Neurotherapeutic and antioxidant response of D-ribose-L-Cysteine nutritional dietary supplements on Alzheimer-type hippocampal neurodegeneration induced by cuprizone in adult male wistar rat model.
Study Goal
The researchers aimed to determine whether D-Ribose-L-Cysteine (DRLC) could mitigate cuprizone-induced cognitive impairment, oxidative stress, and hippocampal neurodegeneration in rats.
Results Summary
DRLC administration attenuated cuprizone-induced memory decline, hippocampal damage, and oxidative stress while restoring antioxidant markers, enzyme activities, and neurotransmitter levels. The study did not report adverse effects from DRLC but was limited to animal models.
Population
Adult male Wistar rats (150-200g).
Effective Dosage
100 mg/kg body weight, administered once daily via oral gavage.
Duration
45 days.
Interactions
None mentioned.
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
0.5% cuprizone diet | increase | cognitive impairment and neurodegeneration | adult wistar rats | - | causes | #1 |
0.5% cuprizone diet | increase | oxidative stress | adult wistar rats | - | causes | #2 |
0.5% cuprizone diet | decrease | significant memory decline | adult wistar rats | - | caused | #3 |
0.5% cuprizone diet | increase | hippocampal alterations | adult wistar rats | - | caused | #4 |
0.5% cuprizone diet | decrease | levels of antioxidant markers | adult wistar rats | - | caused | #5 |
0.5% cuprizone diet | decrease | enzyme activities | adult wistar rats | - | caused | #6 |
0.5% cuprizone diet | decrease | neurotransmitters activities | adult wistar rats | - | caused | #7 |
0.5% cuprizone diet | increase | norepinephrine | adult wistar rats | - | caused | #8 |
0.5% cuprizone diet | increase | oxidative stress markers | adult wistar rats | - | caused | #9 |
100 mg/kg bw of DRLC | increase | memory decline | adult wistar rats | - | attenuated | #10 |
100 mg/kg bw of DRLC | decrease | hippocampal alterations | adult wistar rats | - | attenuated | #11 |
100 mg/kg bw of DRLC | increase | decrease levels of antioxidant markers | adult wistar rats | - | attenuated | #12 |
100 mg/kg bw of DRLC | increase | enzyme activities | adult wistar rats | - | attenuated | #13 |
100 mg/kg bw of DRLC | increase | neurotransmitters activities | adult wistar rats | - | attenuated | #14 |
100 mg/kg bw of DRLC | decrease | increase in norepinephrine | adult wistar rats | - | attenuated | #15 |
100 mg/kg bw of DRLC | decrease | oxidative stress markers | adult wistar rats | - | attenuated | #16 |
100 mg/kg bw of DRLC | decrease | neuropathological alteration induced by cuprizone | adult wistar rats | - | ameliorated | #17 |
INTRODUCTION: Cuprizone is a neurotoxicant causing neurodegeneration through enzymes inhibition and oxidative stress. D-Ribose-L-Cysteine (DRLC) is a powerful antioxidant with neuroprotective properties. This study explored the antioxidant response of DRLC against cuprizone-induced behavioral alterations, biochemical imbalance and hippocampal neuronal damage in adult wistar rats. MATERIALS AND METHODS: Thirty two (32) adult male wistar rats (150-200g) were divided into four groups (n = 8). Group A received normal saline only as placebo; Group B received 0.5% cuprizone diet only; Group C received a combination of 0.5% cuprizone diet and 100 mg/kg bw of DRLC and Group D received 100 mg/kg bw of DRLC only. The administration was done through oral gavage once daily for 45 days. After the last treatment, neurobehavioral tests (Morris Water Maze and Y maze) was conducted; animals sacrificed and brain harvested for histological analysis and biochemical estimations of levels of antioxidants, oxidative stress markers, neurotransmitters and enzyme activitties. RESULTS: The results showed significant memory decline, hippocampal alterations, decrease levels of antioxidant markers, enzyme and neurotransmitters activities with concomitant increase in norepinephrine and oxidative stress markers in cuprizone induced rats relative to normal but was attenuated with DRLC administration. CONCLUSION: Cuprizone causes cognitive impairment and neurodegeneration through oxidative stress; however, administration of DRLC ameliorated neuropathological alteration induced by cuprizone.