Composers' Forum: Student Works, April 10, 1990

This is the concert program of the Composers' Forum: Student Works performance on Tuesday, April 10, 1990 at 12:30 p.m., at the Boston University Concert Hall, 855 Commonwealth Avenue, Boston, Massachusetts. Works performed were ME-A-RI by Nami Cho, Music Box by Juley B. Kurs, Control by Juley B. Kurs, Three Sketches for two pianos by Nami Cho, Preludes for piano by Juley B. Kurs, and Up and Down: Inner Rounds by John Saylor. Digitization for Boston University Concert Programs was supported by the Boston University Humanities Library Endowed Fund

NASA-Navy Telemedicine: Autogenic Feedback Training Exercises for Motion Sickness

Airsickness is the most significant medical condition affecting naval aviation training. A 2001 study showed that airsickness was reported in 81% of naval aviation students and was associated with 82% of below average flight scores. The cost to a single training air-wing was over $150,000 annually for fuel and maintenance costs alone. Resistent cases are sent to the Naval Aerospace Medical Institute (NAMI) for evaluation and desensitization in the self-paced airsickness desensitization (SPAD) program. This approach is 75$2,000 per student trained. 3. Reduce aviation training attrition. 4. Provide standardization of multi-location motion sickness training. 5. Future tri-service initiatives. 6. Data to NASA and Navy for QA and research opportunities

Searching transients in large-scale surveys. A method based on the Abbe value

(Abridged) A new method is presented to identify transient candidates in large-scale surveys based on the variability pattern in their light curves. The method is based on the Abbe value, that estimates the smoothness of a light curve, and on a newly introduced value called the excess Abbe that estimates the regularity of the light curve variability pattern over the duration of the observations. Based on simulated light curves, transients are shown to occupy a specific region in the Abbe versus Excess Abbe diagram, distinct from sources presenting pulsating-like features in their light curves or having featureless light curves. The method is tested on real light curves taken from EROS-2 and OGLE-II surveys in a 0.50deg x 0.17deg field of the sky in the LMC. The method identifies 43 EROS-2 transient candidates out of a total of ~1300 variable stars, and 19 more OGLE-II candidates. The efficiency of the method is further tested by comparing the list of transient candidates with known Be stars in the literature. It is shown that all Be stars known in the studied field of view with detectable bursts or outbursts are successfully extracted by the method. In addition, four new transient candidates displaying bursts and/or outbursts are found in the field, of which at least two are good new Be candidates. The new method proves to be a potentially powerful tool to extract transient candidates from large-scale multi-epoch surveys. The better the photometric measurement uncertainties are, the cleaner the list of detected transient candidates is. In addition, the diagram is shown to be a good diagnostic tool to check the data quality of multi-epoch photometric surveys. A trend of instrumental and/or data reduction origin, for example, will manifest itself by an unexpected distribution of points in the diagram.Comment: Accepted for publication in A&

Inhibition of endothelial cell functions and of angiogenesis by the metastasis inhibitor NAMI-A

NAMI-A is a ruthenium-based compound with selective anti-metastasis activity in experimental models of solid tumours. We studied whether this activity was dependent on anti-angiogenic ability of NAMI-A. We thus investigated its in vitro effects on endothelial cell functions necessary for angiogenesis to develop, as well as its in vivo effects in the chick embryo chorioallantoic membrane model. Endothelial cell proliferation, chemotaxis, and secretion of the matrix-degrading enzyme metalloproteinase-2 were inhibited by NAMI-A in a dose-dependent manner, and without morphologic signs of cell apoptosis or necrosis. Lastly, NAMI-A displayed a dose-dependent in vivo anti-angiogenic activity in the chorioallantoic membrane model. These data suggest that the anti-angiogenic activity of NAMI-A can contribute to its anti-metastatic efficacy in mice bearing malignant solid tumours

Antiangiogenic properties of selected ruthenium(III) complexes that are nitric oxide scavengers

The nitric oxide synthase (NOS) pathway has been clearly demonstrated to regulate angiogenesis. Increased levels of NO correlate with tumour growth and spreading in different experimental and human cancers. Drugs interfering with the NOS pathway may be useful in angiogenesis-dependent tumours. The aim of this study was to pharmacologically characterise certain ruthenium-based compounds, namely NAMI-A, KP1339, and RuEDTA, as potential NO scavengers to be used as antiangiogenic/antitumour agents. NAMI-A, KP1339 and RuEDTA were able to bind tightly and inactivate free NO in solution. Formation of ruthenium-NO adducts was documented by electronic absorption, FT-IR spectroscopy and (1)H-NMR. Pretreatment of rabbit aorta rings with NAMI-A, KP1339 or RuEDTA reduced endothelium-dependent vasorelaxation elicited by acetylcholine. This effect was reversed by 8-Br-cGMP. The key steps of angiogenesis, endothelial cell proliferation and migration stimulated by vascular endothelial growth factor (VEGF) or NO donor drugs, were blocked by NAMI-A, KP1339 and RuEDTA, these compounds being devoid of any cytotoxic activity. When tested in vivo, NAMI-A inhibited angiogenesis induced by VEGF. It is likely that the antitumour properties previously observed for ruthenium-based NO scavengers, such as NAMI-A, are related to their NO-related antiangiogenic propertie

Phefumula Nami

Cosmos: Building a cosmology (mid 17th century: from French cosmologie or modern Latin cosmologia, from Greek kosmos ‘order or world’ + -logia ‘discourse’,) which mirrors and exhumes hidden narratives from our current reality. It is in this tracing that I teeter between visual codes in the form of memories impressed upon my mind from generations of old and Aesthetic symphonies from the present

The hydrolysis mechanism of the anticancer ruthenium drugs NAMI-A and ICR investigated by DFT-PCM calculations

(ImH)[trans-RuCl4(DMSO-S)(Im)], (Im = imidazole, DMSO-S = S-bonded dimethylsulfoxide), NAMI-A, is the first anticancer ruthenium compound that successfully completed Phase I clinical trials. NAMI-A shows a remarkable activity against lung metastases of solid tumors, but is not effective in the reduction of primary cancer. The structurally similar (ImH)[trans-RuCl4(Im)(2)], ICR (or KP418), and its indazole analog (KP1019) are promising candidate drugs in the treatment of colorectal cancers, but have no antimetastatic activity. Despite the pharmacological relevance of these compounds, no rationale has been furnished to explain their markedly different activity. While the nature of the chemical species responsible for their antimetastatic/anticancer activity has not been determined, it has been suggested that the difference between reduction potentials of NAMI-A and ICR may be the key to the different biological responses they induce. In this work, Density Functional Theory calculations were performed to investigate the hydrolysis of NAMI-A and ICR in both Ru-III and Ru-II oxidation states, up to the third aquation. In line with experimental findings, our calculations provide a picture of the hydrolysis of NAMI-A and ICR mainly as a stepwise loss of chloride ligands. While dissociation of Im is unlikely under neutral conditions, that of DMSO becomes competitive with the loss of chloride ions as the hydrolysis proceeds. Redox properties of NAMI-A and ICR and of their most relevant hydrolytic intermediates were also studied in order to monitor the effects of biological reductants on the mechanism of action. Our findings may contribute to the identification of the active compounds that interact with biological targets, and to explain the different biological activity of NAMI-A and ICR

The Free Press Vol. 49, Issue No. 2, 09-18-2017

Superpower can’t protect it’s elderly -- 46th Student Senate holds first meeting -- USM Corporate Partners host panel discussion -- New program offers incentives for students -- NAMI on Campus joins Maine’s NAMI Walkhttps://digitalcommons.usm.maine.edu/free_press/1199/thumbnail.jp