Comparative Evaluation of Neuroprotective Activity of Tryptanthrin and Its Oxime in Middle Cerebral Artery Occlusion in Rats

The neuroprotective activity of tryptanthrin and its oxime was compared in male Wistar rats with a model of intraluminal occlusion of the middle cerebral artery. Neurobehavioral tests were performed 4, 24, and 48 h after focal cerebral infarction (FCI) using a modified neurological severity score (m...

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Veröffentlicht in:Bulletin of experimental biology and medicine 2024-07, Vol.177 (3), p.344-348
Hauptverfasser: Chernysheva, G. A., Smolyakova, V. I., Plotnikov, M. B., Ulyakhina, O. A., Osipenko, A. N., Kovrizhina, A. R., Khlebnikov, A. I.
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container_start_page 344
container_title Bulletin of experimental biology and medicine
container_volume 177
creator Chernysheva, G. A.
Smolyakova, V. I.
Plotnikov, M. B.
Ulyakhina, O. A.
Osipenko, A. N.
Kovrizhina, A. R.
Khlebnikov, A. I.
description The neuroprotective activity of tryptanthrin and its oxime was compared in male Wistar rats with a model of intraluminal occlusion of the middle cerebral artery. Neurobehavioral tests were performed 4, 24, and 48 h after focal cerebral infarction (FCI) using a modified neurological severity score (mNSS); additionally, the horizontal stability test, the plantar sensitivity test of the fore and hind limbs, holding on the tilted cage top test, and negative geotaxis test were performed. The size of FCI and the severity of brain tissue swelling were examined on day 2 after occlusion. Tryptanthrin and its oxime were administered at a dose of 10 mg/kg intraperitoneally during FCI, then daily for 2 days. In the control group, the mean score of neurological deficit remained at a high level for 2 days. FCI size was 43.8±3.4% of hemisphere area, and the hemisphere volume increased by 18.5±2.0% due to brain tissue swelling and edema. Administration of tryptanthrin and its oxime significantly decreased neurological deficits at all control points and reduced FCI size (by 24.2 and 30.4%, respectively) and brain tissue swelling of the affected hemisphere (by 64.9 and 62.7%, respectively). Therefore, the neuroprotective effect of tryptanthrine and its oxime in the acute period of FCI is largely determined by their anti-inflammatory activity.
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R.</au><au>Khlebnikov, A. I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative Evaluation of Neuroprotective Activity of Tryptanthrin and Its Oxime in Middle Cerebral Artery Occlusion in Rats</atitle><jtitle>Bulletin of experimental biology and medicine</jtitle><stitle>Bull Exp Biol Med</stitle><addtitle>Bull Exp Biol Med</addtitle><date>2024-07-01</date><risdate>2024</risdate><volume>177</volume><issue>3</issue><spage>344</spage><epage>348</epage><pages>344-348</pages><issn>0007-4888</issn><issn>1573-8221</issn><eissn>1573-8221</eissn><abstract>The neuroprotective activity of tryptanthrin and its oxime was compared in male Wistar rats with a model of intraluminal occlusion of the middle cerebral artery. Neurobehavioral tests were performed 4, 24, and 48 h after focal cerebral infarction (FCI) using a modified neurological severity score (mNSS); additionally, the horizontal stability test, the plantar sensitivity test of the fore and hind limbs, holding on the tilted cage top test, and negative geotaxis test were performed. The size of FCI and the severity of brain tissue swelling were examined on day 2 after occlusion. Tryptanthrin and its oxime were administered at a dose of 10 mg/kg intraperitoneally during FCI, then daily for 2 days. In the control group, the mean score of neurological deficit remained at a high level for 2 days. FCI size was 43.8±3.4% of hemisphere area, and the hemisphere volume increased by 18.5±2.0% due to brain tissue swelling and edema. Administration of tryptanthrin and its oxime significantly decreased neurological deficits at all control points and reduced FCI size (by 24.2 and 30.4%, respectively) and brain tissue swelling of the affected hemisphere (by 64.9 and 62.7%, respectively). Therefore, the neuroprotective effect of tryptanthrine and its oxime in the acute period of FCI is largely determined by their anti-inflammatory activity.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>39126546</pmid><doi>10.1007/s10517-024-06186-w</doi><tpages>5</tpages></addata></record>
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subjects Animal models
Animals
Anti-inflammatory agents
Biomedical and Life Sciences
Biomedicine
Brain - drug effects
Brain - pathology
Brain Edema - drug therapy
Brain Edema - pathology
Brain research
Carotid arteries
Cell Biology
Cerebral blood flow
Cerebral infarction
Disease Models, Animal
Drug dosages
Edema
Geotaxis
Infarction, Middle Cerebral Artery - drug therapy
Infarction, Middle Cerebral Artery - pathology
Internal Medicine
Ischemia
Laboratory Medicine
Limbs
Male
Medical research
Neurological diseases
Neuroprotection
Neuroprotective Agents - pharmacology
Neuroprotective Agents - therapeutic use
Oximes - pharmacology
Oximes - therapeutic use
Pathology
Pharmacology
Quinazolines - pharmacology
Quinazolines - therapeutic use
Rats
Rats, Wistar
Regenerative medicine
Sensitivity analysis
Stroke
Veins & arteries
title Comparative Evaluation of Neuroprotective Activity of Tryptanthrin and Its Oxime in Middle Cerebral Artery Occlusion in Rats
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