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1.
J Chem Neuroanat ; 87: 49-53, 2018 01.
Article in English | MEDLINE | ID: mdl-28495518

ABSTRACT

The main purpose of the present study was to investigate the effects of diclofenac sodium (DS) on the total number of neurons in segment T13 of the spinal cord of offspring of pregnant rats using stereological methods. Eighteen adult female Wistar albino rats weighing 150-200g were used. Pregnant female rats were divided into three groups; a control group, a sham group and a DS (1mg/kg, intramuscular) exposed group. The DS and sham groups received injection from the 5th day of gestation to the 19th. Twenty eight days after birth, the offspring rats were perfused with 4% buffered formalin. T13, which is one of transverse spinal cord segments, were isolated and processed for routine paraffin histology. 5µm sections were obtained using a rotary microtome according to systematic random sampling strategies. Every 40th section was taken and sections were stained with modified Giemsa. All types of motor neuron cell were identified according to their morphology. In this study, the "disector-Cavalieri combination" method was used in the stereological examination of neurons. The motor neurons were counted in the right gray matter of the ventral horn in the spinal cord segment. The Kruskal-Wallis test was used for comparison the groups. In terms of motoneuron number, no significant difference among the groups was found (p>0.05). In conclusion, our results indicated that prenatal exposure to DS has no effect on the total number of motor neuron of the offspring rats.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/toxicity , Diclofenac/toxicity , Motor Neurons/drug effects , Prenatal Exposure Delayed Effects/pathology , Spinal Cord/drug effects , Animals , Female , Motor Neurons/pathology , Pregnancy , Rats , Rats, Wistar , Spinal Cord/pathology
2.
Ulus Travma Acil Cerrahi Derg ; 22(6): 526-530, 2016 Nov.
Article in English | MEDLINE | ID: mdl-28074457

ABSTRACT

BACKGROUND: The purpose of this study was to evaluate the acute effects of thymoquinone (TQ) on acute nerve injury. METHODS: A rat model of crush injury of the sciatic nerve was used. Animals were divided into 3 groups: control, trauma, and TQ treatment groups (n=6 per group). Seven days after injury, sciatic nerve specimens were obtained from the site of the injury and analyzed histologically and stereologically. Axon diameter, myelin thickness, and axon density were measured. RESULTS: There were no significant differences in axon diameter, myelin thickness, or axon density among groups. CONCLUSION: TQ has no acute therapeutic effect on acute nerve injury.


Subject(s)
Benzoquinones/therapeutic use , Disease Models, Animal , Neuroprotective Agents/therapeutic use , Peripheral Nerve Injuries/prevention & control , Sciatic Nerve/injuries , Animals , Benzoquinones/administration & dosage , Female , Nerve Regeneration , Neuroprotective Agents/administration & dosage , Random Allocation , Rats
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