/week, for 2 weeks), 4) 4-week sham control group, 5) 4-week vibration group, 6) 8-week sham control group, and 7) 8-week vibration group. At the end point, all rats were evaluated in behavior, physiological, and brain histopathological studies. The cerebral injury from WBV is a cumulative process starting with vasospasm squeezing of the endothelial cells, followed by constriction of the cerebral arteries. After the 4-week vibration, brain neuron apoptosis started. After the 8-week vibration, vacuoles increased further in the brain arteries. Brain capillary walls thickened, mean neuron size was obviously reduced, neuron necrosis became prominent, and wide-ranging chronic cerebral edema was seen. These pathological findings are strongly correlated with neural functional impairments.

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http://dx.doi.org/10.1002/jnr.23536DOI Listing

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