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Background and Objective: Monosodium glutamate (MSG) is used as a food additive. Several studies have reported the adverse effects of Monosodium glutamate on the testis and brain. This study was performed to determine the effect of Monosodium glutamate in rat cerebellum. Methods: In this experimental study, 24 adult wistar rats randomly allocated into three groups including experiment A, experiment B and control (C). The animals in experiment A and B were received 3g and 6g of MSG thoroughly mixed with their feeds for 14 days, respectively. Animals in control group were received MSG free diet. Food and water for rats to be free in all of experimental time. The rats were sacrificed on fifteen day. The cerebellum dissected and fixed with formalin 10% buffer and stained with hematoxylin and eosin. Results: Disorders and detachment were observed in Purkinje and granular cell layers. Neural cell distribution in granular layer redeuced in the experimental groups. Cellular degenerative changes in the granular layer of the experimental B were more severe than experimental group A. The mean number of neuron of the granular layer in the experimental A, B and control groups were 2750, 2140 and 3150, respectively. Conclusion: The consumption of monosodium glutamate dose dependly causes histopathological changes and reduces the number of the cerebellumllar neurons in adult rat.

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Background and Objective: Parkinson disease (PD) is the second most common neurologic disorder that results following degeneration of dopaminergic neurons in the pars compacta of substintia nigra (SNc). The 1-methyl-1,2,3,6-tetrahydropiridine (MPTP) is a chemical neurotoxin that widely used in animal models of PD. This study was carried out to evaluate the numerical density of dark neurons (DNs) in the SNc in mice subjected to intraperitoneal and intranasal injection of different doses of MPTP. Methods: In this experimental study, 90 male adult BALB/c mice were randomly allocated into four experimental groups including: group 1 (MPTP was injected via i.p. at the dose of 20mg/kg per 2 hours for 4 times), group 2 (MPTP was injected via i.p. at the dose of 30mg/kg for 5 consecutive days), group 3 (MPTP was injected via i.n. at a single dose of 1mg/kg), group 4 (MPTP was injected via i.n. at a single dose of 1mg/kg), four sham and one normal groups. 20 days after the final injection, the animal's brain were removed and stained by toluidine blue. Numerical density of DNs was counted. Results: Intranasal injection of MPTP significantly increased density of dark neurons in the pars compacta of substintia nigra in compare to intraperitoneally injection of MPTP (P<0.05). Conclusion: Intranasal injection of MPTP is more effective manner to induce degeneration of neurons in substintia nigra in animal model of Parkinson's disease.

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Background and Objective: After chronic stress, brain volume and weight reduces and in turn, adrenal weight and volume increases. This study was performed to determine the effect of chronic stress and memantine administration within amygdala on the alterations of brain’s volume and weight ratio to volume and weight of the adrenal gland on male mice.

Methods: In this experimental study, bi- or unilateral amygdala cannulation was preformed stereotaxically. A week after recovery, animals were received different doses of memantine (1, 0.5, and 0.1 µg/mouse), five min before stress induction. Electric foot shock induced to animals for seven consecutive days. At the end of the seventh day, animals were sacrificed and their brain and adrenal glands were fixed in formalin 4%. The volume and weight was determined by mercury immersion and accurate balance respectively.

Results: Stress non- significantly reduced brain’s volume ratio to volume of the adrenal gland and brain’s weight ratio to weight of the adrenal gland. Memantine administration within amygdala inhibited stress effect. Memantine administration in low and medium doses within right and left amygdala significantly increased brain’s volume and weight ratio to volume and weight of the adrenal gland (P<0.05).

Conclusion: Memantine dose and side dependently inhibits the effect of induced stress in male mice. Also, unilateral memantine administration within the left and right amygdala was more effective.

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Background and Objective: Hippocampus is the main region in cortex of the brain that involved in epilepsy. This study was done to determine the effect of intraventricular injection of vitamin C on histological structure of dentate gyrus of hipocampus in adult male epileptic rats.

Methods: In this experimental study, 40 adult male rats were randomly allocated into 5 groups (n=8). Animals in three groups were received vitamin C at dose (12.5, 25 and 50 mg/kg/bw) during 28 days, intraventricularly after were kindled by (pentylentetrazol; 40 mg/kg). Animals in forth group were received normal saline after were kindled by (pentylentetrazol; 40 mg/kg). Animals in the fifth group were received normal saline. After 28 days, rats were anesthetized by ketamin, then structure of hypocamp dissected. Histological passage was done in samples and coronal section was carried out. The sections of samples were stained by Hematoxyline-eosin. Forty fields systematicly were counted the normal neurons in dentate gyrus. Morphological change was determined by immunohistochemical method.

Results: The mean  number of normal neurons in dentate gyrus in epileptic rats which  received 25 g/kg vitamin C was more than animals in groups which were received doses of 12.5, 25 and 50 mg/kg vitamin C (P<0.05). This mean number of normal neurons in dentate gyrus of hypocamp in epileptic rats which received normal saline was lower than control and other experimental groups (P<0.05). Extensive morphological change in neurons of dentate gyrus in epileptic rats which received normal saline were observed (P<0.05). The lowest  morphological change were observed in neurons of dentate gyrus in epileptic rats which received at dose 25 mg/kg vitamin C in compared to the other groups (P<0.05).

Conclusion: Intraventricular injection of vitamin C in epileptic rat's dose dependly had neuroprotective effect on dentate gyrus neurons.

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Background and Objective: Transaction or laceration and compression of peripheral nerves in accidents and different circumstances resulting Wallerian degeneration which go back to perikaryon through retrograde reaction. This study was done to determine the effect of alchohlic extract of Achillea wilhelmsii on density of motor neurons of spinal cord after sciatic nerve compression in male Wistar rats.

Methods: In this experimental study, 30 male wistar rats were randomly allocated into 5 groups: group A: control, group B: compression, group C: compression and treatment with 50 mg/kg/bw of ethanolic extract, group D: compression and treatment with 75 mg/kg/bw of ethanolic extract and group E: compression and treatment with 100 mg/kg/bw of ethanolic extract of Achillea wilhelmsii. After anesthetizing rats, skin and sub cutaneous muscles of right thigh were cut to sciatic nerve appears. Then, compression of sciatic nerve was done by a surgical forceps for 60 seconds, followed by suturing muscle and skin. Extract injection was done intraperitoneally for three weeks after compression. Group A and B were received normal saline. 28 days after compression, samples were prepared from lumbar spinal cord under perfusion method and histological sections were provided serially. After staining, density of motor neurons was calculated by dissector method.

Results: Neuronal density in the compression group (707±38.56) significantly reduced in compare to control group (1740±49.81), (P<0.05). Neuronal density in group C (1208±57.58), group D (1370±33.91), and group E (1437±64.46) significantly increased in compare to compression group (P<0.05), respectively.

Conclusion: Ethanolic extract of Achillea wilhelmsii increased neuronal density of rat's spinal cord after compression of sciatic nerve.

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Background and Objective: Ducrosia anethifolia (Dc.) is a medicinal odor plant contains CNS effective compounds which has been used in Iranian traditional medicine. This study was done to determine the effect of Ducrosia anethifolia (Dc.) Boiss essential oil on spatial learning and memory in adult male rats.

Methods: In this experimental study, 35 wistar adult male rats were randomly allocated into the five groups (n=7) including: control, sham (injected vehicle) and Ducrosia anethifolia (Dc.) Boiss essential oil groups 0.125, 0.25 and 0.5ml/kg/bw, intraperitonally during four days. Morris water maze test was used to assess learning and memory.

Results: Ducrosia anethifolia (Dc.) Boiss essential oil (0.5 ml/kg/bw) was significantly increased escape latency in the second and third (P<0.05) as well as forth (P<0.05) days of acquisition test in compare to control group. In addition latency to find the hidden platform was significantly decreased with 0.25 essential oil in all days except first day (P<0.05) and in essential oil- treated rats at 0.125 ml/kg/bw in the second and third days (P<0.05) in compare to the control group.  Time spent and distance travelled in target zone were significantly increased in Ducrosia anethifolia (Dc.) Boiss essential oil -treated rats (0.5ml/kg/bw) in compare to control group (P<0.05).

Conclusion: Intraperental administration of the Ducrosia anethifolia (Dc.) Boiss essential oil at doses of 0.5 and 0.25 ml/kg/bw during four days can improves spatial learning and memory in adult male rats.

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Background and Objective: The degeneration of motor neuron in anterior horn of spinal cord can be caused by compression. Hyssopus officinalis of Laminacea family demonstrate antioxidant and anti-inflammation effects. This study was done to evaluate the effect of alcoholic extract of Hyssopus officinalis leaves, on motor neuron in spinal cord after sciatic nerve compression in male rats.

Methods: In this experimental research, 60 male wistar rats were randomly allocated into six groups including; control, compression, and compression + treatment (25, 50, 75, 100 mg/kg/bw). In order to induce compression, sciatic nerve of right leg was exposed to compression for 60 second using locker pincers. Extract injected intraperitoneally in the first and second week after compression. 28 days after compression under profusion method, the lumber spinal cord was sampled. The density of motor neurons (9-20 micron) was measured using dissector and stereological method.

Results: Density of neurons in compression group (611±34) significantly reduced compared to the control group (1658±30) (P<0.05). Moreover, neuronal density was significantly increased in
25 (1179±22), 50 (1260±20), 75 (1350±15) and 100 (1120±10) mg/kg/bw doses in treatment groups in compared to the compression group (P<0.05).

Conclusion: Alcoholic extract of Hyssopus officinalis leaves exhibite neuroprotective effect on neurons in anterior horn of the spinal cord after injury. This effect probably is related to the antioxidant and anti inflammation properties in alcoholic extract of Hyssopus officinalis, dose dependly.

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Background and Objective: Neurotrophic factors increase neuron survival and growth. In addition their expression is altered in response to nerve injury. This study was done to evaluate the neuroprotective effect of n-butanol, ethylacetate, aqueous and hydro-alcoholic fractions of Anthemis nobilis extracts through nerve growth factor (NGF) gene expression after sciatic nerve injury in rats.

Methods: In this experimental study, 36 male Wistar rats were randomly allocated into 6 groups including control group, compression, compression + hydro-alcoholic extract, compression + n-butanol, compression + ethyl acetate fraction and compression + aqueous fraction with dose of 75 mg/kg/bw, respectively. Hydro-alcoholic, aqueous, n-butanol and ethyl acetate extract of Anthemis nobilis from aerial parts was prepared by soxhlet method. In control group, after anesthetizing the animals, the muscle was cut at the site of sciatic nerve without damaging and in compression and treatment group, the right sciatic nerve was compressed for 60 sec. The extract first time was injected intraperitoneally after nerve compression and the second was performed 7 days later. After 28 days, samples were prepared from the lumbar portion of spinal cord and cDNA was synthesized and total RNA was extracted. The changes in NGF gene expression evaluated using Δct and Real Time PCR methods.

Results: NGF gene expression significantly reduced in the compression group in compare to control (P<0.05). The expression of NGF significantly increased in treated groups including hydro-alcoholic extract, n-butanol, ethyl acetate and aqueous fractions in compare to compression group (P<0.05). The expression of NGF was more in hydro-alcoholic extract treated group in comparision with other factions treated groups.

Conclusion: Neuroprotective effect of of the aerial parts of Anthemis nobilis may be due to increase of NGF gene expression.

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Background and Objective: Dysfunction and loss of basal forebrain cholinergic neurons and their cortical projections are the earliest pathological events in the pathogenesis of alzheimer disease (AD). This study was done to evaluate the effect of donepezil hydrochloride on reference and working memory caused by mutual electrical lesion of the nucleus basalis magnocellularis (NBM) in animal model of AD.
Methods: In this experimental study, 56 adult male Wistar rats were allocated into 8 group (n=7) including: control (intact), NBM lesion group, which received electrically- induced lesion (0.5 m A, 3s) in NBM, Sham group (the electrode was impaled in to the NBM with no lesion), donepezil groups (lesion + 0.1, 1, 5, 10 mg/kg/bw of donepezil hydrochloride) and vehicle group (NBM lesion+ saline). Acquisition and retention testing were done by using an eight-radial arm maze, in which, the patterns of arm entries in each group was recorded for calculating correct choice, working memory errors, reference memory error and latency.
Results: The spatial learning of animals in the lesion of NBM group significantly reduced in compared to controls (P<0.05). Moreover, no effect on spatial learning was seen in the sham group compared with the lesion group. The post-lesion treatment with donepezil hydrochloride in dose-dependent manner improved the parameters of spatial memory errors in the acquisition and retention tasks in comparision with the lesion group (P<0.05).
Conclusion: Treatment with donepezil hydrochloride, dose-dependently improves cognitive impairment induced by the destruction of the nucleus basalis magnocellularis.

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Background and Objective: Memantine (MEM) an uncompetitive N-methyl-D-aspartate receptor antagonist is used for treatment of patients with Alzheimer disease. This study aimed to examine the effect of Memantine on the spatial learning and memory in electrical lesion’s model of nucleus basalis magnocellularis (NBM) in animal model of Alzheimer's disease.
Methods: In this experimental study, 56 adult male Wistar rats were allocated into eight groups: control group; lesion group, which received bilateral electrically lesion (0.5 mA, 3s) in NBM; sham group (the electrode was entered into the NBM with no lesion); Memantine groups (lesion+1 mg/kg/bw of MEM; lesion+3 mg/kg/bw of  MEM; lesion+5 mg/kg/bw of  MEM; lesion+7 mg/kg/bw of MEM) and Vehicle group (lesion+0.2 mL saline). After one week, animals were trained to perform the Y-maze task for five days. Twenty five days after training, a retention test was performed to determine long-term memory.
Results: The bilateral lesion of NBM impaired the spatial learning compared to the control and sham groups (P<0.05). No effect on spatial learning was seen in saline group compared with the lesion group. The treatment with Memantine in  lesion+MEM 3 mg/kg/bw, lesion+MEM 5mg/kg/bw and lesion+MEM 7mg/kg/bw groups significantly improved spatial learning (P<0.05). Moreover, no significant difference of memory was observed between the results in the 5th day of training and the retention test of the 30th day.
Conclusion: Treatment with memantine improves spatial learning defects in electrical leisions model of NBM of Alzheimer's disease in dose dependent manner in animal model.

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Background and Objective: Adult neurogenesis occurs in most mammalian species in two main areas of brain: 1- subventricular zone 2- the dentate gyrus of the hippocampus. Many factors such as 17-B estradiol affect neurogenesis in the hippocampus. The aim of this study was to investigate the effect of exogenous 17-B estradiol on neurogenesis and astrocyte functions in the ovariectomized mice.
Methods: In this experimental study; NMRI mice were allocated into five experimental groups including Sham, Control, Treatment with single dose of 17-B estradiol two weeks after ovariectomy (OVX) and were sacrificed 24 hours later, Treatment with single dose of 17-B estradiol two weeks after Ovx and were sacrificed 48 hours later and   Treatment with single dose of Seasame Oil 2 weeks after OVX and were sacrificed after 24 hours. Animals were transcardially perfused with paraformaldehyde. Brains were removed and its sections for cresyl fast violet staining and GFAP immunohistochemistry were prepared. Cells were counted and investigated.
Results: Neuronal density and Proliferation of hippocampal progenitor cells in the CA1 region of 17-B estradiol treated mice significantly increased up to 24 hours (P<0.05). Density of glia and particularly astrocytes in different regions of the hippocampus significantly reduced after treatment with 17-B estradiol (P<0.05).
Conclusion: Density of hippocampal CA1 neurons are influenced by 17-B estradiol. Also, density and morphology of glia cells, especially astrocytes in different regions of the hippocampus are affected by 17-B estradiol.

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Multiple sclerosis (MS) is a chronic and multiphasic autoimmune disease which affecting the nervous system. Recently, neurotrophic factor secreting cells have been proposed as one of the best sources for cell therapy in MS disease. Therefore, this review study was done with aimed to introduce neurotrophic factor secreting cells and the role of neurotrophic factors in the treatment of MS. The present study, based on the Systematic Review and using multiple sclerosis, neurotrophin and cell therapy keywords, 98 articles were searched from various databases including Pubmed, SID, Springer, SinceDirect Magiran, Web of Sciences and the Google Scholar. After removing irrelevant and repetitive articles, 50 articles were selected. The results of these studies showed that cell-based therapies in MS have been designed with the aim of replacing destroyed cells or with the goal of neuronal support using neural growth factors. Neurotrophic factors secreting cells with the ability to migrate to neurological lesions and secretion of neurotrophic factors can play a major role in supporting neural tissue and preventing its destruction. These factors, through tyrosine kinase receptors, have a variety of effects on the development and proper functioning of neurons. On conclusion, neurotrophic factor secreting cells due to the secretion of a wide range of neural growth factors which required for neural development might be one of the ideal cell sources for cell-based therapy in MS disease.

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Background and Objective: Multiple Sclerosis (MS) is a neurologic necrotic and chronic illness that causes by demyelination in CNS. One of the common clinical symptoms in MS is cognitive disorders. The most common cognitive defects in patients with MS are reduction of memory and information processing rate hippocampus functions in brain are memory and learning. This study was done to determine the function mechanism of memory discover by study on hippocampus. Nowadays tendency of herbal therapy is increased because of drug's side effects. This study's purpose that is from experimental typ effect of compaind extract of Portulaca olerace, Urtica dioica and Boswellia serrata on memory and number of neurons in CA1 area of hippocampus in induced multiple sclerosis rats.
Methods: In this experimental study 30 male adult rats were randomly allocated into control group, sham group (salin injection), (MS + salin) group, (MS + mixture extract, dose of 200 mg/kg), (MS + mixture extract, dose of 400 mg/kg). MS model was induced by intra hippocampal injection a single dose of ethidium bromide (0.01% ethidium bromide sulotion in 0.9% salin) and in 3 microlitre volume with 1 microlitre in minute rate intraperitoneally. Compaind extract of Portulaca olerace, Urtica dioica and Boswellia serrata were injected as the treatment for 21 days. The shuttle box test was used for evaluation of memory. Dissector method was used for neural density in CA1 of hippocampus. Histopathology method was used for evaluation of the alteration of cells.
Results: Neural density in MS induced group was singnificantly reduced in comparison with control and sham groups (P<0.05). Neural density was singnificantly increased in treatment groups in comparison with MS induced group (P<0.05). Histological results showed that induction of MS caused the disrution of neuron cells in compare to controls, but intraperitonal injection of compaind extract cause neurogenesis in tertment groups. Memory in MS induced group was singnificantly reduced in comparison with control and sham groups (P<0.05), but memory was singnificantly increased in treatment groups in comparison with MS induced group (P<0.05).
Conclusion: Compaind extract of Portulaca olerace, Urtica dioica and Boswellia serrata with dosages of 200 and 400 mg/kg/bw due to neurogenesis and amilioration can effective in memory recovery and neural necrosis in MS disease.

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Background and Objective: Parkinson's disease is a neurological disorder caused by the loss of dopaminergic neurons in pars compacta of substantial nigra. The most important symptoms of this disease include slow motion, lack of movement, tremor and imbalance. This study was done to determine the effect of probiotic Lactobacillus paracasei on motor disorders caused by injection of 6-hydroxy dopamine in Parkinson's model in male rats.
Methods: In this experimental study, 48 male rats were randomly allocated into six groups. To create an animal model of Parkinson's disease, a black body component in male rats was injected 6-hydroxy dopamine (6-OHDA) (0.5 mg/kg) unilaterally by stereotaxic apparatus. After 3 weeks of recovery, to evaluation of degradation rate, animals were received apomorphine, intraperitoneally. In the first experiment, rats were randomly divided into Sham and Parkinson's (injured) groups, the Sham group were received only water and food, and the injured group received 6-hydroxy-dopamine. In the second experiment, male rats were divided into 4 groups of 8 rats, each of the 4 groups was injected 6-hydroxy-dopamine and 21 days later, they were tested for assay of apomorphine. The results were recorded, then for 28 days, the first group was taken as control. The second group of saline, the third group of milk, the fourth group of milk and probiotic were gavaged. At the end of day 28, once again, each group was subjected to rotation of apomorphine test and the rotations were recorded.
Results: The behavioral analysis of saline, milk, milk plus probiotics were indicated that the group receiving probiotic Lactobacillus paracasei plus milk was significantly less apomorphine rotation test than the saline group (P<0.05).
Conclusion: It seems that probiotic Lactobacillus paracasei can reduces Parkinson’s disease symptoms.

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Background and Objective: Food restriction may have beneficial or detrimental effects on the brain functions such as learning and memory. Also, dopamine receptors are involved in learning and information retrieval. This study was performed to determine the simultaneous effect of food restriction and dopamine D2 receptor inhibition on spatial memory of rats.
Methods: In this experimental study, 60 male Wistar rats were allocated into 6 groups including controls, 25%, 50% and 75%, food restriction, sulpiride (D2 receptor antagonist, 4 mg/kg/day, ip), 75% food restriction and sulpiride and treated for 21 days. To evaluate the memory, an eight-point radial arm maze was used. Then, the catalase and malondialdehyde level of the hippocampus were measured.
Results: Twenty-five percent food restriction caused to 11.8 percent decrease in spending time to find the food compared to control group (P<0.05). The 75% food restriction and or sulpiride injection significantly increased that time by 24.4% and 18.3%, respectively (P<0.05). The group with 75% food restriction were received sulpiride showed the most increase in the time of food finding compared to all groups (P<0.05). Catalase activity was only significantly reduced in the 75% restricted groups to 17.6% and 22.2%, respectively (P<0.05). Malondialdehyde production was significantly increased in the 75% food restricted groups to 50.2% and 59.3, respectively and sulpiride-received group to 31.2% compared to the control group (P<0.05).
Conclusion: Simultaneous applying of food restriction and inhibition of dopamine D2 receptors resulted in increased hippocampal prooxidant levels and exacerbated memory impairment.

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Background and Objective: Early diagnosis of Alzheimer's disease (AD) seems necessary due to the high cost of care and treatment, the uncertainty of existing therapies, as well as the worrying future of the patient. This study was conducted to AD diagnosis by MRI images using artificial intelligence methods.
Methods: In this research, a computer system for early detection of AD with using machine learning algorithms is presented in the framework of computer-aided process. Conditional random field and Inception deep neural network have been adapted for brain MR images to detect AD. Since hippocampal tissue is one of the first tissues to be affected by AD, hence for the early detection of this disease, the hippocampus was located from other brain tissues firstly and then due to the extent to which this tissue is affected, the diagnosis was made. Conditional random field could accurately extract hippocampal fragments of different shapes in all three brain planes. These components serve as the basis for feature extraction by the deep network. The proposed method was tested on standard ADNI dataset images and its performance was demonstrated. The used Inception network has been trained on the huge ImageNet dataset. One of the important steps is knowledge transfer of the problem under consideration. To facilitate this, data augmentation process was applied according to the shape and structure of the hippocampus.
Results: The implemented method in this research, achieved to 98.51% accuracy for two-class classification of "Alzheimer" versus "Normal control" and achieved to 93.41% accuracy for two-class classification of "Mild cognitive impairment" versus "Normal control", which increased by 2.56% and 8.41%, compared with the rival methods, respectively.
Conclusion: The achieved results of this study showed that the using of artificial intelligence techniques has highly accurate in diagnosing AD according to MRI images.

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Background and Objective: Multiple sclerosis (MS) is a common neurological disease that increases oxidative stress and causes immune system disorders. Curcumin is the active component of turmeric with anti-inflammatory properties. This study was conducted to determine the effects of curcumin on cortisol, catalase, and nerve growth factor (NGF) expression in an animal model of MS.
Methods: This experimental study was conducted on 30 female Wistar rats. Experimental autoimmune encephalomyelitis (EAE) was chosen as an experimental model of MS. The rats were divided into 3 groups of 10, including a healthy control group, an affected group, and a group treated with curcumin. The disease was induced by immunization of rats with homogenized guinea pig spinal cord and Freund's complete adjuvant. Then, the immunized animals were allocated into two equal groups. Treatment with curcumin (100 mg/kg daily) was started 12 days after the immunization when the rats showed the first symptoms of neurologic disability. The treatment was continued until day 24 post-immunization. Simultaneously, the EAE group received the medicine solvent (distilled water). Finally, the rats' weights as well as cortisol, catalase, and NGF levels were measured in the study groups.
Results: Curcumin significantly increased the level of cortisol to a level equal to that of healthy rats (P<0.05). It also significantly increased the expression of NGF and reduced the amount of catalase in the affected rats (P<0.05). The curcumin administration significantly increased the overall weight of rats with MS but had no significant effect on the spleen weight of the treated rats.
Conclusion: Curcumin can be beneficial for treating EAE by reducing the destructive effects of oxidative damage and increasing NGF.
 

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Background and Objective: Acrylamide is a neurotoxic agent that increases oxidative stress by creating an imbalance between the production and removal of free radicals, which in turn contributes to the pathogenesis of some neurodegenerative disorders. Thymoquinone extracted from Nigella satvia has prominent antioxidant effects. The objective of this study was to evaluate the effects of thymoquinone on hippocampal oxidative stress and neuronal density following acrylamide administration in male rats.
Methods: In this experimental study, 28 male Wistar rats aged 10-12 weeks and weighing 180-200 g were randomly divided into 4 groups of 7 rats: control, acrylamide, acrylamide + thymoquinone treatment (1 mg/kg), and acrylamide + thymoquinone treatment (5 mg/kg). For induction of brain injury, 50 mg/kg of acrylamide was injected intraperitoneally. Two days after the acrylamide injection, the rats were sacrificed, and malondialdehyde (MDA), glutathione (GSH), and catalase levels were measured in hippocampal homogenate. Evaluation of neuronal density in hippocampal CA1 region was also performed by Nissl staining.
Results: Acrylamide injection significantly increased MDA level and reduced GSH content and catalase activity in comparison with the control group (P<0.05). Administration of 5 mg/kg thymoquinone significantly reduced MDA level (P<0.05) but improved GSH and catalase activity in comparison with the acrylamide group (P<0.05). In addition, neuron density of hippocampal CA1 region did not differ significantly between the groups.
Conclusion: Thymoquinone can attenuate oxidative stress markers in a dose-dependent manner.
 

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Background and Objective: Temporal lobe epilepsy is characterized by the degeneration of hippocampal neurons and the sprouting of mossy fibers in the dentate area. This study aimed to investigate the impact of the hydroalcoholic extract of Rosa damascene on hippocampal tissue changes induced by kainic acid-induced epilepsy in rats.
Methods: In this experimental study, 28 male Wistar rats weighing between 185-225 grams were used. The animals were divided into four groups: sham group, sham treated with hydroalcoholic extract, epilepsy (kainic acid), and epilepsy pretreated with hydroalcoholic extract. Kainic acid was used for intra-hippocampal and unilateral injection to induce epilepsy in the animals at 0.8 micrograms per rat. The rats were given 500 mg/kg of the extract intraperitoneally daily for one week before surgery. Five weeks after surgery, thionin and Tim staining methods were performed on the hippocampal slices.
Results: Kainic acid-induced epilepsy resulted in convulsive behavior, and pretreatment with the hydroalcoholic extract significantly reduced the intensity of convulsive attacks (P<0.05). The density of neurons in the CA3 area of the hippocampus in the kainic acid group showed a significant decrease compared to the sham group (P<0.05), while pretreatment with the extract caused a significant increase in the number of neurons in this area compared to the kainic acid group. Additionally, a significant increase in the intensity of mossy fiber sprouting was observed in epileptic rats compared to the sham group, and pretreatment with the extract significantly decreased its intensity (P<0.05).
Conclusion: The pre-treatment with the hydroalcoholic extract of Rosa damascena decreased convulsive behavior, protected hippocampal CA3 neurons and reduced the intensity of sprouting in the hippocampal dentate region in the experimental model of temporal lobe epilepsy induced by kainic acid.
 

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Background and Objective: Demyelinating lesions, widespread tissue damage, and neuronal connectivity impairments in white matter are associated with reduced cognitive decline in multiple sclerosis (MS) patients. These findings are particularly prominent in the corpus callosum of the brain. Interleukin-10 (IL-10) is an anti-inflammatory cytokine secreted by regulatory T cells (Tregs) with anti-inflammatory properties and can inhibit the production of pro-inflammatory cytokines produced by macrophages and T cells. IL-6 is a multifunctional cytokine involved in the immune system of autoimmune diseases. The IL-6 gene consists of 5 exons, 4 introns, and a proximal promoter region located on the 7p21 chromosomal locus in humans. This study aimed to determine the effects of IL-10 (-1082/-819) and IL-6 (-174) gene polymorphisms on corpus callosum changes in women with MS.
Methods: This case-control study was conducted on 40 women with MS aged 20-40 years referring to Golestan and Kowsar Magnetic Resonance Imaging (MRI) centers in Gorgan and 20 women without MS, autoimmune or inflammatory diseases over 40 years during 2015. Ten mL of blood was taken from the subjects for genotyping. Additionally, DNA extraction was performed using the phenol-chloroform method, and DNA genotyping was performed using the sequence specific primer-polymerase chain reaction (SSP-PCR) method. Brain MRI images of the subjects were employed to measure the corpus callosum and to investigate the relationship with the investigated polymorphisms.
Results: After performing the tests and obtaining different IL-6, IL-10 (-819), and IL-10 (-1082) genotypes, no significant statistical correlation was observed between IL genotypes in the case and control groups. Additionally, no significant correlation was observed between the different IL-6, IL-10 (-819), and IL-10 (-1082) genotypes and changes in the size of different parts of the corpus callosum, including rostrum width, splenium width, body width, the ratio of body length to anteroposterior length, and the ratio of body length to maximum height between the case and control groups. Reductions in the variables of rostrum width, splenium width, body width, the ratio of body width to anteroposterior length, and the ratio of body width to maximum height were significant in both case and control groups (P<0.05). Only the reduction in splenium width was significantly associated with the occurrence of MS (P<0.009, odds ratio [OR]=2.35, 95% confidence interval [CI]=4.51-1.22).
Conclusion: There was no relationship between the morphometric changes of reduced corpus callosum and the changes in IL-6, IL-10 (-819), and IL-10 (-1082) genotypes in patients with MS.