4.1 Article

Effectiveness of low-power laser therapy in improvement of the peripheral neuropathy induced by xenobiotics in rats

Journal

BIOCHEMISTRY AND BIOPHYSICS REPORTS
Volume 27, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.bbrep.2021.101085

Keywords

Low-power laser therapy; Dichloroacetate; Neuropathy; Gabapentin

Funding

  1. National Research Centre, Giza, Egypt [010010318]

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The study aimed to evaluate the efficacy of low-power laser therapy (LPLT) in managing peripheral neuropathy induced by xenobiotics in a rats' model. The results showed that LPLT was more effective than gabapentin in improving pain sensations and memory deterioration. Biochemical analysis revealed that LPLT significantly decreased beta-endorphin levels and normalized inflammatory cytokines levels, while gabapentin did not have the same effects.
Background: Peripheral neuropathy (PN) is the damage and dysfunction of neurons of the peripheral nervous system. The present study was conducted to estimate the effectiveness of low-power laser therapy (LPLT) in the management of PN in a rats' model. Methods: PN was induced by giving dichloroacetate (DCA) (250 mg/kg/day) for up to 12 weeks. Four groups of rats were used: control group, PN group, PN group treated with gabapentin and PN group treated with LPLT. The study was conducted for 8 weeks. The management of PN was estimated by behavioral tests which included hot plate and Morris water maze tests. Blood biochemical analysis were carried out. Results: Using of hot plate test indicated thermal hypoalgesia and using Morris water maze test showed cognitive decline in PN rats. Treatment with LPLT or gabapentin improved both the pain sensations and deteriorated memory that occurred in the PN rats. Biochemical analysis showed that LPLT significantly decreased the elevated beta-endorphin level in PN rats, while gabapentin could not reduce it. Treatment PN rats with LPLT or gabapentin shifted the high levels of TNF-alpha, IL-113 and IL-10 cytokines back to their normal values. Serum nitric oxide and MDA significantly increased in the PN group together with significant reduction in the rGSH level, these values were significantly improved by LPLT application while this was not the case with gabapentin treatment. Furthermore, treatment with gabapentin or LPLT significantly reduced serum ALAT and ASAT activities which are otherwise increased in the PN group. S100B, PGE2, total cholesterol, triglycerides, LDL-cholesterol, HDLcholesterol, urea and creatinine showed insignificant changes among all groups. Conclusions: Our results showed that treatment with LPLT is more efficient than gabapentin in ameliorating the peripheral neuropathy induced by xenobiotics.

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