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Effects of The Anti-glucagon Treatment (Amylin) on Isolated Hearts Performance in Experimentally Induced Type II Diabetes in Rats 胰高血糖素治疗(胰淀素)对实验性II型糖尿病大鼠离体心脏功能的影响
Pub Date : 2022-07-01 DOI: 10.21608/besps.2022.121958.1120
Yasmin Assal, N. Saleh, B. elKafoury, Ghida Hassan, H. Saleh, Mohamed Hassan Elsayed
Background/Aims: Patients with type II diabetes (T2D) have underlying pathophysiological mechanisms that increase their cardiovascular disease risk. Anti-glucagon medications as amylin and its analogs are emerging antihyperglycemic agents which recently have gained attention. However, studies exploring cardiovascular effects of amylin have shown mixed outcomes. We, therefore, aimed to assess the effects of amylin on cardiac performance in experimentally induced T2D in rats. Methods: This study was carried out in a total duration of 5 weeks on 40 adult female Wistar Albino rats were allocated into 3 groups (control group, diabetic group and a group of diabetic rats treated with amylin). Rats in the diabetic and amylin treated groups were rendered diabetic by receiving high fat diet for 2 weeks, then subjected to a single intraperitoneal (i.p.) injection of streptozotocin (STZ) in a dose of 35 mg/Kg dissolved in 1 mL of 0.05 M citrate buffer. Rats in the amylin group were treated with amylin which was started at the fifth week in a dose of 20 μg/Kg once daily for 7 days. ECG as well as the in vitro responses of isolated hearts to isoproterenol infusion by Langendorff’s preparation were also assessed. Blood samples were collected for biochemical measurements of fasting blood glucose, plasma insulin, glucagon, HbA1c and serum lipid profile. Results: Median baseline peak developed tension (PT) and PT per left ventricular weight (PT/LV) were significantly lowered in the diabetic group compared to the control group. Both parameters in the amylin treated group were significantly increased compared to the diabetic group and approached the normal control values. As regards cardiac responses to isoproterenol infusion, maximal and delta changes of heart rate (HR), PT and PT/LV were significantly decreased in the diabetic group compared to the control group. Whereas these parameters were significantly elevated in the amylin treated group compared to the diabetic group. Maximal and recovery HR values as well as maximal PT and PT/LV became normalized in the amylin treated group. The diabetic group also showed significant prolongation of time to peak tension (TPT), half relaxation time (HRT) and decrease of tension generation per unit time (TGPT), myocardial flow rate per left ventricular weight (MFR/LV) maximal responses to isoproterenol compared to control group. Those parameters were significantly improved in the amylin treated group and reached the control values, but the maximal responses of MFR/LV remained significantly lowered compared to the control group. Biochemically, amylin treatment lowered plasma glucagon level compared to diabetic and to control groups but did not increase plasma insulin level compared to diabetic group and remained significantly lowered compared to control group. Conclusions: Amylin, the anti-glucagon therapy, was able to impose partial improvement on cardiac chronotropic, inotropic functions and myocardial blood flow in diabetic
背景/目的:II型糖尿病(T2D)患者具有潜在的病理生理机制,可增加其心血管疾病的风险。抗胰高血糖素药物,如胰高血糖素及其类似物,是近年来备受关注的新兴的抗高血糖药物。然而,探索胰淀素对心血管的影响的研究显示出不同的结果。因此,我们旨在评估胰淀素对实验性T2D大鼠心脏功能的影响。方法:将40只成年雌性Wistar Albino大鼠分为3组(对照组、糖尿病组和糖尿病大鼠胰淀素治疗组),实验时间为5周。糖尿病组和胰淀素组大鼠通过高脂饮食治疗2周,然后单次腹腔注射链脲佐菌素(STZ),剂量为35 mg/Kg,溶解于1 mL 0.05 M柠檬酸缓冲液中。胰淀素组大鼠于第5周开始给予胰淀素治疗,剂量为20 μg/Kg,每日1次,连用7 d。还评估了Langendorff制剂输注异丙肾上腺素对离体心脏的心电图和体外反应。采集血样进行空腹血糖、血浆胰岛素、胰高血糖素、糖化血红蛋白和血脂生化测定。结果:与对照组相比,糖尿病组的中位基线峰值发展张力(PT)和PT/左心室重量(PT/LV)显著降低。胰淀素治疗组两项指标均较糖尿病组显著升高,接近正常对照值。在异丙肾上腺素输注后的心脏反应方面,与对照组相比,糖尿病组心率(HR)、PT和PT/LV的最大变化和δ变化均显著降低。然而,与糖尿病组相比,胰淀素治疗组的这些参数明显升高。胰淀素治疗组最大HR值和恢复HR值、最大PT值和PT/LV值恢复正常。与对照组相比,糖尿病组在异丙肾上腺素作用下的峰值张力时间(TPT)、半松弛时间(HRT)和单位时间张力生成(TGPT)、每左室重量心肌流量(MFR/LV)最大反应均显著降低。胰淀素治疗组这些参数均明显改善,达到对照组,但MFR/LV的最大反应仍明显低于对照组。生化方面,与糖尿病组和对照组相比,胰淀素治疗降低了血浆胰高血糖素水平,但与糖尿病组相比,血浆胰岛素水平没有升高,与对照组相比仍显着降低。结论:胰高血糖素抗胰高血糖素治疗能够部分改善糖尿病状态心肌变时、肌力功能和心肌血流对β肾上腺素能刺激的反应。然而,这种改善没有达到控制水平,可能是由于胰高血糖素的降低,而不是由于胰岛素依赖机制。关键字
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引用次数: 0
Fetuin A Levels Among Different Grades Of Obesity With Its Potential Link To Its Complication With Elaboration Of Physical Training Effects In Rats 不同程度肥胖大鼠的胎儿激素A水平及其并发症与体育锻炼效果的潜在联系
Pub Date : 2022-07-01 DOI: 10.21608/besps.2022.111806.1115
R. El-Shaer, R. Abd-Ellatif, Eman El-Tabaa, M. Awad
We aimed to examine the link between fetuin A and different grades of obesity with its potential link to its complication and to determine the effect of exercise on its levels as well as on obesity complications. Methods: 40 male rats were classified based on adiposity index by using cluster analysis to 4 groups: G1: normal weight with no physical training n=10, G2: Overweight n=9, G3: Obese n=11 and G4: normal weight with physical training n=10. Albumin and creatinine were determined in urine and serum levels of fetuin-A, adiponectin, TNF-α, MDA, GSH, lipid profile and HOMA IR were measured. Also, liver NFkappa and renal relative AMPK mRNA expression were determined. Results: Fetuin–A, MDA, TNF-α, LDL, TG, HOMA IR, NFkappa, Adiposity index and ACR were significantly higher while adiponectin, GSH, HDL and relative AMPK mRNA expression were significantly lower in group2,3 as compared to group1,4 and as compared to each other. While, group3 showed significant increase in ACR, as compared to group1,2,4 but there was no significant change in ACR in group2. Group4 showed significant increase in adiponectin, GSH, HDL and relative AMPK mRNA expression and significant decrease in fetuin-A, TNF-α, MDA, HOMA IR, LDL ,TG, NFkappa, adiposity index and ACR as compared to group2,3. Also, positive correlation between fetuin-A and Adiposity index, ACR and NFkappa with negative correlation between it and adiponectin detected in group2,3,4.Conclusion: Fetuin-A level is directly proportional to obesity grades and its complication. Also, exercise appears to have protective role by decreasing fetuin-A level.
我们的目的是研究胎儿素A与不同程度肥胖之间的联系及其并发症的潜在联系,并确定运动对其水平和肥胖并发症的影响。方法:采用聚类分析方法,将40只雄性大鼠按肥胖指数分为4组:G1:体重正常,未进行体育锻炼n=10, G2:体重超重n=9, G3:肥胖n=11, G4:体重正常,体育锻炼n=10。测定尿白蛋白和肌酐,测定血清胎蛋白a、脂联素、TNF-α、MDA、GSH、血脂和HOMA IR水平。同时检测肝脏NFkappa和肾脏AMPK mRNA的相对表达。结果:2、3组大鼠Fetuin-A、MDA、TNF-α、LDL、TG、HOMA - IR、NFkappa、肥胖指数、ACR显著高于1、4组,脂联素、GSH、HDL、AMPK mRNA相对表达显著低于1、4组,且组间比较差异显著。与1、2、4组比较,3组ACR明显升高,2组ACR无明显变化。组4与组2、3相比,脂联素、GSH、HDL、AMPK mRNA相对表达量显著升高,胎蛋白a、TNF-α、MDA、HOMA IR、LDL、TG、NFkappa、肥胖指数、ACR显著降低。2、3、4组胎儿素a与肥胖指数、ACR、NFkappa呈正相关,与脂联素呈负相关。结论:胎儿素a水平与肥胖程度及其并发症成正比。此外,运动似乎通过降低胎儿素a水平具有保护作用。
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引用次数: 0
Protective effect of the combined use of L-carnitine and L-arginine against hepatic ischemia-reperfusion injury in rats 左旋肉碱和精氨酸联合应用对大鼠肝缺血再灌注损伤的保护作用
Pub Date : 2022-07-01 DOI: 10.21608/besps.2022.108614.1114
Magdi A. Eldamarawi, N. Nassef
Background: Hepatic ischemia-reperfusion injury (IRI) can be mainly caused by oxidative stress, decreased nitric oxide (NO) level, activation of hepatic Kupffer cells, neutrophils adhesions, increased level of intercellular adhesion molecules, and inflammatory process. Aim: Studying the ability of L-carnitine (LC) and L-arginine (LG) to protect the liver cells against the damage caused by IRI. Methods: This study was carried out on 40 male Wistar albino rats which were divided into 5 groups; shamoperated, hepatic IRI, IRI rats pretreated with L-carnitine, IRI rats pretreated with Larginine, IRI rats pretreated with both substances. Results: The pretreatment with LC and LG separately protected the liver cells against IRI damage with preservation of liver functions by significantly improving the oxidative stress and inflammatory states, increasing NO level, decreasing the expression of vascular adhesion molecules in liver tissue, and protecting the liver cells from the damage. It was obvious that LC effects were more significant on all the tested parameters except on the NO level where the LG effect was more significant. Moreover, the combined use of both LC and LG produced a highly significant improvement of all the tested parameters approaching near the control level than that observed by their separate use. Conclusion: The combined use of both LC and LG could effectively protect the liver cells from the harmful effects of IRI.
背景:肝脏缺血再灌注损伤(IRI)主要由氧化应激、一氧化氮(NO)水平降低、肝库普弗细胞活化、中性粒细胞粘附、细胞间粘附分子水平升高和炎症过程引起。目的:研究左旋肉碱(LC)和左旋精氨酸(LG)对IRI损伤肝细胞的保护作用。方法:将40只雄性Wistar白化大鼠分为5组;肝IRI,左卡尼汀预处理的IRI大鼠,精氨酸预处理的IRI大鼠,两种物质预处理的IRI大鼠。结果:LC和LG分别预处理可显著改善肝组织氧化应激和炎症状态,提高NO水平,降低肝组织血管粘附分子表达,保护肝细胞免受IRI损伤,保护肝功能。除了在NO水平上LG效应更为显著外,LC效应在所有被测参数上都更为显著。此外,LC和LG的联合使用产生了非常显著的改善,所有测试参数接近控制水平,而不是单独使用。结论:LC和LG联合使用可有效保护肝细胞免受IRI的有害影响。
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引用次数: 1
Vitamin D3 and Alpha-Lipoic Acid alleviate chronic immobilization stress induced metabolic changes in adult male rats 维生素D3和α -硫辛酸可减轻慢性固定应激引起的成年雄性大鼠代谢变化
Pub Date : 2022-03-05 DOI: 10.21608/besps.2021.102328.1112
Ienass Bahaa El-Dein, M. Ahmed, F. Mohamed, N. Soliman, Noha N Lasheen, D. Abou-Bakr
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引用次数: 0
Autophagy promotion and fibrosis inhibition by combination of GLP1 analogue and metformin decreasing the progression of type II diabetic cardiomyopathy of albino rats: Immunohistochemical study GLP1类似物联合二甲双胍促进自噬和抑制纤维化减缓2型糖尿病性心肌病进展:免疫组织化学研究
Pub Date : 2022-03-05 DOI: 10.21608/besps.2021.103465.1113
M. Hendawy, Abdelsalam Ramy, Ibrahim Mohie
Diabetic cardiomyopathy is one of the most serious chronic complications of type 2 diabetes. This study aimed to examine the therapeutic effect of GLP1 and metformin combination as oral antidiabetic drugs on diabetic cardiomyopathy through promotion of oxidative stress, improvement of autophagy of the cardiomyocytes and regression of cardiac fibrosis. Type 2 diabetes mellitus was induced by feeding the rats high fat diet for 12 week then injecting streptozotocin (30mg/kg) intraperitoneally after 4 weeks. One group of diabetic rats received metformin (30mg/kg), another group of diabetic rats received GLP1 analogue; liraglutide (75 μg/kg) and the last group of diabetic rats received combination of both drugs. After 24 hours of the experiment, the cardiac tissues were fixed in formalin and embedded in paraffin blocks to be examined histopathologically and immunohistochemically for autophogic markers (LC3 and P62). Also homogenate of heart tissues was made to measure oxidative stress markers (MDA, GSH) in the supernatant. Light microscope examination showed typical features of diabetic cardiomyopathy in diabetic group with increase in fibrous tissue interstitially and around blood vessels, which markedly improved in diabetic rats which received combination of both drugs, also combination of both drugs showed significant increase in early and late markers autophagy LC3 and P62 respectively when compared with diabetic rats, finally synergetic effect of both drug markedly improved oxidative stress (MDA,GSH activity). So we think that our study is the first study that discuss the therapeutic effect of combination of GLP1 analogue and metformin on diabetic cardiomyopathy through the antioxidative stress, antifibrotic and autophagic improving
糖尿病性心肌病是2型糖尿病最严重的慢性并发症之一。本研究旨在探讨GLP1联合二甲双胍作为口服降糖药对糖尿病性心肌病的治疗作用,通过促进氧化应激、改善心肌细胞自噬、逆转心肌纤维化。采用高脂饲料喂养大鼠12周,4周后腹腔注射链脲佐菌素(30mg/kg)诱导2型糖尿病。一组糖尿病大鼠给予二甲双胍(30mg/kg),另一组糖尿病大鼠给予GLP1类似物;利拉鲁肽(75 μg/kg)与最后一组糖尿病大鼠联合用药。实验24小时后,将心脏组织用福尔马林固定,石蜡块包埋,进行组织病理学和免疫组化检测自噬标志物(LC3和P62)。同时制备心脏组织匀浆,测定上清液中的氧化应激标志物(MDA、GSH)。光镜检查显示糖尿病组典型的糖尿病性心肌病特征,间质和血管周围纤维组织增多,两药联合用药后明显改善,两药联合用药早期和晚期标志物自噬LC3和P62较糖尿病大鼠分别显著增加。最后,两药协同作用显著改善氧化应激(MDA、GSH活性)。因此我们认为本研究是首次探讨GLP1类似物联合二甲双胍通过抗氧化应激、抗纤维化和自噬改善治疗糖尿病性心肌病的研究
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引用次数: 1
Protective Role of Platelet Rich Plasma in Cardiovascular Dysfunction and Autonomic Dysreflexia Induced by Spinal Cord Injury in Rats 富血小板血浆对大鼠脊髓损伤所致心血管功能障碍和自主神经反射障碍的保护作用
Pub Date : 2022-03-05 DOI: 10.21608/besps.2021.91404.1110
Mohamed Hassan Elsayed, S. Khedr
Background: Patients with spinal cord injury (SCI) have a high risk of cardiovascular complications during the acute phase following the trauma, affecting their prognosis and quality of life. These cardiovascular complications require prompt medical attention to avoid neurological compromisation, morbidity, and mortality. This work aims to provide an overview of the impact of platelet-rich plasma (PRP) treatment on SCI and its cardiovascular hazardous sequelae. Methods: 26 adult female Wister rats were randomly allocated into three groups; shamoperated control group, a group that underwent compression of the spinal cord at the T4 level, with no further intervention (SCI group), and a treated group with PRP following spinal cord injury at T4 level on the site of injury (SCI-PRP group). Mean arterial pressure (MAP), heart rate (HR), as well as core temperature, were recorded under basal conditions and in response to colorectal distension (CRD). Results: Under the basal condition, hypotension and hypothermia were observed during the initial 4 weeks post-injury while tachycardia was prominent all through the study starting from the 2 week onwards in the SCI rats compared to sham controls. Meanwhile, the study of cardiovascular sequelae of SCI in response to CRD revealed a marked elevation in the MAP, hyperthermia as well as bradycardia associated with ventricular/supraventricular ectopic rhythm in the SCI group which may be accounted for by autonomic dysreflexia (AD). PRP treatment ameliorated partially the cardiovascular complications under basal conditions and in response to CRD as well. Moreover, rats with SCI showed a significant increase in atherogenic index, body weight gain in addition to hypercholesterolemia and hypertriglyceridemia. This effect was blunted in the SCI-PRP group compared to the SCI group, though not normalized. Histopathological and electron microscopic (EM) examination revealed that the SCI-PRP group had more myelinated regenerating axons of the spinal cord (SC) than the injured group but fewer than the sham group. Conclusion: The application of PRP immediately to the site of SCI facilitated its regeneration, had a potential repairing effect, and prevented, at least partially, cardiovascular complications.
背景:脊髓损伤(SCI)患者在创伤后急性期发生心血管并发症的风险较高,影响其预后和生活质量。这些心血管并发症需要及时就医,以避免神经系统损害、发病率和死亡率。本研究旨在概述富血小板血浆(PRP)治疗对脊髓损伤及其心血管危险后遗症的影响。方法:将26只成年雌性Wister大鼠随机分为3组;对照组,在T4水平压迫脊髓,不进行进一步干预组(SCI组),以及损伤部位T4水平脊髓损伤后PRP治疗组(SCI-PRP组)。在基础条件下和结直肠膨胀(CRD)时记录平均动脉压(MAP)、心率(HR)和核心温度。结果:在基础条件下,损伤后最初4周,脊髓损伤大鼠出现低血压和低体温,从2周开始,与假对照组相比,在整个研究过程中,脊髓损伤大鼠的心动过速都很明显。同时,脊髓损伤心血管后遗症对CRD的反应研究显示,脊髓损伤组MAP明显升高,高热以及与心室/室上异位节律相关的心动过缓,这可能与自主神经反射障碍(AD)有关。PRP治疗可部分改善基础条件下的心血管并发症和对CRD的反应。此外,SCI大鼠除高胆固醇血症和高甘油三酯血症外,动脉粥样硬化指数显著增加,体重增加。与SCI组相比,SCI- prp组的这种效应减弱,但没有正常化。组织病理学和电镜检查显示,SCI-PRP组脊髓再生轴突(SC)多于损伤组,但少于假手术组。结论:PRP即刻应用于脊髓损伤部位,促进了脊髓损伤的再生,具有潜在的修复作用,至少部分防止了心血管并发症的发生。
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引用次数: 0
Effect of tumor necrosis factor alpha inhibition with etanercept on renal functions in L-NAME induced hypertensive rats: insights into the possible mechanisms 依那西普抑制肿瘤坏死因子α对L-NAME诱导的高血压大鼠肾功能的影响:可能机制的探讨
Pub Date : 2022-03-05 DOI: 10.21608/besps.2021.93323.1111
Mona A. Said, R. Ibrahim, M. Allam
Many studies suggest the dominant role of the inflammatory cytokine, tumor necrosis factor alpha (TNF-α) in the prognosis of hypertension and end stage renal disease (ESRD). The objective of this study was to investigate the effects of TNF-α inhibition on renal functions in Nω-nitro-L-arginine methyl ester (L-NAME) induced hypertensive rats and the potential underlying mechanisms. Four groups of rats were used in the study for 3 weeks period; normal control group, TNFα inhibitor (etanercept) group, L-NAME-induced hypertensive group and L-NAME + etanercept group. L-NAME group showed elevated systolic and diastolic blood pressure, plasma urea, creatinine, plasma renin activity, angiotensin II, kidney tissue nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, TNFα and malondialdehyde (MDA) together with decreased creatinine clearance rate and renal antioxidants. Treatment with etanercept affords antihypertensive effect and ameliorates L-NAME induced renal impairment by improving renin–angiotensin system (RAS) and NADPH oxidase as well as by attenuating oxidative stress.
许多研究表明炎症细胞因子肿瘤坏死因子α (TNF-α)在高血压和终末期肾病(ESRD)的预后中起主导作用。本研究旨在探讨TNF-α抑制对ω-硝基- l -精氨酸甲酯(L-NAME)致高血压大鼠肾功能的影响及其可能的机制。采用四组大鼠进行实验,为期3周;正常对照组、TNFα抑制剂(依那西普)组、L-NAME致高血压组和L-NAME +依那西普组。L-NAME组收缩压、舒张压、血浆尿素、肌酐、血浆肾素活性、血管紧张素II、肾组织烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶、TNFα和丙二醛(MDA)升高,肌酐清除率和肾脏抗氧化剂降低。依那西普治疗通过改善肾素-血管紧张素系统(RAS)和NADPH氧化酶以及减轻氧化应激,具有降压作用和改善L-NAME诱导的肾损害。
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引用次数: 0
Selenium Attenuates Cholestasis-Induced Liver Injury and Fibrosis by Alleviating Liver Oxidative Stress and Inflammation in Rats 硒通过减轻肝脏氧化应激和炎症减轻胆汁淤积引起的肝损伤和纤维化
Pub Date : 2022-03-05 DOI: 10.21608/besps.2021.90723.1109
N. Nassef, Fatma M. Lebda, S. E. El Agaty, Marina Atef
Background: Oxidative stress and inflammation are primarily implicated in the development and progression of liver injury during cholestasis. Selenium, a known essential antioxidant trace element, was found to provide a remarkable antioxidant and anti-inflammatory effects on various diseases. Aim: This study was planned to evaluate the possible protective effect of selenium supplementation in a rat model of chronic cholestasis. Design: Experimental study. Methods: This study was carried out on adult male rats allocated randomly into sham, 4 weeks bile duct ligated (BDL), and BDLselenium treated (BDL-Se) groups. Sodium selenite was given by gavage daily, in a dose of 100 μg/kg for 6 weeks, starting 2 weeks before the BDL. Results: BDL group presented a significant increase in serum levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), and liver levels of malondialdehyde (MDA), tumor necrosis factor alpha (TNF-α), and transforming growth factor beta 1(TGF-β1), associated with a significant decrease in serum levels of total proteins (TP) compared to sham group . Selenium supplementation significantly lowered serum levels of AST, ALT, ALP, and liver levels of MDA, TNF-α, and TGF-β1, along with a significant increase in serum TP in BDL-Se group versus BDL rats. Histological analysis of liver showed a significant attenuation of the inflammatory score and a significant decrease in the percentage area of collagen deposition in BDL-Se group versus BDL rats. Conclusion: Selenium supplementation reduces liver injury and improves liver functions in experimental cholestasis probably by its antioxidant and antiinflammatory activities, which further alleviate the liver fibrosis.
背景:氧化应激和炎症主要涉及胆汁淤积时肝损伤的发生和进展。硒是一种已知的必需抗氧化微量元素,对多种疾病具有显著的抗氧化和抗炎作用。目的:探讨硒对慢性胆汁淤积大鼠模型的保护作用。设计:实验研究。方法:以成年雄性大鼠为实验对象,随机分为假手术组、结扎4周胆管组(BDL)和胆总管硒治疗组(BDL- se)。亚硒酸钠每日灌胃,剂量为100 μg/kg,从BDL前2周开始,持续6周。结果:BDL组大鼠血清谷草转氨酶(AST)、丙氨酸转氨酶(ALT)、碱性磷酸酶(ALP)水平显著升高,肝脏丙二醛(MDA)、肿瘤坏死因子α (TNF-α)、转化生长因子β1 (TGF-β1)水平显著升高,血清总蛋白(TP)水平显著降低。与BDL大鼠相比,添加硒显著降低血清AST、ALT、ALP水平,降低肝脏MDA、TNF-α和TGF-β1水平,显著升高血清TP水平。肝脏组织学分析显示,与BDL大鼠相比,BDL- se组炎症评分明显降低,胶原沉积面积百分比明显减少。结论:硒可能通过其抗氧化和抗炎作用减轻实验性胆汁淤积肝损伤,改善肝功能,进一步减轻肝纤维化。
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引用次数: 0
Study the Role of Vitamin D on Some Brain Degenerative Disorders in Male Albino Rats 维生素D在雄性白化大鼠脑退行性疾病中的作用研究
Pub Date : 2022-01-01 DOI: 10.21608/besps.2021.76942.1102
Fatma Alzhraa Fayed, S. Elsawy, M. Shebl, Haidy Khattab
Background: Vitamin D, a steroid hormone that plays an important role in bone and calcium metabolism, now is known it has different beneficial functions and actions on various tissues and cell types. There are evidences that vitamin D implies some functions in the central nervous system as a neurosteroid hormone. Aim: Study the role of vitamin D on aluminum chloride (AlCl3) induced brain degeneration in male albino rats. Materials and Methods: This study was carried out on 50 adult male Wistar albino rats. The rats were divided into three groups: Group I (Control group) received normal saline followed by corn oil. Group II (AlCl3 treated group) received AlCl3 followed by corn oil. Group III (VD3 treated group): subdivided into Group IIIa received VD3 followed by both AlCl3 and VD3. Group IIIb: received AlCl3 followed by VD3. Behavioral tests were done. Brain tissue acetylcholinesterase activity, malondialdehyde and glutathione peroxidase were assessed. Results: The results revealed that in AlCl3 treated group, there was a significant decrease in acetylcholinesterase level and glutathione peroxidase and a significant increase in malondialdehyde compared to the control group and significant increase in acetylcholinesterase level and glutathione peroxidase, and a significant decrease in malondialdehyde in VD3 treated group compared to AlCl3 treated group; there was also improvement in behavioral parameters inVD3 treated group compared to AlCl3 treated group. Conclusion: We concluded that either the protective or the therapeutic effect of vitamin D produced significant improvement in motor impairment, learning, and memory. Keywords
背景:维生素D是一种类固醇激素,在骨和钙代谢中起着重要作用,目前已知它对各种组织和细胞类型具有不同的有益功能和作用。有证据表明,维生素D作为一种神经类固醇激素在中枢神经系统中具有某些功能。目的:研究维生素D对氯化铝(AlCl3)致雄性白化大鼠脑变性的作用。材料与方法:以50只成年雄性Wistar白化大鼠为实验对象。将大鼠分为三组:第一组(对照组)给予生理盐水加玉米油;第二组(AlCl3处理组)给予AlCl3后加玉米油。III组(VD3治疗组):又分为IIIa组,给予VD3治疗,AlCl3和VD3联合治疗。IIIb组:AlCl3 + VD3。做了行为测试。测定脑组织乙酰胆碱酯酶活性、丙二醛和谷胱甘肽过氧化物酶活性。结果:结果显示,AlCl3处理组与对照组相比,乙酰胆碱酯酶水平和谷胱甘肽过氧化物酶显著降低,丙二醛显著升高;VD3处理组与AlCl3处理组相比,乙酰胆碱酯酶水平和谷胱甘肽过氧化物酶显著升高,丙二醛显著降低;与AlCl3治疗组相比,inVD3治疗组的行为参数也有所改善。结论:我们得出结论,维生素D的保护或治疗作用对运动障碍、学习和记忆有显著改善。关键字
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引用次数: 0
COVID-19, Wide Spread and Treatment Need COVID-19,广泛传播和治疗需求
Pub Date : 2022-01-01 DOI: 10.21608/besps.2021.51022.1086
E. El-Shafey, E. Elsherbiny
Human coronavirus, hCoV-19, is highly pathogenic with severe pneumonia linked to rapid replication of the virus and worldwide spread. Originating in Wuhan China December 2019, the current COVID-19 epidemic has grown rapidly with individual-toperson infection expanding to become a pandemic-scale global health emergency. As a pandemic, COVID-19 has led many researchers from various areas of biomedicine to pursue approaches or therapies to handle the pandemic. COVID-2019 cure is in part based on the patient's own immune system. When the over-activated immune system kills the virus, a large number of inflammatory factors are produced which lead to severe cytokine storms. This appears that the key explanation for damage to these organs may be due to a cytokine storm caused by the virus. Current therapies available-including non-specific anti-viral, antibiotics to treat secondary bacterial infections and sepsis, and inflammatory corticosteroids-fail in serious disease where the hallmark is the COVID19-induced cytokine storm in the lung. Until now, however, no specific treatment has been found for this disease. Thus, there is a significant unmet need for safe and efficient care. Keywords
人类冠状病毒(hCoV-19)具有高致病性,与该病毒的快速复制和全球传播有关的严重肺炎。新冠肺炎疫情于2019年12月发源于中国武汉,疫情发展迅速,人与人之间的感染不断扩大,已成为全球大流行规模的突发卫生事件。COVID-19作为一场大流行,促使许多生物医学领域的研究人员寻求应对大流行的方法或疗法。2019冠状病毒病的治疗部分基于患者自身的免疫系统。当过度激活的免疫系统杀死病毒时,会产生大量的炎症因子,导致严重的细胞因子风暴。这似乎是对这些器官损伤的关键解释,可能是由于病毒引起的细胞因子风暴。目前可用的治疗方法,包括非特异性抗病毒药物、用于治疗继发性细菌感染和败血症的抗生素,以及炎症性皮质类固醇,在以covid - 19诱导的肺部细胞因子风暴为标志的严重疾病中都不起作用。然而,到目前为止,还没有发现针对这种疾病的特异性治疗方法。因此,对安全和有效护理的需求仍未得到满足。关键字
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引用次数: 0
期刊
Bulletin of Egyptian Society for Physiological Sciences
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