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Background and Objective: Neurons are injured under physical, chemical and pathological conditions. The effects of injuries in peripheral nervous system returns as retrograde to the cell body of neurons in central nervous system and causes brain and spinal degeneration. This study was done to evaluate the effect of aquatic extract of Cannabis sativa leaves on degeneration of alpha motoneurons in spinal cord after sciatic nerve compression in Rats.

Materials and Methods: This experimental study was carried out on thirty two male Wistar rats, weighing 300-350 grams. Animals were divided into four groups each consisting eight members A: control, B: compression, C: compression + treatment with 25 mg/kg aquatic extract, D: compression + treatment with 50 mg/kg aquatic extract. In order to induce compression in B, C and D, after cutting the right thigh muscle, Sciatic nerve of thigh was exposed to compression for 60 seconds using locker pincers. The first extract injection was done intraperitoneally immediately after compression and the second intera peritoneal injection was done 7 days later. 28 days after compression, the Lumbar spinal cord were dissected, fixed and stained with toluidine blue. The density of alpha motoneurons was measured using dissector and stereological methods. Data was analyzed with using Minitab-13 software, ANOVA and Tukey tests.

Results: Neuronal density was 611.5±34.2 and 1633.4±30.7 in compression and control groups respectively (P<0.001). There was a meaningful statistical increase in neuronal density of group C (1278.6±28.1) in comparing compression group (P<0.001). The neuronal density in group (D) (1549.8±87.7), significantly increased in comparison with group (B) (P<0.001).

Conclusion: This study showed that aquatic extract of Cannabis sativa leaves increases the density of alpha motoneurons in spinal cord after sciatic nerve compression in Rats. The increase in neuronal density is relevant to the amount of extract used.

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Background and Objective: After axotomy or the compersion the nerve, the death of spinal cord nerves cell body occur. Compersion is one of the factors causing the degeneration of the spinal cord cell body. This degeneration is due to the reversed factors of the damaged area that have reached to cell body. Prosopis farcta is a member of leguminosae family and mimosaceae subfamily. The purpose of this study was to investigate the effect of ethanolic extract of pod prosopis farcta plant, on neuronal density of anterior horn following sciatic nerve compression in rat. Materials and Methods: This experimental study was performed on thirty male wistar rats with the age of about three months years and 300-350 gr weight. The animals were divided into five groups. A) control, B) compression, C) compression + treatment with 25 mg/kg ethanolic extract, D) compression + treatment with 50 mg/kg ethanolic extract and E: compression + treatment with 75 mg/kg ethanolic extract. After anesthetizing the rats, the muscle of thigh was splited and the sciatic nerve was kept under compersion, the muscle and skin were stitched subsequently. In the experimental groups the alchoholic extract of the prosopis farcta was injected to the rats with 25mg/kg, 50mg/kg, 75mg/kg dosage by the intrapritoneal way weekly. After 28 days of compresion, the rat, were put under the perfusion method and some samples were taken of their lumbar spinal cord and after tissue processes, 7 micron slide were provided of the samples serially. Slides were stained by toluidin blue, and some photos were taken and neuronal density of the alpha motoneurons alpha anterior horn of the spinal cord was calculated by the disector method. Data were analyzed using Minitab software, ANOVA and t- tests. Results: The neuronal density in the compression group (628±29.7) was decreased significantly in compare to the control group (1562±35.3) (P<0.05). The neuronal density in group C (1070±91), increased significantly in compare to the compression group (p<0.05). The neuronal density in group D (1117±62.8) and group E (1669±86.5) significantly increased in compare to the compression group (P<0.05). Conclusion: This study showed that alchoholic extract of the prosopis farcta has a neuroprotective effect following sciatic nerve compression in rats.

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Background and Objective: Degeneration of neurons in the central nervous system occurs during aging. Transplantation of neural stem cells (NSCs) can be preventing the degeneration of neurons. In addition to neuronal replacement, with the production of neurotrophic factors, increased survival and proliferation of endogenous cells. This study was done to compare the cell proliferation, neurotrophic factors expression and features of NSCs harvested from different areas of the central nervous system in vitro. Materials and Methods: In this laboratory study NSCs have been harvested from subgranular zone (SGZ), subventricular zone (SVZ) and central canal of spinal cord from adult Wistar rats with mechanical, enzymatical digestion and subsequently was cultured in α-MEM medium supplemented with serum as monolayer or adherent conditions and passaged for 13 times. Immunocytochemistry was used to determine expression of the nestin and GFAP markers. Semi-quantitative RT–PCR was used to confirm genes expression (NGF, CNTF, NT3, NT4/5, GDNF and BDNF). Results: Morphological features of stem cells extracted from different regions of the central nervous system were similar in the culture. Doubling time NSCs in the SVZ (37.45 hr) is shorter than in the SGZ (44.04 hr) and central canal of spinal cord (57.22 hr). The culture conditions as well as monolayer neural stem cells are capable of producing neurospheres. Also, nestin and GFAP markers, expressed by NSCs. Neurotrophic gene expression pattern profiles were similar to each other in stem cells extracted from the SGZ, SVZ and central canal of spinal cord. Conclusion: Neurotrophic gene expression in stem cells extracted from different regions of the central nervous system were similar, but proliferation capacity was higher in NSCs, which have been harvested from the SVZ.

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Background and Objective: Previous studies have shown the adverse effects of gestational diabetes on hippocampal neuron density in animal model. This study was conducted to determine the effect of gestational diabetes on number of motor neuron in the ventral horns of spinal cord in 4, 8 and 12 weeks rat offspring. Materials and Methods: In this experimental study, 30 Wistar dams were randomly allocated in control and diabetic groups. Dams in diabetic group were received 40 mg/kg/bw of streptozotocin (STZ) at the first day of gestational day (GD) and control group were received an equivalent volume normal saline, intraperitoneally. Six offspring of cases and controls were randomly selected at the 4, 8, 12 postnatal weeks. Postnatal rats were scarified and sections (6 micrometer) were taken from the cervical part of spinal cord, stained by cresyl violet. A photograph of sections was produced using an Olympus BX51 microscope and a DP12 digital camera. The number of motor neurons in the right ventral horns of spinal cord was evaluated in 100000 μm2 area of spinal cord using OLYSIA Autobioreport software. Results: The number of motor neurons in 4 weeks rat offspring were reduced (24.90%) in gestational diabetics compared to controls (17.16±0.5 vs22.85±2.1, P<0.05). The motor neurons in 8 weeks rat offspring were reduced (32.95%) in gestational diabetics in comparison with controls (17.70±1.7 vs26.40±2.0, P<0.05). Also, the number of motor neurons in 12 weeks rat offspring were reduced (24.38%) in gestational diabetics in comparison with controls (17.83±0.7 vs23.58±1.4, P<0.05). Conclusion: The uncontrolled gestational diabetes reduces the number of motor neurons in the ventral horn of spinal cord in rat offspring.

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Background and Objective: Different organizers are involved in spinal cord development and differentiation by sending various messages. Specific glycoconjugates secreted from the cells of lateral wall of spinal cord can also act as neurogenesis and neural differentiation messengers. This study was carried out to determine the distribution of sugar compounds in the lateral walls of spinal cord during mice morphogenesis using lectin histochemistry method. Methods: In this experimental study, sections of BALB/c mice from 10-16 embryonic days were fixed in formalin and then histological sections were prepared. Tissue samples for reaction to the glycoconjugates were incubated with DBA, OFA, GSA1B4 and MPA lectins. Alcian blue with pH equal 2.5 was used for background staining. Results: DBA lectin did not react with the lateral wall of the spinal cord. MPA lectin showed severe reaction but consistent, especially in nerve fibers of the lateral wall of spinal cord. GSA1B4 lectin showed weak reaction in the cells and nerve fibers of the spinal cord, but severe reaction was clearly observed in blood vessels. OFA lectin showed severe reaction with α-L-Fucose terminal sugar in the lateral walls of the spinal cord in early stages of morphogenesis. Conclusion: The most reaction in the lateral walls of the spinal cord was related to OFA, which reflects the importance of fucose terminal sugar by connecting (1→6) to the penultimate sugar N-acetyl-D-glocosamin (Glc-Nac) in the development of spinal cord. Due to severe reaction of GSA1B4 to blood vessels of spinal cord, use of this lectin for vascular studies, is recommended.

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Background and Objective: Because of tissue variety, signs, symptoms, and higher mortality and morbidity, central nervous system (CNS) tumors are of special importance in diagnosis and treatment. Knowledge of the epidemiology of these tumors helps with health system planning. This study aimed to obtain more data on the epidemiologic specifications of these neoplasms.
Methods: This descriptive-analytical study focuses on 141 patients (58 Male and 83 female) with CNS tumors who visited the 5th Azar Hospital, Gorgan, Iran, during 2013-17. All the data were obtained from hospital medical records in the Neurosurgery and Oncology Department. All demographic data were recorded, such as age, sex, tumor type, signs, symptoms, and risk factors. In cases with incomplete data, the files were completed with interviews and phone calls.
Results: The tumors in 94 (66.6%) patients were benign, and 47 (33.3%) patients had malignant and metastatic tumors. The most common signs were headache (n=43, 30.5%) and convulsion (n=24, 17%). No relationship was found between CNS tumors, diabetes mellitus, hypertension, and hyperlipidemia.
Conclusion: Regarding the high mortality of CNS tumors, early adequate attention to signs and symptoms helps earlier diagnosis. However, more studies on larger samples are needed to find more risk factors.