20 research outputs found

    Evaluation of analgesic effects of intrathecal eugenol in male rats

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    زمینه و هدف: اوژنول مهمترین ماده تشکیل دهنده عصاره گیاه میخک (Eugenia caryophylata) است که به طور گسترده در دندانپزشکی جهت تسکین درد و التهاب موضعی استفاده می‌شود. از آنجایی که مطالعه‌ای در زمینه تزریق داخل نخاعی اوژنول از نظر شروع و طول مدت بیدردی انجام نشده است، لذا این مطالعه با هدف ارزیابی اثرات ضددردی تجویز داخل نخاعی اوژنول از نظر شروع و طول مدت اثر آن در موش های صحرایی نر انجام شده است. روش بررسی: در این مطالعه تجربی 51 سر موش صحرایی نر نژاد ویستار در سه گروه اوژنول و سه گروه نرمال سالین قرار گرفتند. 5 روز بعد از کاتتر گذاری در نخاع از ناحیه کمر (تحت بی‌هوشی) اثرات تجویز داخل نخاعی حجم‌های مختلف اوژنول و نرمال سالین (5، 10 و 15 میکرولیتر به ازای هر حیوان) در زمان‌های قبل از کاتترگذاری، قبل از تجویز و 10، 30، 180، 360، 720 و1440 دقیقه بعد از تجویز، روی درد ناشی از قرار دادن دم در آب ºc51 بررسی و مقایسه شد. داده‌ها با استفاده از آزمون آماری ANOVA و آزمون LSD تجزیه و تحلیل شد. یافته‌ها: نتایج این تحقیق نشان داد که عمق و طول مدت بیدردی اوژنول وابسته به دوز بوده و مقادیر بالاتر باعث فلج و بی‌حرکتی طولانی مدت گردید (05/0

    Anti-diabetic effect of betulinic acid on streptozotocinnicotinamide induced diabetic male mouse model

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    Diabetes is a metabolic disease caused by abnormal insulin secretion or action. In the present study, the effects of betulinic acid (BA, a triterpene) are evaluated on glucose, α-amylase and plasma insulin levels, insulin resistance and the histopathology of pancreatic islets in streptozotocin-nicotinamide (STZNA) diabetic mice. Seventy adult male NMRI mice were randomly divided into seven groups: control, sham, diabetic, diabetic treated with BA (10, 20 and 40 mg/kg) and diabetic treated with metformin (200 mg/kg). Diabetes was induced in mice by intraperitoneal injection of streptozotocin 50 mg/kg after a dose of nicotinamide 120 mg/kg. Two weeks after treatment with BA, blood samples were collected for measuring glucose, α-amylase and insulin levels, and the pancreas was isolated for histopathology evaluation. Diabetes reduced the number and diameter of pancreatic islets, and increased α-amylase and insulin resistance. BA treatment reduced blood glucose, α-amylase and improved insulin sensitivity as well as pancreas histopathology. In addition, BA showed stronger effects on the pancreatic histology and insulin resistance compared to the metformin group

    Protective effects of gallic acid against chronic cerebral hypoperfusion-induced cognitive deficit and brain oxidative damage in rats

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    Free radical induced neural damage is implicated in cerebral hypoperfusion disorders and antioxidants have protective effects. In the present study, we examined the effect of gallic acid (GA; 100 mg/kg, p.o. for 10 days) on cognitive deficit and cerebral oxidative stress induced by permanent bilateral common carotid artery occlusion (2VO) as an animal model of vascular dementia (VD). The results showed that 2VO significantly reduced the spatial memory performance in Morris water maze as well as non enzymatic (total thiol) and enzymatic glutathione peroxidase (GPx)] antioxidant contents and increased the level of malondialclehyde (MDA) in the hippocampus and frontal cortex of vehicle-treated group as compared to sham-operated rats. Furthermore, chronic administration of GA significantly restored the spatial memory, total thiol and GPx contents and also decreased MDA levels in these tissues. GA alone did not show any change neither in the status of various antioxidants nor behavioral tests over sham values. The results demonstrate that GA has beneficial activity against 2VO-induced cognitive deficits via enhancement of cerebral antioxidant defense. Taken together, the present study suggested that GA might be useful in the treatment of VD. (C) 2014 Elsevier B.V. All rights reserved

    COX inhibition: Catalepsy and Striatum Dopaminergic-GABAergic-Glutamatergic Neurotransmission

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    Selective COX-2 and COX-1 inhibitors were administered (i.p. acutely) to normal and parkinsonian rats, followed by the analysis of the striatal dopamine, GABA and glutamate concentrations using the microdialysis technique, simultaneously, the catalepsy of animals was evaluated. Selective COX-2 inhibition showed improving effects on the catalepsy followed by decreasing the striatum glutamatergic-GABAergic and enhancing the dopaminergic neurotransmission. Nonetheless COX inhibition had no significant improving effects on damaged Substantia Nigra Pars Compacta (SNc) neurons

    Effect of Dexamethasone on Striatal Neurotransmissions in the Rats Subjected to Parkinson’s Disease Animal Model

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    Objective(s)The aim of this study was to evaluate the effects of dexamethasone on striatal dopaminergic, glutamatergic and gamma amino butyric acid (GABA) ergic neurotransmission in normal and parkinsonian rats.Materials and MethodsDexamethasone (0.15, 0.30, 0.60 and 0.8 mg/kg) was administered to normal or parkinsonian rats (i.p.) followed by the analysis of the striatal neurotransmitters concentrations. Additionally, the effect of dexamethasone on the damaged Substantia nigra pars compata (SNc) neurons has been investigated. ResultsDexamethasone resulted in decreased level of striatum glutamatergic-GABAergic and enhanced dopaminergic neurotransmission in normal and parkinsonian rats. In addition, acute treatment with dexamethasone did not improve the lesion at all. ConclusionThese findings suggest the new therapeutic mechanism of action for dexamethasone in Parkinson’s disease animal model

    Global, regional, and national burden of disorders affecting the nervous system, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021

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    BackgroundDisorders affecting the nervous system are diverse and include neurodevelopmental disorders, late-life neurodegeneration, and newly emergent conditions, such as cognitive impairment following COVID-19. Previous publications from the Global Burden of Disease, Injuries, and Risk Factor Study estimated the burden of 15 neurological conditions in 2015 and 2016, but these analyses did not include neurodevelopmental disorders, as defined by the International Classification of Diseases (ICD)-11, or a subset of cases of congenital, neonatal, and infectious conditions that cause neurological damage. Here, we estimate nervous system health loss caused by 37 unique conditions and their associated risk factors globally, regionally, and nationally from 1990 to 2021.MethodsWe estimated mortality, prevalence, years lived with disability (YLDs), years of life lost (YLLs), and disability-adjusted life-years (DALYs), with corresponding 95% uncertainty intervals (UIs), by age and sex in 204 countries and territories, from 1990 to 2021. We included morbidity and deaths due to neurological conditions, for which health loss is directly due to damage to the CNS or peripheral nervous system. We also isolated neurological health loss from conditions for which nervous system morbidity is a consequence, but not the primary feature, including a subset of congenital conditions (ie, chromosomal anomalies and congenital birth defects), neonatal conditions (ie, jaundice, preterm birth, and sepsis), infectious diseases (ie, COVID-19, cystic echinococcosis, malaria, syphilis, and Zika virus disease), and diabetic neuropathy. By conducting a sequela-level analysis of the health outcomes for these conditions, only cases where nervous system damage occurred were included, and YLDs were recalculated to isolate the non-fatal burden directly attributable to nervous system health loss. A comorbidity correction was used to calculate total prevalence of all conditions that affect the nervous system combined.FindingsGlobally, the 37 conditions affecting the nervous system were collectively ranked as the leading group cause of DALYs in 2021 (443 million, 95% UI 378–521), affecting 3·40 billion (3·20–3·62) individuals (43·1%, 40·5–45·9 of the global population); global DALY counts attributed to these conditions increased by 18·2% (8·7–26·7) between 1990 and 2021. Age-standardised rates of deaths per 100 000 people attributed to these conditions decreased from 1990 to 2021 by 33·6% (27·6–38·8), and age-standardised rates of DALYs attributed to these conditions decreased by 27·0% (21·5–32·4). Age-standardised prevalence was almost stable, with a change of 1·5% (0·7–2·4). The ten conditions with the highest age-standardised DALYs in 2021 were stroke, neonatal encephalopathy, migraine, Alzheimer's disease and other dementias, diabetic neuropathy, meningitis, epilepsy, neurological complications due to preterm birth, autism spectrum disorder, and nervous system cancer.InterpretationAs the leading cause of overall disease burden in the world, with increasing global DALY counts, effective prevention, treatment, and rehabilitation strategies for disorders affecting the nervous system are needed

    The effect of hydro-alcoholic celery (Apium graveolens) leaf extract on cardiovascular parameters and lipid profile in animal model of hypertension induced by fructose

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    Objectives:Hypertension is one of the most common diseases of the modern era. This study evaluates the effect of hydro-alcoholic celery leaf extract onsystolic blood pressure (SBP), heart rate (HR) and lipid profile in animals’ model of hypertension induced by fructose. Materials and Methods: Sprague Dawley rats were divided into five groups: 1) control group (free access to tap drinking water), 2) group receiving 200mg/kg celery leaf extract, 3) group receiving fructose 10%, and 4,5) receiving fructose and 100mg/kg or 200mg/kg of extract (n=8). In all groups, before and during the test period, SBP and HR were measured by Power lab system. Lipid profiles were determined by auto analysis. Repeated measurement and one way ANOVA were used for data analysis. PResults:The SBP in the fructose group significantly increased compared to control group (

    Locus coeruleus lesion & cold stress: Role of the central and peripheral sympathetic nervous system in rat’s late proestrous phase

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    Objective: LC/NA system is activator of hypothalamic–pituitar–adrenal (HPA) axis and cold stress triggers an equally robust increase in plasma NA. Increased LHRH content probably due to absence or decrease of NE release from the LC and positive feedback action of E2 on LH secretion show that in late proestrous phase NA, LH and E2 have a strong link. This study was conducted to evaluate the effect of central sympathetic nervous system (by LC lesion and acute cold stress induction) and peripheral sympathetic nervous system (with propranolol administration) on late proestrous phase in rat. Material and Method: One hundred eight rats were divided into control and study groups. Study group was divided into three main sub groups: LC lesion (electrolytic lesion), acute cold stress (4°C for 20 minutes) and propranolol (antagonist of sympathetic nervous system). Vaginal smears were taken for all groups and late proestrous was selective phase for this study. Statistical differences were determined by one–way ANOVA followed by the Tukey post hoc test. SPSS 11 was used for data analysis. P value ≤ 0.05 was defined as significant level. Results: LC lesion decreased only estradiol level (P≤0.001) but could increase serum level of LH like propranolol administration (7mg/kg ip) (P≤0.01). No significant changes were noted in the levels of LH and estradiol in cold stress group like the synergistic effect of LC lesion and Cold stress also synergism of LC lesion, Cold stress and propranolol. Conclusion: This study demonstrated that late proestrous phase has a critical role in LH surge and sympathetic nervous system (NA) and E2 are important and basic factors in this process
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