ABSTRACT
<p><b>OBJECTIVE</b>To evaluate protective effect of minocycline,a semisynthetic tetracycline derivative on different traumatic brain injuries in rats and mice.</p><p><b>METHODS</b>The opened brain trauma was induced in rats and the closed head injury and cold brain injury were induced in mice. In 3 brain trauma models, minocycline (45 mg/kg, ip) was administered twice daily for 2 d before the operation, at 30 min before and 1 h after the operation, and once daily for 2 d following the operation (totally 8 doses in 5 d). After the operation, the behavioral alteration was observed daily, lesion area and survival neuron density were measured at the end of the experiments (14 d after the injuries).</p><p><b>RESULT</b>For rat opened traumatic injury, minocycline promoted the recovery of hindlimb motor activity (inclined board angle), but did not alter other indexes. For mouse closed head traumatic injury, minocycline reduced the neuron loss, but did not improve behavioral dysfunction. For mouse cold injury-induced trauma, minocycline reduced death rate and lesion area, but did not remarkably improve behavior and neuron loss.</p><p><b>CONCLUSION</b>Minocycline only has an incomplete neuroprotective effect on different brain traumatic injuries in rats and mice.</p>
Subject(s)
Animals , Male , Mice , Rats , Brain Injuries , Drug Therapy , Mice, Inbred ICR , Minocycline , Therapeutic Uses , Neuroprotective Agents , Therapeutic Uses , Rats, Sprague-DawleyABSTRACT
<p><b>OBJECTIVE</b>To establish a new photomacrographic analysis of morphological changes on brain surface to evaluate blood-brain barrier (BBB) disruption.</p><p><b>METHODS</b>Permanent focal cerebral ischemia was induced by middle cerebral artery occlusion (MCAO) in mice. Brains were removed 10 min, 0.5, 1, 3, 6, 12 and 24 h after MCAO. The whole brains and brain slices were photographed by a digital camera. BBB disruption was evaluated by hemorrhage and traced Evans blue (EB) on the brain surface. Fluoremetric quantitation of EB and water content in the brains were also performed at various time points.</p><p><b>RESULT</b>Photomacrographic morphological analysis showed that hemorrhage and traced EB on the surface of the brains significantly increased from 3 h after focal cerebral ischemia,which were correlated to the results in the brain slices. EB content in the ischemic hemispheres was significantly increased from 0.5 h after MCAO, and water content was increased from 1 h after MCAO.</p><p><b>CONCLUSION</b>Photomacrographic measurement is a simple and useful method for evaluating BBB disruption semi-quantitatively, and can detect BBB disruption earlier after focal cerebral ischemia in mice.</p>
Subject(s)
Animals , Male , Mice , Blood-Brain Barrier , Brain , Evans Blue , Infarction, Middle Cerebral Artery , Mice, Inbred ICR , Photography , Time FactorsABSTRACT
<p><b>OBJECTIVE</b>To establish a new macrophotographic measurement of brain surface area to evaluate brain edema after focal cerebral ischemia in mice.</p><p><b>METHODS</b>Permanent focal cerebral ischemia was induced by middle cerebral artery occlusion (MCAO) in mice. The brains were removed 10,30 min,1,3,6,12 and 24 h after MCAO, and photographed in dorsal and lateral views by a digital camera. Then, 6 coronal slices of 1 mm thick were cut and photographed. Finally, the water content of brain tissue was measured by heating at 110 degrees C for 24 h. The left and right hemisphere areas of the brains and the brain slices were analyzed and calculated by MedBrain 2 imaging analyzer to evaluate brain edema.</p><p><b>RESULT</b>The macrophotographic measurement showed that the ischemic hemisphere areas significantly increased from 1 h after focal cerebral ischmia, which was similar to the measurement of water content. This measurement for brain edema correlated well with those of water content and brain slice volume.</p><p><b>CONCLUSION</b>The macrophotographic measurement is an objective and quantitative method for evaluating brain edema after focal cerebral ischemia.</p>