Evidence map›Paper›PMID 39783228›Full record

ArticleImmunity, inflammation and disease2025

Isosteviol Sodium Promotes Neurological Function Recovery in a Model of Spinal Cord Injury in Rats.

Tongxia Zhang, Tao Zhang, Han Yu, Lingyi Chi

Abstract read
In one paragraph

Article in Immunity, inflammation and disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Tongxia ZhangResearch Institute of Neuromuscular and Neurodegenerative Diseases and Department of Neurology, Qilu Hospital of Shandong University, Jinan, Shandong, People's Republic of China.
Tao ZhangShandong Qidu Pharmaceutical Co. Ltd. and Shandong Provincial Key Laboratory of Neuroprotective Drugs, Zibo, Shandong, People's Republic of China.
Han YuSchool of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, People's Republic of China.
Lingyi ChiSchool of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, People's Republic of China.ORCID 0000-0002-0070-8776

Funding

This work was supported by the Promotive Research Fund for Young and Middle-Aged Scientists of Shandong Province (BS10YY026) and grants 2012TS144 and 2015TS017 from the Independent Innovation Foundation of Shandong University.
6 · The paper itself

Abstract

backgroundTraumatic spinal cord injury (SCI) is an incurable condition that is the largest cause of disability. In previous studies, Isosteviol sodium (STVNa) has been shown to protect rats against acute focal cerebral ischemia; however, the effects of STVNa on SCI recovery in rats remain unknown.

methodsSTVNa was given intraperitoneally after SCI to see if it had any neuroprotective benefits. On Days 7, 14, 21, and 28 post-SCI, functional recovery was measured using the Basso, Beattie, and Bresnahan (BBB) scoring system along with the oblique plate test. Following these evaluations, spinal cord tissues were harvested for analysis. All behavioral testing occurred between 8 a.m. and 3 p.m.

resultsWe found that STVNa improved spinal cord functional recovery in rats, as evidenced by enhanced BBB locomotor rating scale, angle of inclination, decreased cavity of spinal cord damage, and neuron death in vivo. In addition, STVNa reduced inflammation in rats following SCI, as demonstrated by a reduction in proinflammatory cytokines such as tumor necrosis factor (TNF)-α, interleukin (IL)-6, and interleukin (IL)-1β. STVNa also reduced oxidative damage in SCI rats by lowering ROS while raising SOD levels.

conclusionThese findings suggest that STVNa protects SCI rats through a variety of pathways. STVNa, in particular, may benefit the recovery of SCI by reducing oxidative stress and inflammation, leading to enhanced locomotor activity in rats with SCI.

Indexed as

Disease Models, AnimalDiterpenes, KauraneNeuroprotective AgentsRecovery of FunctionSpinal Cord InjuriesAnimalsCytokinesLocomotionMaleOxidative StressRatsRats, Sprague-DawleySpinal CordCytokinesDiterpenes, KauraneisosteviolNeuroprotective Agentsapoptosisinflammationisosteviol sodiumoxidative stressspinal cord injury

Identifiers

PMID39783228
PMCPMC11712643

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.