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Abstract Objective To assess the influence of oxidative stress on the gene expression of nitric oxide synthases (NOS 3 and NOS 2) and, hence, the cardiovascular responses in preeclampsia. Methods This was a case control study in which patients with preeclampsia (PE group) and normal pregnancy controls (NP group) were included according to the guidelines of the American College of Obstetricians and Gynecologists (ACOG). The serum levels of malondialdehyde (MDA), total antioxidant capacity, and nitric oxide (NO) were estimated, and the heart rate andmean arterial pressure were recorded. The gene profiling of NOS3 and NOS2 was performed through real-time polymerase chain reaction (RT-PCR). The statistical analysis was performed using the Student t-test, and values of p<0.05 were considered statistically significant. Results The serum levels of malondialdehyde were increased (p<0.0001), and the total antioxidant capacity was reduced in the PE group (p=0.034), indicating oxidative stress. In the PE group, themean arterial pressure was significantly higher (p<0.0001), but the serum levels of NO did not show a statistically significant reduction (p=0.20). The gene expression profiling of NOS3 and NOS2 revealed a down regulation in the PE group by 8.49 and 51.05 times respectively. Conclusion Oxidative stress may lead to endothelial dysfunction, which could result in increased mean arterial pressure. Nitric oxide may play a role in this mechanism, but interactions with other vasoactive /biological substances cannot be overlooked, as the gene expression of NOS3 and NOS2 has been reduced.
Resumo Objetivo Avaliar a influência do estresse oxidativo na expressão genética das óxido nítrico sintases (nitric oxide synthases, NOS, em inglês; NOS 3 e NOS 2) e, consequentemente, nas respostas cardiovasculares na pré-eclâmpsia. Métodos Este foi um estudo caso-controle no qual pacientes com pré-eclâmpsia (grupo PE) e controles comgravidez normal (grupo GN) foramincluídos de acordo com as diretrizes do American College of Obstetricians and Gynecologists (ACOG). Foram estimados os níveis séricos de malondialdeído (MDA) da capacidade antioxidante total, e de óxido nítrico (nitric oxide, NO, em inglês). A frequência cardíaca e a pressão arterial média foram registradas. O perfil genético da NOS3 e da NOS2 foi feito por reação em cadeia de polimerase em tempo real (real-time polymerase chain reaction, RT-PCR, em inglês). A análise estatística foi feita utilizando-se o teste t de Student, e valores de p<0,05 foram considerados estatisticamente significativos. Resultados Os níveis séricos de malondialdeído sérico estavam aumentados (p<0,0001), e a capacidade antioxidante total, reduzida no grupo PE (p=0,034), o que indicava estresse oxidativo. No grupo PE, a pressão arterial média era significativamente maior (p<0,0001), mas os níveis séricos de NO não demostraram redução estatisticamente significativa (p=0,20). O perfil de expressão genética da NOS3 e da NOS2 revelou uma regulação negativa no grupo PE de 8,49 e 51,05 vezes, respectivamente. Conclusão O estresse oxidativo pode levar à disfunção endotelial, o que pode resultar em aumento da pressão arterialmédia. O NO pode desempenhar umpapel neste mecanismo, mas as interações com outras substâncias vasoativas/biológicas não podem ser negligenciadas, uma vez que a expressão genética da NOS3 e da NOS2 foi reduzida.
Subject(s)
Humans , Female , Pregnancy , Pre-EclampsiaABSTRACT
Background: Blood flow, metabolic rate and oxygenrequirements of an organ guide the extent of oxidativestress experienced by any tissue in response to chronichypoxia. Currently cilnidipine is used in themanagement of hypertension and its antioxidant actionsare gaining wide interest. Aim and Objectives: Toevaluate the tissue specific effects of chronic sustainedhypoxia with regards to oxidative stress in the contextof cilnidipine. Material and Methods: Twenty fouradult male Wistar strain albino rats were randomlyassigned into four groups: group 1, control, normoxia(21% O ); group 2, chronic hypoxia (CH) (10% O ) for 2 221 days; group 3, normoxia + cilnidipine (Cil) for 21days; group 4, chronic hypoxia + cilnidipine (CH+Cil)for 21 days. Following 21 days of intervention bloodwas collected and animals were sacrificed and liver,lung and heart were collected. Serum MDA and MDAin tissue homogenate of liver, lung and heart wereestimated. Results: Our results demonstrate theelevated serum MDAlevels in chronic hypoxia exposedrats (group 2). We also observed increased MDAin liverfollowed by lung and least in the heart in chronichypoxia exposed rats (group 2). Treatment withcilnidipine reduced serum MDA and heart MDA levelsin cilnidipine treated chronic hypoxia exposed rats(group 4). However cilnidipine did not have anyinfluence on MDA levels in the liver and lung in samegroup of rats. Conclusion: The results demonstratetissue specific effects of chronic sustained hypoxia withthe highest oxidative stress observed in the liverfollowed by the lung. Although oxidative stress is alsoobserved in the heart it is the least in comparison to theliver and the lung. Cilnidipine, a dual L/N type calciumchannel blocker demonstrated beneficial antioxidantactions only in the heart supporting the cardioprotectiverole of cilnidipine
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Cadmium is one among the most environmental pollutants that affects many organs like kidney, liver and testis. The present study was aimed to assess the simultaneous effects of black tea extracts (BTE) on cadmium chloride induced alterations in lipid profile and liver histology. Adult rats were divided into four groups (n=6/group), group I (normal saline), group II (CdCl2, 1.0 mg/kg, b.wt; i.p), group III (black tea extract, 2.5 gm tea leaf/dl of water that is 2.5% of aqueous BTE) and group IV (cadmium chloride + BTE). Cadmium chloride intoxicated rats showed significant increase in serum total cholesterol, triglycerides, and low density lipoprotein-cholesterol and there is a significant decrease in the serum high density lipoproteincholesterol. In the liver, cadmium chloride showed changes in normal architecture, swollen hepatocytes, kupffer cells hyperplasia, dilation and congestion of central vein. Oral administration of black tea extracts with cadmium chloride significantly improves lipid profile and liver architecture as compared to the cadmium chloride group. The results indicate that BTE is beneficial in preventing cadmium-induced lipid alterations and hepatocellular damage.
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Among the chemical hazards, heavy metal like nickel (Ni) is considered to be a serious one. It induces severe liver and kidney damage by altering several marker enzymes and ascorbate-cholesterol metabolism. The objective of the study was to investigate the possible protective role of α-tocopherol on NiSO4 (Ni II) exposed alteration of hematological parameters, markers of liver and kidney functions, hepatic and renal antioxidant defense system in male albino rats. We have studied the effects of α-tocopherol supplementation on nickel sulfate induced alteration of body weight, hematology, liver and kidney toxicity markers (SGOT, SGPT, total protein, urea, creatinine) and hepatic and renal antioxidant defense system of male albino rats. Nickel toxicity results in decreased body weight gain and relative liver and kidney weight. Nickel treatment also resulted in alteration of hematological parameters along with increased liver and kidney toxicity markers. Nickel sulfate administration significantly increased the level of lipid peroxides and decreased antioxidant enzyme activities in hepatic and renal tissue. Simultaneous treatment with á-tocopherol exhibited a possible protective role on the toxic effect of nickel on body and organ weights, hematological parameters, SGPT activity and improved tissue antioxidant defense system. α-tocopherol, may partially prevent nickel induced alteration of hematological and biochemical parameters as well as have amelioratic effects on nickel induced alteration of antioxidant status of liver and kidney.
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Heavy metals are stable environmental contaminants, causing various alterations in target tissues. Garlic has some beneficial effect in preventing heavy metal induced various alteration. The objective was to investigate the possible protective role of fresh aqueous homogenate of garlic on hematology, erythrocyte antioxidant defense system in male albino rats treated with NiSO4 and K2Cr2O7. Rats were divided into six groups. Group I was untreated control. Group II was given aqueous homogenate of garlic (orally). Group III was administered with nickel sulfate (i.p). Group IV was given NiSO4 and garlic simultaneously. Group V was administered with K2Cr2O7 (i.p). Group VI were treated simultaneously with K2Cr2O7 and garlic. RBC, WBC, platelet count, PCV%, hemoglobin concentration decreased significantly and clotting time increased significantly after nickel treatment. After chromium treatment all the values decreased except clotting time. Increased malondialdehyde and glutathione level after nickel and chromium treatment was observed. Also erythrocyte superoxide dismutase, glutathione peroxidase and catalase activities significantly increased after nickel and chromium treatment. Simultaneous garlic supplementation exhibited protective role to combat nickel toxicity, whereas no such beneficial effects were observed for chromium (VI). Garlic may partially prevent nickel and chromium induced alteration but such ameliorated effects as an antioxidant is only restricted on nickel induced alteration.
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The present study was undertaken to establish short term memory status in Bipolar disorder cases as compared with normal age and sex matched control group in Bijapur (Karnataka). Results showed that a significant decrease in short term memory status in bipolar disorder cases as compared to their control group .Loss of attention, decreased processing speed and executive function patterns may be the probable causes of such observations.
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The optimal availability of immune cells in the peripheral blood stream of women plays a critical role in their response to disease and therapeutic interventions. Interaction between the reproductive and immune system plays an important immunoregulatory role. This study was designed to examine the impact of different phases of menstrual cycle on the blood leukocytes. Twenty-four healthy women in their reproductive age group and having regular menstrual cycle were studied during menstrual, proliferative and secretary phases of menstrual cycle. Total leukocyte count, absolute and differential counts of neutrophils, lymphocytes and mixed cells (includes eosinophils, basophils and monocytes) were analyzed. Results showed that the variations in the different types of leukocytes during different phases of menstrual cycle were not statistically significant. No significant inter group difference, except for the significant decrease in differential lymphocyte percentage in proliferative phase as compared to menses were observed.
Subject(s)
Adolescent , Female , Humans , Leukocyte Count , Menstrual Cycle/blood , Young AdultABSTRACT
This study aims to develop Peak Expiratory Flow Rate (PEFR) predictors for Karnataka Muslim male and female subjects of aged 18 to 20 years. PEFR was recorded in a standing position using mini Wright Peak Flow Meter on one hundred and four (104) healthy male and sixty one (61) healthy female subjects. Anthropometrical measurements i.e. height, weight, body surface area and body mass index were calculated. Statistically significant correlation were found in both sexes between PEFR and standing height (male, r = 0.94, P < 0.001; female, r = 0.95, P < 0.001), weight (male, r = 0.56, P < 0.001; female, r = 0.70, P < 0.001) and body surface area (male, r = 0.68, P < 0.001; female, r = 0.57, P < 0.001). The correlation between PEFR and body mass index were not found statistically significant in both sexes (male, r = 0.081; female, r = 0.17). The prediction equation for Karnataka male and female Muslim subjects (aged 18 to 20 years) based on height, weight and body surface area and multiple regression equation based on all those physical parameters have been developed (PEFR (l/m) (male) = 1.7304 x height + 0.155 x weight + 140.45 x BSA + 5.02; PEFR (l/m) (female) = 2.0448 x height--16.08 weight + 664.697 x BSA--101.24).