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Details

Autor(en) / Beteiligte
Titel
Tanshinone IIA attenuates the inflammatory response and apoptosis after traumatic injury of the spinal cord in adult rats
Ist Teil von
  • PloS one, 2012-06, Vol.7 (6), p.e38381-e38381
Ort / Verlag
United States: Public Library of Science
Erscheinungsjahr
2012
Quelle
MEDLINE
Beschreibungen/Notizen
  • Spinal cord injury (SCI), including immediate mechanical injury and secondary injury, is associated with the inflammatory response, apoptosis and oxidative stress in response to traumatic injury. Tanshinone IIA (TIIA) is one of the major extracts obtained from Salvia miltiorrhiza BUNGE, which has anti-inflammatory and anti-apoptotic effects on many diseases. However, little is known about the effects of TIIA treatment on SCI. Therefore, the aim of the present study is to evaluate the pharmacological action of TIIA on secondary damage and the underlying mechanisms of experimental SCI in rats. SCI was generated using a weight drop device on the dorsal spinal cord via a two-level T9-T11 laminectomy. SCI in rats resulted in severe trauma, characterized by locomotor disturbance, edema, neutrophil infiltration, the production of astrocytes and inflammatory mediators, apoptosis and oxidative stress. TIIA treatment (20 mg/kg, i.p.) after SCI induced significant effects: (1) improved motor function (Basso, Beattie and Bresnahan scores), (2) reduced the degree of tissue injury (histological score), neutrophil infiltration (myeloperoxidase activity) and the expression of astrocytes, (3) inhibited the activation of SCI-related pathways, such as NF-κB and MAPK signaling pathways, (4) decreased the production of pro-inflammatory cytokines (TNF-α, IL-1β, and IL-6) and iNOS, (5) reduced apoptosis (TUNEL staining, and Bcl-2 and caspase-3 expression) and (6) reversed the redox state imbalance. The results clearly show that TIIA has a prominent protective effect against SCI through inhibiting the inflammatory response and apoptosis in the spinal cord tissue after SCI.
Sprache
Englisch
Identifikatoren
ISSN: 1932-6203
eISSN: 1932-6203
DOI: 10.1371/journal.pone.0038381
Titel-ID: cdi_plos_journals_1325003310
Format
Schlagworte
Abietanes - pharmacology, Abietanes - therapeutic use, Aging - drug effects, Aging - pathology, Animals, Apoptosis, Apoptosis - drug effects, Astrocytes, Astrocytes - drug effects, Astrocytes - pathology, Bcl-2 protein, Biology, Biomarkers - metabolism, Caspase, Caspase-3, Cytokines, Cytokines - metabolism, Damage assessment, Edema, Infiltration, Inflammation, Inflammation - complications, Inflammation - drug therapy, Inflammation - pathology, Inflammation - physiopathology, Inflammation Mediators - metabolism, Inflammatory response, Injury prevention, Interleukin 6, Kinases, Male, MAP kinase, MAP Kinase Signaling System - drug effects, Medicine, Neutrophil Infiltration - drug effects, NF-kappa B - metabolism, NF-κB protein, Nitric oxide, Nitric Oxide Synthase Type II - metabolism, Nitric-oxide synthase, Oxidative stress, Oxidative Stress - drug effects, Peroxidase, Pharmacology, Rats, Rats, Sprague-Dawley, Recovery of Function - drug effects, Redox properties, Rodents, Salvia miltiorrhiza, Signaling, Spinal Cord - drug effects, Spinal Cord - enzymology, Spinal Cord - pathology, Spinal Cord - physiopathology, Spinal cord injuries, Spinal Cord Injuries - complications, Spinal Cord Injuries - drug therapy, Spinal Cord Injuries - pathology, Spinal Cord Injuries - physiopathology, Trauma, Tumor necrosis factor-TNF, Tumor necrosis factor-α, Wounds and Injuries - complications, Wounds and Injuries - drug therapy, Wounds and Injuries - pathology, Wounds and Injuries - physiopathology

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