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Oxyberberine an oxoderivative of berberine confers neuroprotective effects in controlled-cortical impact mouse model of traumatic brain injury

神经保护 创伤性脑损伤 TLR4型 医学 药理学 小胶质细胞 麻醉 受体 内科学 炎症 精神科
作者
Priya Mounika Tentu,Mohd Rabi Bazaz,Tulasi Pasam,Arbaz Sujat Shaikh,Zia Ur Rahman,Atul Mourya,Venkata Rao Kaki,Jitender Madan,Manoj P. Dandekar
出处
期刊:International Journal of Neuroscience [Taylor & Francis]
卷期号:: 1-16 被引量:4
标识
DOI:10.1080/00207454.2023.2286209
摘要

ABSTRACTBackground Traumatic brain injury (TBI) is known as a silent epidemic that causes many deaths and disabilities worldwide. We examined the response of oxyberberine (OBB) in lipopolysaccharide-stimulated BV2 microglial cells and a controlled-cortical impact (CCI) mouse model of TBI.Methods We synthesized OBB from berberine, and also prepared OBB-nanocrystals (OBB-NC). Male C57BL/6 mice were used for CCI surgery, and post-CCI neurobehavioral deficits were assessed from 1 h after injury through 21 days post-injury (dpi).Results OBB treatment reduced the lipopolysaccharide-triggered elevated levels of reactive oxygen species, nitric oxide, and nuclear factor kappa B (NF-κB) in BV2 microglial cells, indicating a neuroprotective potential. CCI-operated mice exhibited significant neurological deficits on 1, 3, and 5 dpi in neurological severity scoring and rotarod assay. OBB (25 and 50 mg/kg/day) and OBB-NC (3 mg/kg/day) ameliorated these neurological aberrations. Mice subjected to CCI surgery also displayed anxiogenic- and depression-like behaviours, and cognitive impairments in forced-swimming test and elevated-zero maze, and novel object recognition task, respectively. Administration of OBB reduced these long-term neuropsychiatric complications, and also levels of toll-like receptor 4 (TLR4), high-motility group protein 1 (HMGB1), NF-κB, tumour necrosis factor-alpha and interleukin 6 cytokines in the ipsilateral cortex of mice.Conclusion We suggest that the administration of OBB offers neuroprotective effects via inhibition of HMGB1-mediated TLR4/NFκB pathway.KEYWORDS: Oxyberberinetraumatic brain injuryneuroinflammationBV2 cellsHMGB1TLR4NF-κBDisclaimerAs a service to authors and researchers we are providing this version of an accepted manuscript (AM). Copyediting, typesetting, and review of the resulting proofs will be undertaken on this manuscript before final publication of the Version of Record (VoR). During production and pre-press, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal relate to these versions also. The authors (PMT, MRB, TP, ASS, ZR, AM, VRK and MPD) would like to thank NIPER Hyderabad for providing all the resources and DoP, Ministry of Chemicals and Fertilizers, Government of India for providing fellowship.
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