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Therapeutic Methods and Therapies TCIM
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1.
Turk Neurosurg ; 33(6): 976-981, 2023.
Article in English | MEDLINE | ID: mdl-37846531

ABSTRACT

AIM: To investigate the neuroprotective effect of shilajit extract in experimental head trauma. MATERIAL AND METHODS: Three groups of 33 Sprague Dawley Albino strain male rats were included in the study. Group 1 (n=11): trauma but not treated. Group 2 (n=11): trauma and treated with 0.5 mL / rat saline Group 3 (n=11): 150 mg / kg shilajit extract was administered intraperitoneally in the treatment of trauma. Following the head trauma, the indicated treatments were applied to the 2nd and 3rd groups at the first, twenty-four and forty-eighth hours. Brain tissues and blood samples were taken after the control animals were sacrificed at the 72nd hour in all groups after trauma. Sections prepared from cerebral cortex and ca1 region were examined with hematoxylin eosin and luxol fast blue staining. Total antioxidant capacity, total oxidant capacity and oxidative stress index were measured from blood samples taken after routine procedures. RESULTS: The number of red neurons and the severity of edema were significantly higher in both the cerebral cortex and the ca1 region in the group treated with trauma only and in the group administered saline after trauma compared to the group that received shilajit extract after trauma. The total antioxidant capacity increased significantly in blood samples taken only from the group treated with trauma and saline in post-trauma treatment compared to the group given post-traumatic shilajit extract, while shilajit extract given due to traumatic brain injury significantly decreased the total oxidant capacity and oxidative stress index values compared to the other groups. CONCLUSION: Shilajit extract has been shown to have a neuroprotective effect in the treatment of acute traumatic brain injury. Our study showed that shilajit may be a useful option in the treatment of secondary brain injury, in humans.


Subject(s)
Brain Injuries, Traumatic , Brain Injuries , Craniocerebral Trauma , Neuroprotective Agents , Humans , Rats , Male , Animals , Rats, Sprague-Dawley , Antioxidants , Neuroprotective Agents/pharmacology , Neuroprotective Agents/therapeutic use , Craniocerebral Trauma/drug therapy , Craniocerebral Trauma/complications , Plant Extracts/pharmacology , Plant Extracts/therapeutic use , Brain Injuries, Traumatic/drug therapy , Brain Injuries, Traumatic/complications , Oxidants
2.
Urol Int ; 71(4): 393-8, 2003.
Article in English | MEDLINE | ID: mdl-14646440

ABSTRACT

INTRODUCTION: We have investigated the volume of nerve fibers in the rat urinary bladder following systematic exposure to cold-restraint stress and capsaicin treatment. MATERIALS AND METHODS: Adult Wistar albino rats were either exposed to cold-restraint stress (vehicle group) or treated with capsaicin before exposure to cold-restraint stress (capsaicin group). In the control group, animals were neither exposed to cold-restraint stress nor given capsaicin. From each group, samples of bladder were prepared for morphological investigation and stereological evaluation of the volume of nerve fibers. RESULTS: Stress exposure was associated with urothelial degeneration, a higher incidence and degranulation of mast cell profiles in the mucosa, and an increased volume of nerve fibers in the muscular layer of the bladder wall. Capsaicin treatment prevented the stress-induced degenerative changes. In the capsaicin group, the volume of nerve fibers in the muscular layer was also significantly smaller than that in the stress group. CONCLUSIONS: Exposure of adult rats to capsaicin prevented the stress-induced degeneration of the bladder and changed the volume of capsaicin-sensitive fibers in muscular layer. We conclude that capsaicin and related compounds may be useful in treating stress-induced bladder problems.


Subject(s)
Capsaicin/administration & dosage , Nerve Fibers/pathology , Urinary Bladder/innervation , Urinary Bladder/pathology , Animals , Female , Nerve Fibers/drug effects , Rats , Rats, Wistar , Stress, Physiological , Urinary Bladder/drug effects
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