Macroscopic and microscopical investigations of the effects of alcoholic extract of henna (Lawsonia inermis) on skin healing of experimentally induced tissue damage in macro fish (Labidochromis caeruleus)

One of the well-known herbal drugs is henna (Lawsonia inermis). According to the components in henna, several beneficial properties (i.e., antimicrobial, anti-inflammation, wound healing, trypsin inhibitory and antioxidant) have been reported. The present study was designed to investigate the effects of two natural substances (sodium chloride and henna extract) on experimental skin lesion due to pulling out scales and trypsin injection (0/02 ml, beneath dorsal fin). For this purpose, 54 fish in weight 5/5±0/55 of were divided to 3 groups, with eighteen fish in each group. Fishes were placed in laboratory condition in 22-25 ˚C. Two, four and six days after induction of skin injury, fishes were treated with different agents for 10 minutes. First group was treated in salt water 1%, second group in henna extract 0.5% and the control group without any additives. The fish were sampled weekly, 3 times by sampling from the wound. Macroscopic examination showed that color changes of wound place decreased in henna group in comparison with that other groups. In third week of healing, normal appearance of skin were seen in most of fishes in henna and salt groups. Microscopic study revealed a decrease in inflammatory cells infiltration in henna group second week after induction of skin injury. It seems that henna by decreasing inflammatory process, can also prevent skin damage and secondary infections that can help faster and more effective on wound healing than salt bath in fish

Combination therapy with pulse cyclophosphamide plus corticosteroids improves renal outcome in patients with lupus nephritis

Background: The prognosis of SLE is influenced by the onset of glomerulonephritis. Clinical trials in lupus nephritis have demonstrated that cyclophosphamide therapy is the superior regimen in the management of lupus nephritis for preserving renal function. Objective: The purpose of this study is to define the outcome of renal function with bolus pulses of cyclophosphamide and steroid according to our protocol and also to determine an appropriate pattern of treatment of lupus nephritis. Methods: In this open-label clinical trial, to evaluate the results, the short-term prognosis and the rate of complications of an immunosuppressive regimen with corticosteroids and cyclophosphamide, twenty-five patients with biopsy-proven lupus nephritis were studied. Treatment was structured in 4 phases: 1) Induction with bolus methylprednisolone and cyclophosphamide. 2) Maintenance with oral prednisolone for 4 weeks and monthly cyclophosphamide pulses for 6 months. 3) Tapering with reduction of prednisolone by 10 each month and continuing cyclophosphamide every other month till one year and for the second year every 3 months. 4) Discontinuation with oral prednisolone slowly tapered to the least effective daily dose and cyclophosphamide discontinued after 2 yr of therapy. We defined primary outcome measures according to these criteria: renal function return to normal limits or become stable, regression of systemic and local inflammatory symptoms, urine protein excretion falling below 0.3 gr/dL or by at least 50, RBC cast disappearance, C3, C4, Hb, and ESR return to normal limits. Results: Twenty-three patients with lupus nephritis completed our therapeutic protocol. Renal biopsy was performed in 22 cases and indicated type IV in 20 patients (95.2), and type V in 2 patients. After an average of 4+1.95 months 22 patients achieved remission (95.65) and only one case remained non-responsive. She became pregnant in her fourth month of therapy. Significant statistical differences were achieved between creatinine, proteinuria, hematuria, leukocyturia, urinary cast, C3, C4, ESR, and Hb before and after therapy (p<0.05). Plasma creatinine fell from 1.44+0.95 mg/dL to 0.97+0.78 (p<0.004). Proteinuria fell from 1879.78+1854.46 to 408.34+572.92 mg/24h (p<0.001). Thirteen episode of relapses were treated again with repeated cycles of cyclophosphamide and all remitted again. Conclusion: Intensive immunosuppression with steroid and cyclophosphamide provides excellent results with an acceptable rate of complications in the treatment of lupus nephritis

Compensatory growth assessment by plasma IGF-I hormone measurement and growth performance in rainbow trout (Oncorhynchus mykiss)

This study aimed to show the difference in compensatory growth (CG) with different starvation and feeding periods replications, depending on the IGF-I hormone level in the blood. There were 4 treatments in 3 replications. Other indexes like food coefficient ratio (FCR), specific growth rate (SGR) and daily food intake were also examined during the experiment. Fish were fed twice a day ad libitum as follows during the 65 days. Treatment A (TA): control treatment, continues feeding. Treatment B (TB): 4 weeks of starvation and 5 weeks of re-feeding. Treatment C (TC): 3 weeks of starvation and 5 weeks of re-feeding. Treatment D (TD): 2 weeks of starvation and 5 weeks of re-feeding. Each tank contained 23fishes in each unit with an initial mean weight (SD) of 47.19 &#177; 0.42 (g). Blood was sampled in IGF-I hormone concentration at the beginning of the experiment, at the end of the starvation period and every 12 days in re-feeding periods. There was no significant difference between the treatments in FCR (P &gt; 0.05). TB and TC had significant difference (P &lt; 0.01) in comparison with other treatments in SGR, but no significant difference was observed among them (P &gt; 0.05). IGF-I concentrations came down in comparison with control treatment at the end of the starvation period (Day 29) (P &lt; 0.001), but no significant difference was observed among the treatments at the end of the re-feeding period (P &gt; 0.05). According to the results, TB and TC showed more indexes of CG in comparison with TA and TD. Still IGF-I cannot show the quality of CG alone and other growth relating physiological elements in different feeding diets and regimes will be evaluated in future studies

Glial cells are functionally impaired in juvenile neuronal ceroid lipofuscinosis and detrimental to neurons.

The neuronal ceroid lipofuscinoses (NCLs or Batten disease) are a group of inherited, fatal neurodegenerative disorders of childhood. In these disorders, glial (microglial and astrocyte) activation typically occurs early in disease progression and predicts where neuron loss subsequently occurs. We have found that in the most common juvenile form of NCL (CLN3 disease or JNCL) this glial response is less pronounced in both mouse models and human autopsy material, with the morphological transformation of both astrocytes and microglia severely attenuated or delayed. To investigate their properties, we isolated glia and neurons from Cln3-deficient mice and studied their basic biology in culture. Upon stimulation, both Cln3-deficient astrocytes and microglia also showed an attenuated ability to transform morphologically, and an altered protein secretion profile. These defects were more pronounced in astrocytes, including the reduced secretion of a range of neuroprotective factors, mitogens, chemokines and cytokines, in addition to impaired calcium signalling and glutamate clearance. Cln3-deficient neurons also displayed an abnormal organization of their neurites. Most importantly, using a co-culture system, Cln3-deficient astrocytes and microglia had a negative impact on the survival and morphology of both Cln3-deficient and wildtype neurons, but these effects were largely reversed by growing mutant neurons with healthy glia. These data provide evidence that CLN3 disease astrocytes are functionally compromised. Together with microglia, they may play an active role in neuron loss in this disorder and can be considered as potential targets for therapeutic interventions

The introduction and refinement of the assessment of digitally recorded audio presentations

This case study critically evaluates benefits and challenges of a form of assessment included in a final year undergraduate Religious Studies Open University module, which combines a written essay task with a digital audio recording of a short oral presentation. Based on the analysis of student and tutor feedback and sample assignments, this study critically examines how teaching and learning practices linked to this novel form of assessment have been iteratively developed in light of the project findings over a period of two years. It concludes that while this form of assessment poses a number of challenges, it can create valuable opportunities for the development of transferable twenty-first-century graduate employability skills as well as deep, effective learning experiences, particularly – though not exclusively – in distance learning settings

Glass is a viable substrate for precision force microscopy of membrane proteins

Scientific Reports ; 5:12550 ; DOI: 10.1038/srep12550.Chada, N. et al. Glass is a Viable Substrate for Precision Force Microscopy of Membrane Proteins. Sci. Rep. 5, 12550; doi: 10.1038/srep12550 (2015).8 pages.Received: 01 April 2015 ; Accepted: 02 July 2015 ; Published: 31 July 2015.Though ubiquitous in optical microscopy, glass has long been overlooked as a specimen supporting surface for high resolution atomic force microscopy (AFM) investigations due to its roughness. Using bacteriorhodopsin from Halobacterium salinarum and the translocon SecYEG from Escherichia coli, we demonstrate that faithful images of 2D crystalline and non-crystalline membrane proteins in lipid bilayers can be obtained on microscope cover glass following a straight-forward cleaning procedure. Direct comparison between AFM data obtained on glass and on mica substrates show no major differences in image fidelity. Repeated association of the ATPase SecA with the cytoplasmic protrusion of SecYEG demonstrates that the translocon remains competent for binding after tens of minutes of continuous AFM imaging. This opens the door for precision long-timescale investigations of the active translocase in near-native conditions and, more generally, for integration of high resolution biological AFM with many powerful optical techniques that require non-birefringent substrates.Includes bibliographical references

Evaluation of mRNA expression levels of cyp51a and mdr1, candidate genes for voriconazole resistance in Aspergillus flavus

Background: Voriconazole Resistance (VRC-R) in Aspergillus flavus isolates impacts the management of aspergillosis, since azoles are the first choice for prophylaxis and therapy. However, to the best of our knowledge, the mechanisms underlying voriconazole resistance are poorly understood. Objectives: The present study was designed to evaluate mRNA expression levels of cyp51A and mdr1 genes in voriconazole resistant A. flavus by a Real-Time Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) technique. Materials and Methods: Five A. flavus isolates with resistance to VRC were examined by a RT-PCR approach. Results: Four out of five isolates revealed cyp51A and mdr1 mRNA overexpression. Interestingly, the isolate, which was negative for cyp51A and mdr1 mRNA expression showed a high voriconazole Minimum Inhibitory Concentration (MIC). Furthermore, a computational-based analysis predicted that voriconazole resistance could be mediated through cooperation with a network protein interaction. Conclusions: Our experimental and in silico findings may provide new insight in the complex molecular pathways of drug resistance and also could assist design an efficient therapeutic strategy for aspergillosis treatment. © 2015 Ahvaz Jundishapur University of Medical Sciences

Expression of efflux pumps and fatty acid activator one genes in azole resistant Candida glabrata isolated from immunocompromised patients

Acquired azole resistance in opportunistic fungi causes severe clinical problems in immunosuppressed individuals. This study investigated the molecular mechanisms of azole resistance in clinical isolates of Candida glabrata. Six unmatched strains were obtained from an epidemiological survey of candidiasis in immunocompromised hosts that included azole and amphotericin B susceptible and azole resistant clinical isolates. Candida glabrata CBS 138 was used as reference strain. Antifungal susceptibility testing of clinical isolates was evaluated using Clinical and Laboratory Standards Institute (CLSI) methods. Complementary DNA-Amplified Fragment Length Polymorphism (cDNA-AFLP) technology, semiquantitative RT-PCR, and sequencing were employed for identification of potential genes involved in azole resistance. Candida glabrata Candida drug resistance 1 (CgCDR1) and Candida glabrata Candida drug resistance 2 (CgCDR2) genes, which encode for multidrug transporters, were found to be upregulated in azole-resistant isolates (�2-fold). Fatty acid activator 1 (FAA1) gene, belonging to Acyl-CoA synthetases, showed expression in resistant isolates �2-fold that of the susceptible isolates and the reference strain. This study revealed overexpression of the CgCDR1, CgCDR2, and FAA1 genes affecting biological pathways, small hydrophobic compounds transport, and lipid metabolism in the resistant clinical C.glabrata isolates. © 2016 Tehran University of Medical Sciences. All rights reserved