Membrane Lipid Peroxidation Levels Research Articles

Effect of different concentrations of l-carnitine in extender for semen cryopreservation in sheep

This study assessed the effect of l-carnitine (LC) in sheep semen extenders containing or not egg yolk for cryopreservation in sheep. Two extenders (TRIS-egg yolk or the commercial optiXcell™ IMV medium) were used, totaling six groups: IMV – (0, 5 and 10 mM LC) and TRIS – (0, 5 and 10 mM LC). After the freezing-thawing process and throughout incubation at 38 °C for up to 3 h, several parameters were evaluated: sperm kinetics, hypoosmotic, plasma membrane integrity, capacitation status and lipid peroxidation level. The supplementation of either 5 or 10 mM LC randomly affected some parameters and, overall, TRIS was superior (P < 0.05) than IMV extender. In the LC-groups, IMV had greater (P < 0.05) oxidative stress than TRIS. In conclusion, although LC affected isolated parameters, its supplementation in semen extender had no consistently beneficial effect on freezing-thawing ram sperm.

Antioxidant Effects of Baoyuan Decoction on Dysfunctional Erythrocytes in High-Fat Diet-Induced Hyperlipidemic ApoE-/- Mice.

Baoyuan decoction (BYD), a traditional representative formula, has a long usage history in the treatment of cardiovascular diseases. Since the hyperlipidemia-induced dysfunction of erythrocyte is one of the most important causes of cardiovascular diseases, the improving effects of BYD against high-fat diet (HFD) induced the physiological and physical function of the erythrocytic injury and the potential mechanisms were deeply researched in this study. After 6 weeks of drug treatment, all doses of BYD had significantly decreased the lipid peroxidation in plasma of HFD-induced ApoE−/− mice, even if it had not improved the lipid levels. Then, the erythrocyte-related experimental results showed that BYD had reduced erythrocyte osmotic fragility, stabilized erythrocyte membrane skeleton protein 4.2, and reformed the erythrocyte morphological changes by decreasing erythrocyte membrane lipid peroxidation levels. This study demonstrated that BYD may ameliorate the physiological and physical function of erythrocyte in hyperlipidemic mice through the antioxidant effect on erythrocyte membranes.

Mitochondrial protective and antioxidant agents protect toxicity induced by depleted uranium in isolated human lymphocytes

Depleted uranium (DU) is a by-product of the enrichment procedure of natural uranium. During production and usage, uranium may be released into the environment due to failure to follow standard procedures, thus causing environmental pollution. In this study, toxicity effects of uranium (VI) and protective role of mitochondrial permeability transition pore sealing and antioxidant agents studied by isolated human lymphocytes. Human lymphocytes were exposed to different concentrations (0.1, 0.5, 1, 2 and 5 mM) of DU for 6 h and cytotoxicity was measured by trypan blue assay. The mechanistic parameters were assessed after 1, 2 and 3 h of lymphocyte treatment with 1/2 IC506h (0.3 mM), IC506h (0.8 mM) and 2 IC506h (1.6 mM) of DU. The reactive oxygen species (ROS), lysosomal membrane destabilization, mitochondrial membrane potential (MMP), lipid peroxidation, GSH and GSSG levels on human lymphocytes exposed to UA, were measured. The results indicate that toxicity of U (VI) was concentration dependent on human lymphocytes. Also, U (VI) induced ROS production, MMP reduction, lysosomal membrane destabilization and lipid peroxidation in human lymphocytes. In U (VI) treated lymphocytes, decrease in intracellular GSH and raise in extracellular GSSG levels were observed. We report that mitochondrial permeability transition (MPT) pore sealing and antioxidant agents, have the capacity significantly to prevents, mitochondrial toxicity. Thus, the inhibition of mitochondrial oxidative stress and mitochondrial dysfunction by MPT pore sealing and antioxidant agents is associated with the inhibition of DU-induced mitochondrial damages and activation of apoptosis in lymphocytes.

Effects of exogenous bisphenol A on the function of mitochondria in root cells of soybean (Glycine max L.) seedlings

Bisphenol A (BPA), a contaminant of emerging concern, can affect plant root growth by changing various physiological processes. Mitochondria are critical organelles that produce energy for growth. However, how BPA affects the function and ultrastructure of mitochondria and then plant root growth remains unclear. Here, we evaluated the lethality of BPA to root tip cells, investigated the energy production process of mitochondria, observed mitochondrial ultrastructure, and measured reactive oxygen species (ROS) and lipid peroxidation levels in mitochondria of soybean seedlings roots exposed to exogenous BPA. We found that low-dose BPA (1.5 mg/L) exposure induced limited toxicity in root tip cells, increased the activities of key enzymes (citrate synthase, succinate dehydrogenase, malate dehydrogenase and cytochrome C oxidase) involved in tricarboxylic acid cycle and oxidative phosphorylation, promoted adenosine triphosphate (ATP) synthesis, and increased ROS production in mitochondria. Higher doses of BPA (6.0, 17.2 mg/L) exposure caused massive cell death in root tips, decreased the above key enzyme activities and ATP production, and destroyed mitochondrial ultrastructure; meanwhile, these doses also significantly increased mitochondrial ROS and membrane lipid peroxidation levels. In conclusion, we found that mitochondria were significant subcellular sites through which BPA can damage plant roots. BPA-induced excessive ROS destroyed mitochondrial ultrastructure and inhibited key enzyme activities in energy production, resulting in decreased ATP synthesis and cell death in root tips. Our results demonstrated the effects of BPA on mitochondrial function and structure in plant root cells, providing new insights into understanding the underlying mechanisms of BPA affecting plant root growth.

The Investigation of the Antitumor Agent Toxicity and Capsaicin Effect on the Electron Transport Chain Enzymes, Catalase Activities and Lipid Peroxidation Levels in Lung, Heart and Brain Tissues of Rats.

Cisplatin is one of the most active cytotoxic agents in cancer treatment. To clarify the interaction with mitochondria, we hypothesize that the activities of mitochondrial electron transport chain (ETC) enzymes succinate dehydrogenase (SDH) and cytochrome c oxidase (COX), nucleotide levels, as well as levels of catalase (CAT) enzyme and membrane lipid peroxidation (LPO) can be affected by cisplatin. There was a significant decrease of both SDH and COX activities in the lung, heart, and brain tissues at the 1st day after cisplatin exposure, and the observed decreased levels of adenosine triphosphate (ATP) and adenosine diphosphate (ADP) in comparison with the control could be because of cisplatin-induced mitochondrial dysfunction. The investigations suggested that cisplatin inhibits SDH, COX, and ATP synthase. The higher LPO level in the studied tissues after 1 and 4 days post-exposure to cisplatin compared to control can be inferred to be a result of elevated electron leakage from the ETC, and reactive oxygen species (ROS) can lead to wide-ranging tissue damage such as membrane lipid damage. Consequently, it was observed that capsaicin may have a possible protective effect on ETC impairment caused by cisplatin. The activities of SDH and COX were higher in heart and brain exposed to cisplatin + capsaicin compared to cisplatin groups, while LPO levels were lower. The investigated results in the cisplatin + capsaicin groups suggested that the antioxidant capacity of capsaicin scavenges ROS and prevents membrane destruction.

Salicylic acid modulates cutting-induced physiological and biochemical responses to delay senescence in two gerbera cultivars

The postharvest longevity of gerbera (Gerbera jamesonii) flowers has a critical importance in determining their commercial value; and therefore, there is a commercial demand for prolonging their vase life (VL). Here, we tested the efficacy of salicylic acid (SA, 150 µM) preservative in extending longevity of cut flower of two gerbera cultivars, namely the ‘Sunway’ and ‘Bayadere’, of which water-held ‘Bayadere’ has longer VL than water-held ‘Sunway’. The results indicated that exogenous SA could significantly prolong the VL of cut flowers of both ‘Sunway’ and ‘Bayadere’ cultivars, with better preservative effect being observed on ‘Sunway’. SA preservative was more effective in ameliorating relative water uptake and relative fresh weight in ‘Sunway’ than in ‘Bayadere’, which was accompanied by a greater decrease in proline accumulation. Application of SA prolonged the VL of two cut gerbera flower cultivars by inhibiting the activity of polyphenol oxidase involved in browning reaction, and decreasing oxidative stress through improving reactive oxygen species-scavenging antioxidant capacity, which included accumulation of total phenolic compounds and total flavonoids, and enhancement of enzymatic antioxidant activities. As a result, membrane lipid peroxidation levels were reduced in cut flowers of both cultivars, with higher reduction level being observed in ‘Sunway’ than in ‘Bayadere’. Additionally, SA preservative was more efficient in maintaining a greater content of total soluble proteins in ‘Sunway’ than in ‘Bayadere’. These findings clearly demonstrated that SA has higher preservative effects on extending VL of ‘Sunway’ than that of ‘Bayadere’. Taken together, SA can be recommended to farmers for postharvest treatments to maintain quality and delay senescence of gerbera flowers.

Analysis of lipid peroxidation metabolism during florescence and senescence of Lily

In order to explore the correlation between the level of membrane lipid peroxidation and the physiological mechanism of senescence at different developmental stages of lily, the soluble protein content, soluble sugar content, malondialdehyde (MDA) content, superoxide radical (O2-) production rate, hydrogen peroxide (H2O2) content, superoxide dismutase (SOD) activity, catalase (CAT) activity, and peroxidase (POD) activity in petal of Lilium regale and Lilium leucanthum were measured at different developmental stages. The results showed that during flowering and senescence, soluble protein content in petal of L. regale changed with a single peak curve, while the content of soluble protein in petal of L. leucanthum decreased steadily. Soluble sugar content, SOD activity, and CAT activity of the two lilies increased first and then decreased. MDA content, H2O2 content,and O2- production rate continued to rise. POD activity of L. regale changed steadily, while POD activity of L. leucanthum increased significantly in the later stage. Therefore, the membrane lipid peroxidation caused by the accumulation of reactive oxygen species is one of the main physiological reasons for the senescence of lily.

ELABELA (ELA) Peptide Exerts Cardioprotection Against Myocardial Infarction by Targeting Oxidative Stress and the Improvement of Heart Function

Emerging evidence has shown that ELA peptide plays a pivotal role in cardiac development and modulation of vascular and cardiac function. In the current work, we sought to examine the possible therapeutic potential of ELA peptide to reduce I/R injury following MI and elucidate the possible mechanisms by which ELA peptide may ameliorate injury and improve heart function after MI. 5 µg/kg of ELA peptide was administrated intraperitoneally in rats once per day for 4 days after ischemia of heart for 30 min. Male Wistar rats were sacrificed at 24 h and 2 weeks after reperfusion. The infarct size was determined by TTC staining 2 weeks after reperfusion. ELISA was employed to measure serum level of myocardial injury markers such as LDH, CK-MB and Troponin I and oxidative stress markers such as membrane lipid peroxidation (MDA), GSH and SOD activities in the first 24 h. Cardiac function was evaluated using echocardiography prior to MI and 2 weeks after reperfusion. After administration of ELA peptide in MI rats, infarct size, serum levels of LDH, CK-MB, Troponin I and tissue levels of MDA were significantly reduced; GSH and SOD activities were markedly increased (p < 0.05). Likewise, ELA peptide improved cardiac function 2 weeks after MI (p < 0.05). ELA peptide administration for 4 days after MI could reduce injury by targeting oxidative stress and improvement of cardiac function. These findings establish a fundamental foundation for future peptide research and therapy.

Chloramine T induced oxidative stress and the response of antioxidant system in Phanerochaete chrysosporium.

In this study, the effect of chloramine T (Chl-T) on the activities of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), glutathione reductase (GR) and glutathione S-transferase (GST); the levels of reduced (GSH) and oxidised glutathione (GSSG) and their ratios; and also membrane lipid peroxidation (LPO) levels in Phanerochaete chrysosporium were investigated in a dose- (0.25-1mmol/L) and time-dependent (1.5-9h) manner. The highest SOD activity was observed in 0.5mmol/L Chl-T at 6th hour as 1.48-fold of its control. The observed highest level in CAT activities was 4.6-fold of control in 0.5 and 0.75mmol/L at the 6th hour. The GSH levels that were over the control showed decreasing tendency from the beginning of incubation, except 0.25mmol/L. In contrast with GSH level variations, GSSG levels reached 10.0-fold of its control by showing increasing tendency with the increases in concentration and time. While the GSH/GSSG ratios were over the control at 0.25mmol/L during all incubation, they fell under the control values at the earlier hours of incubation with the increasing concentrations of Chl-T. Glutathione-related enzymes GSH-Px, GR and GST were also induced with Chl-T treatment, and the highest activities were 3.29-, 7.5- and 6.56-fold of their controls, respectively. On the other hand, the increases in LPO levels with increasing concentration and time up to 5.27-fold of its control showed that the inductions observed in antioxidant system could not prevent the Chl-T-based oxidative stress.

Chlamydia trachomatis neither exerts deleterious effects on spermatozoa nor impairs male fertility

Chlamydia trachomatis is the most prevalent sexually transmitted bacterial infection. However, whether Chlamydia trachomatis has a negative impact on sperm quality and male fertility is still controversial. Herein, we report the effects on sperm quality of the in vitro exposure of spermatozoa to Chlamydia trachomatis, and also the effects of male genital infection on male fertility using an animal model. Human and mouse sperm were obtained from healthy donors and cauda epididimys from C57BL/6 mice, respectively. Highly motile human or mouse spermatozoa were in vitro exposed to C. trachomatis (serovar E or LGV) or C. muridarum, respectively. Then, sperm quality parameters were analyzed. Moreover, male fertility of Chlamydia muridarum infected male C57BL/6 mice was assessed. Human or murine sperm in vitro exposed to increasing bacterial concentrations or soluble factors from C. trachomatis or C. muridarum, respectively, did not show differences in sperm motility and viability, apoptosis, mitochondrial membrane potential, DNA fragmentation, ROS production and lipid peroxidation levels, when compared with control sperm (p > 0.05). Moreover, no differences in fertility parameters (potency, fecundity, fertility index, pre- and post-implantation loss) were observed between control and infected males. In conclusion, our results indicate that Chlamydia spp. neither directly exerts deleterious effects on spermatozoa nor impairs male fertility.

Responses of pomegranate cultivars to severe water stress and recovery: changes on antioxidant enzyme activities, gene expression patterns and water stress responsive metabolites.

The biochemical and molecular responses of five commercially well-known pomegranate cultivars to severe water stress were studied. The cultivars were subjected to 14-day water stress by withholding irrigation, followed by re-watering for 7days. Results showed clear differences in metabolites contents and activities of antioxidant enzymes among various pomegranate cultivars during severe water stress and recovery. According to our results, increased accumulation of proline in pomegranate was not related to osmotic adjustment during severe water stress. Except for 'Ghojagh', leaves grown under severe water stress conditions showed symptoms of oxidative stress such as reduced chlorophyll concentration. The improved performance of 'Ghojagh' under drought stress may be associated with an efficient osmotic adjustment. The up- or down regulated expression of cytosolic glutathione reductase (cytosolic GR) and glutathione peroxidase were observed under drought conditions. Moreover, the suppressed expression of cytosolic GR was also noted. Comparatively, 'Rabab' exhibited higher antioxidant capacity and an efficient ROS-scavenging mechanism under drought stress. Lower levels of membrane lipid peroxidation in 'Ghojagh' and 'Rabab' under drought stress and the marked reduction of malondialdehyde concentration after re-watering represents that these cultivars have a good tolerance to drought stress. As a first step towards the study of the biochemical and molecular responses of pomegranate plants to water stress, this research provides new information into the mechanisms of drought tolerance in the plants.

Ameliorative efficacy of quercetin against cisplatin‑induced mitochondrial dysfunction: Study on isolated rat liver mitochondria.

The present study aimed to investigate the hepatoprotective effects of the bioflavonoid quercetin (QR) on cisplatin (CP)‑induced mitochondrial oxidative stress in the livers of rats, to elucidate the role of mitochondria in CP‑induced hepatotoxicity, and its underlying mechanism. Isolated liver mitochondria were incubated with 100µg/ml CP and/or 50µM QR invitro. CP treatment triggered a significant increase in membrane lipid peroxidation (LPO) levels, protein carbonyl (PC) contents, and a decrease in reduced glutathione (GSH) and non‑protein thiol (NP‑SH) levels. In addition, CP caused a marked decline in the activities of enzymatic antioxidants and mitochondrial complexes (I, II, III and V) in liver mitochondria. QR pre‑treatment significantly modulated the activities of enzymatic antioxidants and mitochondrial complex enzymes. Furthermore, QR reversed the alterations in LPO and PC levels, and GSH and NP‑SH contents in liver mitochondria. The results of the present study suggested that QR supplementation may suppress CP‑induced mitochondrial toxicity during chemotherapy, and provides a potential prophylactic and defensive candidate for anticancer agent‑induced oxidative stress.

Fish oil protects rat erythrocytes against oxidative stress caused by Trypanosoma evansi infection

The effect of omega-3 polyunsaturated fatty acids has been the subject of intense study in many diseases; meanwhile, our understanding regarding the underlying mechanisms of omega-3 fatty acids against Trypanosoma evansi infection is still limited. A common feature of T. evansi infection is anemia. Erythrophagocytosis occurs due to direct traumatic actions of protozoa on the red blood cells, but the exact mechanisms of anemia are not yet fully understood. During infection, there is an increase in reactive oxygen species; some are highly toxic and rapidly detoxified by various cellular enzymatic and nonenzymatic mechanisms. For this purpose, the aim of this study was to evaluate the effect of fish oil (rich in omega-3) in protecting erythrocyte membranes from oxidative stress during experimental infection with T. evansi. For that, levels of membrane lipid peroxidation were analyzed and the activities of glutathione peroxidase (GPx), glutathione reductase, and catalase were also investigated. The level of lipid peroxidation increased in infected rats compared with the control, and differences were found in infected rats supplemented with fish oil 30 days before infection when compared with infected rats supplemented with fish oil after infection. Only the activity of GPx was changed in infected groups with a significantly reduced (p < 0.05) T. evansi-infected rats were treated for 30 days with fish oil (2 g/kg/day) before infection. The results suggest that the fish oil supplementation probably acts as a prophylactic treatment of T. evansi experimental infections in rats.

Erythrocyte Membrane Fluidity Alterations in Sudden Sensorineural Hearing Loss Patients: The Role of Oxidative Stress.

Introduction Sudden sensorineural hearing loss (SSNHL) involves an acute unexplained hearing loss, nearly always unilateral, that occurs over less than a 72-hour period. SSNHL pathogenesis is not yet fully understood. Cochlear vascular occlusion has been proposed as a potential mechanism of hearing damage and cochlear ischaemia has been related to alterations of cochlear microvessels. In addition, some researchers have focused their attention on the rheological alterations and blood hyperviscosity. Erythrocyte deformability plays a key role in determining blood viscosity, and it is critical to cochlear perfusion. It has been shown that oxidative stress-induced erythrocyte membrane fluidity alterations are linked to the progression of cardiovascular diseases. Methods To determine whether erythrocytes from SSNHL patients show signs of oxidative stress, and whether this condition can modify the haemorheologic profile in these patients, we analysed haemorheologic profile and erythrocyte oxidative stress in 35 SSNHL patients and 35 healthy subjects, matched for age and sex. Fluorescence anisotropy was used to evaluate the fluidity of erythrocyte membranes. Results Our results show a significant structural and functional involvement of erythrocyte membrane alterations in SSNHL, as well as elevated levels of membrane lipid peroxidation and intracellular reactive oxygen species (ROS) production. In addition, erythrocyte-derived ROS and erythrocyte lipid peroxidation positively correlated with whole blood viscosity and erythrocyte deformability. Moreover, in vitro experiments demonstrated that ROS display a key role in erythrocyte membrane fluidity. Conclusion These findings indicate that erythrocyte oxidative stress plays a key role in the pathogenesis of SSNHL and pave the way to new therapeutic interventions.

Mitochondria As the Target for the Modulatory Effect of Curcumin in Oxaliplatin-induced Toxicity in Isolated Rat Liver Mitochondria

To explore hepatoprotective action of curcumin (CMN, a bioflavonoid) on oxaliplatin (Oxa)-triggered mitochondrial oxidative stress and respiratory chain complexes in liver of rats. Oxa is a ubiquitously utilized platinum-based chemotherapeutic agent commonly used for the treatment of colorectal cancer. Mitochondria have recently emerged as targets for anticancer drugs in several kinds of toxicity including hepatotoxicity that can lead to neoplastic disease. There is a dearth of evidence involving the role of mitochondria in mediating Oxa-evoked hepatotoxicity and its underlying mechanism is still debatable. The study was performed in mitochondria isolated from liver of Wistar rats. Oxa (200μg/mL) and CMN (5μmol) were incubated under invitro conditions. Oxa evoked a significant increase in the membrane lipid peroxidation (LPO) levels, protein carbonyl (PC) contents, decrease in reduced glutathione (GSH) and nonprotein thiol (NP-SH) levels. Oxa also caused a marked decline in the activities of enzymatic antioxidants and respiratory chain enzymes (I, II, III and V) in liver mitochondria. CMN pre-treatment significantly prevented the activities of enzymatic antioxidants and mitochondrial respiratory chain enzymes. CMN also restored the LPO and PC contents, GSH and NP-SH levels in liver mitochondria. CMN intake might be effective in regulation of Oxa-evoked mitotoxicity during chemotherapy. Moreover, it is included in the armamentarium for anticancer agent-induced oxidative stress.

Oxidant and antioxidant status in Saccharomyces cerevisiae exposed to antifungal ketoconazole

Abstract In this study, production of intracellular reactive oxygen species (ROS) and nitric oxide (NO ),the activities of nicotinamide adenine dinucleotide (NADH) and nicotinamide adenine dinucleotide phosphate (NADPH) oxidases, superoxide dismutase (SOD) and catalase (CAT) and levels of membrane lipid peroxidation (LPO) in ketoconazole-treated Saccharomyces cerevisiae were investigated in a dose- and time-dependent manner. Hydrogen peroxide, total ROS and hydroxyl radical levels in 150–250 μM ketoconazole-treated cells were increased with increasing concentrations, which reached 4.30, 4.24 and 2.41 times their controls, respectively. Superoxide anion and NO radical levels increased dose-dependently up to the fourth hour and then dropped under the controls at 150–225 μM, while decreasing continuously at 250 μM. The highest levels were 2.23 and 3.43 times their controls, respectively. While NADH-NADPH oxidases and SOD activities increased with increasing time at 150–225 μM, extremely induced initial activities decreased throughout incubation at 250 μM. CAT activities were increased dose- and time-dependently up to the fourth hour and the activity reached 3.57 times the control. The highest LPO level was 2.28 times the control at 250 μM, because of the oxidative stress. The results showed that although the antioxidant system was effectively triggered, it couldn’t prevent S. cerevisiae from ketoconazole-induced oxidative stress.

Changes in chloroplast lipid contents and chloroplast ultrastructure in Sulla carnosa and Sulla coronaria leaves under salt stress

The possible involvement of chloroplast lipids in the mechanisms of NaCl tolerance was studied in leaves of two varieties of Fabaceae: Sulla carnosa and Sulla coronaria, which were subjected to 200mM NaCl over 20days. Changes in membrane lipid peroxidation, chloroplast lipids content, fatty acids (FA) composition and the ultrastructure of chloroplasts under salt stress were investigated. Chloroplast lipids were separated and quantified by high performance liquid chromatography coupled to evaporative light scattering detection (HPLC/ELSD). The results showed that salinity induced a significant decrease in digalactosyldiacylglycerol (DGDG), phosphatidylglycerol (PG) and sulfoquinovosylglycerol (SQDG) content in both S. carnosa and S. coronaria leaves, whereas monogalactosyldiacylglycerol (MGDG) content did not change significantly in S. carnosa leaves. The MGDG/DGDG ratio remained stable in S. coronaria leaves but increased in those of S. carnosa. In addition, the unsaturated-to-saturated fatty acids ratio (UFAs:SFAs) did not change under salt stress in S. coronaria leaves, while it decreased significantly in S. carnosa leaves. Moreover, salinity did not induce significant changes in MGDG and DGDG unsaturation level in S. carnosa leaves, in contrast to S. coronaria, in which salinity seems to enhance the unsaturation level in MGDG, DGDG and PG. Furthermore, the level of membrane lipid peroxidation, as expressed by malondialdehyde (MDA) levels, increased at 200mM in S. carnosa leaves, while it did not change significantly in those of S. coronaria. With respect to the ultrastructure of chloroplasts at 200mM NaCl, investigated by transmission electron microscopy (TEM), salt-stress caused the swelling of thylakoids in S. carnosa mesophyll. These ultrastructural changes were observed especially in the spongy tissue in S. coronaria. Taken together, these findings suggest that the stability of MGDG/DGDG ratio, the unchanged unsaturation level, and increasing unsaturation level in MGDG, DGDG and PG may be effective to some degree in suppressing the ultrastructural damage caused by salinity effects and may contribute to protect the chloroplast membrane integrity against salt stress.

Effects of UVB Radiation on the Physicochemical Properties of Fibroblasts and Keratinocytes.

The skin is the largest human organ, providing the first line of defense to protect the body from physical and environmental effects. The aim of this study was to determine the influence of short-wave ultraviolet (UVB) radiation on the membrane electrical properties, phospholipid content, and lipid peroxidation levels of fibroblasts and keratinocytes. Changes in cell function may affect the basal electrical surface properties of cell membranes. These changes can be detected using electrokinetic measurements. In this study, the surface charge densities of fibroblasts and keratinocytes were measured as a function of pH. A four-component equilibrium model was used to describe the interaction between the ions in solution and on cell membrane surfaces. Agreement was found between the experimental and theoretical charge variation curves of leukemia cells from pH 2.5 to pH 9. Phospholipid composition was determined qualitatively and quantitatively by HPLC, and lipid peroxidation was estimated by measuring the level of malondialdehyde. The acidic functional group concentrations and average association constants with hydroxyl ions were higher, and the average association constants with hydrogen ions were smaller in UVB-treated skin cell membranes compared to those in untreated cells. Moreover, our results showed that UVB radiation is associated with increased levels of phospholipids and lipid peroxidation products in fibroblasts and keratinocytes.

Effects of Adding Sodium Nitroprusside to Semen Diluents on Motility, Viability and Lipid Peroxidation of Sperm in Holstein Bulls.

Nitric oxide (NO) that plays important role in all sexual activities of animals is made from the amino acid L-arginine by the enzymatic action of NO synthase (NOS). NO makes a band with sulfur-iron complexes, but due to production of steroid sexual hormones related to the enzymes involved in this complex, NO can change the activity of these enzymes. NO affects many cells including vein endothelial cells, macrophages and mast cells. These cells are also found in Leydig cells; therefore, they are important source of NO in testis tissue. Therefore, minimizing damages to sperm at the time of freezing thawing process are really important. The aim of this study was to determine the appropriate NO concentration to be added to the freezing extender to improve the quality of thawed sperm. In this experimental randomized study, sperms of four Holstein bulls with an average age of 4 were collected twice a week for 3 weeks. They received sodium nitroprusside (SNP) in concentrations of 0, 10, 50 and 100 nmol/ml. Data analysis was performed using the special issue and static (SAS) 98 software. Also, mean comparison was done using Duncan's multiple ranges test (P<0.05).This research was conducted at the laboratory of Science and Research Branch, Islamic Azad University, Tehran at spring and summer of 2013. All concentrations of SNP used was found to increase motility and viability of spermatozoa at 1, 2 and 3 hours after thawing, significantly (P<0.05), but there was no significant difference at zero time. Different concentrations of SNP reduced the membrane lipid peroxidation level of sperm and increased acrosome membranes integrity, implying that SNP generally improved samples membranes, especially in 50 and 100 nmol/ml concentrations. According to the obtained results, addition of SNP to semen diluents increases motility and viability of spermatozoa. Also, it reduces membrane lipid peroxidation level that leads to improved sperm function.

Radioprotective Potential of Punica Granatum Extract and Synthetic Ellagic Acid: A Biochemical and Hematological Study in Mice

Radiation therapy has been used in cancer treatment for many decades; although effective in killing tumor cells, ROS produced in radiotherapy threaten the integrity and survival of surrounding normal cells. Recent studies have indicated that some commonly used medicinal plants may be good sources of potent but non-toxic radioprotectors. The pomegranate, Punica granatum L., an ancient, mystical, and highly distinctive fruit, is the predominant member of the Punicaceae family. It is used in several systems of medicine for a variety of ailments. The objective of the present study was to investigate the protective effects of ethanolic extracts of pomegranate whole fruit (EPWF) and Synthetic Ellagic acid (EA) against Electron beam radiation(EBR) induced biochemical and hematological alterations in Swiss albino mice. The extract and synthetic compound were assessed for its radical scavenging property by DPPH and FRAP assays. The animals were treated with 200mg/kg body wt. of pomegranate extract and Ellagic acid for 15 days before exposure to 6Gy of EBR. The hematological parameters were determined in the blood and biochemical estimations were carried out in the serumof sacrificed animals. The plant extract and synthetic compound exhibited good radical scavenging and reducing properties. The pretreated animals exhibited protective effect on the hematological parameters. Radiation induced depletion in the level of reduced glutathione and total antioxidant capacity were prevented significantly by EPWF and EA administration. Also there was significant reduction in the levels of membrane lipid peroxidation in the treated groups compared to irradiated control. The findings of our study indicate the protective efficacy of pomegranate extract and synthetic ellagic acid on radiation induced biochemical and hematological changes in mice may be due to its free radical scavenging and increased antioxidant levels.