D-ribose-L-cysteine exhibits neuroprotective activity through inhibition of oxido-behavioral dysfunctions and modulated activities of neurotransmitters in the cerebellum of Juvenile mice exposed to ethanol.

Alcohol exposure to the cerebellum has been known to trigger cerebellar dysfunctions through several mechanisms. This present study was designed to evaluate the repealing effect of D-ribose-L-cysteine (DRLC) on alcohol-induced cerebellar dysfunctions in juvenile BALB/c mice. The animals were randomly divided into 4 groups (n = 10 per group). Mice were given oral administration of normal saline (control), DRLC (100 mg/kg, p.o), ethanol (0.2 mL of 10% w/v), or DRLC (100 mg/kg, p.o) + ethanol (0.2 mL of 10% w/v). On day 29 of the study (i.e., 24 h after the administration of the last respective doses), neurochemical quantification of the respective levels of serotonin and dopamine, lipid peroxidation, total antioxidant, superoxide dismutase, and glutathione peroxidase in the cerebellar tissues of the mice were analyzed. Compared with the saline-treated group, the studied neurochemical indices were modulated across the various experimental groups. The administration of ethanol significantly modulates the levels of monoamine neurotransmitters (serotonin and dopamine) as well as contents of total antioxidants, activities of superoxide dismutase, and glutathione peroxidase, with a concurrently increased level of lipid peroxidase in the cerebellar tissue of the mice. DRLC significantly reverses these effects in the DRLC + ethanol co-treated group. Combined exposure to DRLC + ethanol counteracts the deleterious effect of ethanol in the cerebellum of juvenile BALB/c mice via monoamine neurotransmitter, lipid peroxidation, total antioxidant status, superoxide dismutase, and glutathione peroxidase action pathways. Therefore, DRLC could be a pharmacologic or therapeutic agent in attenuating the deleterious effects of alcohol on the cerebellum.

Chromatographic and computational studies of ligands associated with bilharziasis.

OBJECTIVE: Rapid diagnostic techniques that do not depend on microscopic analysis are urgently needed for rapid diagnosis and management of bilharziasis. Specific ligands that are excreted through urine in bilharziasis may serve as rapid diagnostic biomarkers to replace microscopy, which is cumbersome and time-consuming. The aim of this study was to identify ligands associated with bilharziasis. METHODS: Microscopy was employed to detect ova of Schistosoma haematobium in urine specimens obtained from 1032 subjects. Pooled positive urine samples and pooled normal urine samples were separately prepared in triplicates and analyzed by gas chromatography-mass spectrophotometry (GC-MS). Ligands identified in each pool were noted. Computational analysis was performed between the schistosome receptors and ligands. RESULTS: GC-MS revealed that the level of indole in bilharziasis sample was higher than that in normal urine. Indole was the ligand with the highest (28.63%) concentration in the pooled positive urine sample, while ethyl phenazone level was the highest (69.64%) in the pooled normal sample. Computational analysis depicted perfect docking with indole and all other ligands identified in positive urine samples. CONCLUSION: This study identified some ligands associated with bilharziasis some unique to normal (negative) urine samples.

Heavy metals obtained from waterways induced neurodegeneration in the prefrontal cortex of Wistar rats

The level of heavy metals in Nigeria waterways is grossly influenced by the irrepressible disposal and recycling of electronic waste. The impact of heavy metals obtained from waterways on the prefrontal cortex of experimental rats was investigated in this study. Thirty (30) adult male Wistar rats weighing about 150-180 g were used in this study. Ten rats apiece were assigned randomly into three groups. Pooled sampled water and water containing the highest average concentration of combined heavy metals recorded in the waterways was given to the Wistar rats within the treatment groups ad libitum for 65 days. Blood sera were obtained for analysis of oxidative stress markers. The prefrontal cortex was processed for paraffin embedding, and sections stained for histological, histochemical and immunochemical evaluations. P < 0.05 was regarded as significant for data using one-way analysis of variance. Oxidative damage was observed in animals from the treatment groups when compared to the control. The analysed levels of oxidative stress markers showed statistically significant differences, except between groups given pooled sampled water and combined metals. Neurodegeneration was attested from the histological and histochemical evaluations, and the immunohistochemical evaluation revealed marked astrocytosis with induced oxidative stress while comparing the experimental groups

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A comparative study of the lateral geniculate body of rat (Rattus norvegicus), bat (Eidolon helvum) and pangolin (Manis tricuspis).

In this study, the lateral geniculate bodies (LGB) of rats, bats and pangolins were compared using histological and quantitative histochemical parameters to observe possible modifications that enable these mammals to cope with their habitation particularly with respect to their diet. The study was conducted using ten adult Wistar rats, ten fruit bats and eight pangolins comprising of both sexes. After being sacrificed by cervical dislocation, their skulls were opened using bone forceps to expose the brains. The lateral geniculate bodies were excised from each brain tissue, homogenized and homogenate studied spectrophotometrically for the activities of lactate dehydrogenase (LDH), glucose-6-phosphate dehydrogenase (G-6-PDH), acid phosphatase (ACP), alkaline phosphatase (ALP) and acetylcholinesterase (AChE). The LGB tissue samples meant for histological studies were fixed in 10% formol calcium and processed for paraffin wax embedding. Serial sections of 3?m thickness were stained with Hematoxylin and Eosin (H & E) and Cresyl fast violet (CFV) stains. The stained tissues were studied under the light microscope. Application of one-way ANOVA statistical method showed that there were significant differences (p<0.05) in the activities of LDH, G-6-PDH, ACP, ALP and AChE of the LGB of the three mammals as revealed in the quantitative histochemistry of these enzymes and markers. Histological observations revealed no observable differences in the relative distribution of neurons and their supporting glial cells within the LGB of the three mammalian species. The comparison of the differences observed in the histological and the quantitative histochemical activities in these mammalian species revealed a variation in the visual perception and their individual peculiarities in relation to their mode and pattern of living.