Curcumin liposomal nanoparticles provide superior neuroprotection by attenuating neuropathic pain, neuroinflammation and anxiety in chronic sciatic nerve injury in rats.
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引用次数: 0
Abstract
Background: Chronic constriction injury (CCI) of the sciatic nerve induces neuropathic pain, inflammation, oxidative stress and neurodegenerative changes, impairing sensory and emotional function. While curcumin is well recognised for its anti-inflammatory and neuroprotective properties, its therapeutic use is limited by poor bioavailability. Curcumin liposomal nanoparticles (CLNs) offer improved delivery and stability.
Methods: Male rats (n = 24) were randomly assigned to control, CCI, CCI + curcumin (60 mg/kg) and CCI + CLNs (40 mg/kg) groups. CCI was induced through sciatic nerve ligation, followed by 14 days of treatment. Behavioural assessments included thermal and mechanical pain sensitivity, anxiety-like behaviour (elevated plus maze), and sciatic nerve function (SFI). Serum inflammatory (tumour necrosis factor-alpha (TNF-α), interleukin-6 (IL-6)) and oxidative stress markers (malondialdehyde (MDA), total antioxidant capacity (TAC), superoxide dismutase (SOD) and reduced glutathione (GSH)) were measured, alongside histological analysis.
Results: Compared to curcumin, CLNs showed superior efficacy in improving pain thresholds, anxiety-like behaviours and SFI scores. CLNs significantly lowered TNF-α and IL-6 levels and enhanced SOD activity, with no intergroup differences in MDA, TAC or GSH. Histology confirmed nerve regeneration and reduced neurodegeneration.
Conclusions: CLNs effectively alleviated neuropathic pain, reduced neuroinflammation and improved functional recovery after sciatic nerve injury, while mitigating anxiety-like behaviours.
期刊介绍:
Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs.
Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.