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INNOSC Theranostics and
            Pharmacological Sciences                                               Antioxidant effects of curcumin in SCI



            3.3.3. Casp-1                                      processes, are not yet fully understood. This knowledge

            The outcomes demonstrated a prominent increase in the   gap presents considerable obstacles to the development
            protein concentration of Casp-1 in the tissue samples   of effective therapeutic strategies aimed at improving
                                                                             26,27
            of Model group animals relative to those of Control   patient outcomes.   While the initial trauma and primary
            group animals (P < 0.0001). Meanwhile, no significant   injury mechanisms are often unpredictable, there is an
            differences  in the protein concentration of ASC were   urgent need for targeted interventions that can mitigate
            found between the Model+CuC20 and the Model groups   the  detrimental  effects  of secondary injury, particularly
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            (P > 0.05). Both Model+CuC40 and Model+CuC80       those related to OS and neuroinflammation.  Pre-clinical
            groups showed significant reductions in the protein   research  has  provided  compelling  evidence  for  the  role
            concentration of Casp-1 when compared to the Model   of the NLRP3 inflammasome in the pathogenesis of SCI.
            group (Figure 8, P <  0.0001 for both treatments).  The NLRP3 inflammasome is formed by the assembly of
                                                               NLRP3,  ASC,  and  Casp-1  in  response  to  both  external
            4. Discussion                                      infections and internal signaling stimuli. This assembly
            In this research, we investigated the antioxidant effects   leads to the activation of Casp-1, resulting in the release
            of  varying doses  of  CuC in  a SCI  model  utilizing  male   of pro-inflammatory cytokines such as interleukin (IL)-1β
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            Wistar rats. Our findings revealed that SCI significantly   and IL-18.  Moreover, prior studies have demonstrated
            elevates the levels of MDA, a well-established marker of   that inhibiting NLRP3 inflammasome activity can
            OS, indicating increased lipid peroxidation and cellular   effectively reduce neuroinflammation and enhance
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            damage. Concurrently, we observed a marked reduction   functional recovery in animal models of SCI.  While the
            in the body’s antioxidant defenses, evidenced by decreased   initial trauma and primary injury mechanisms are often
            levels SOD, GSH, and TAC. These results underscore the   unpredictable, our research emphasizes the urgent need
            oxidative imbalance that occurs following SCI, highlighting   for targeted interventions that can mitigate the detrimental
            the detrimental impact of OS on recovery. Furthermore,   effects of secondary injury, particularly those related to
            our study revealed that SCI led to the upregulation of the   OS and neuroinflammation. These findings suggest that
            NLRP3 inflammasome, characterized by increased protein   targeting the NLRP3 inflammasome may represent a
            levels of NLRP3, ASC, and Casp-1. This upregulation reflects   promising therapeutic approach to mitigate the adverse
            an enhanced neuroinflammatory response following SCI,   effects of neuroinflammation and improve recovery
            contributing to the overall pathological process.  following spinal cord injuries.
              SCI poses a significant global health challenge, with   In this  study, SCI was  induced in  rats by applying
            thousands of new cases diagnosed annually, frequently   an aneurysm clip to the right side of the spinal cord for
            resulting in profound and debilitating effects on   a duration of 1  min. In the treatment groups, CuC was
            individuals’ quality of life.  The intricate pathophysiological   administered through intraperitoneal injection at three
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            mechanisms that  underlie SCI,  especially  the complex   different doses: 20, 40, and 80 mg/kg. These doses were
            interactions between primary and secondary injury   selected to evaluate the dose-dependent effects of CuC on
                                                               recovery and neuroprotection following the SCI induced.
                                                               The findings of this study demonstrated that by induction
                                                               of SCI, the MDA level was increased, and the SOD and GSH
                                                               activities and TAC levels were decreased in the animals.
                                                               Consistent with our findings, Kim  et al.  demonstrated
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                                                               that following the SCI, the amount of oxidant parameters
                                                               was increased, and the levels of antioxidant parameters
                                                               were decreased.
                                                                 CuC (C H O ) is a polyphenol extracted from turmeric,
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                                                                             6
                                                               a common spice and traditional Chinese medicine. CuC
                                                               exhibits promising effects against inflammation, OS,
                                                               apoptosis, and neurodegeneration.  Our findings revealed
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                                                               that CuC-treated groups exhibited a significant reduction
            Figure  8.  CuC  effects  on  the  protein  concentration  of  Casp-1  in   in the level of MDA relative to the untreated SCI animals.
            the SCI-induced animals.   ++++ P<0.001 compared to Control group;   Model+CuC40 and Model+CuC80 animals demonstrated
            ****P<0.001 compared to Model group.
            Abbreviations:  Casp-1:  Caspase  1;  Con:  Control;  CuC:  Curcumin;   a significant increase in the levels of SOD, GSH, and TAC in
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            SCI: Spinal cord injury.                           comparison to the SCI model animals. Gao et al.  showed
             Volume 8 Issue 2 (2025)                        82                               doi: 10.36922/itps.4795
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