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1.
Scand J Pain ; 20(2): 215-227, 2020 04 28.
Article in English | MEDLINE | ID: mdl-31730537

ABSTRACT

Background and aims To systemically review the literature to compare freestyle lifting technique, by muscle activity and kinematics, between people with and without low back pain (LBP). Methods Five databases were searched along with manual searches of retrieved articles by a single reviewer. Studies were included if they compared a freestyle lifting activity between participants with and without LBP. Data were extracted by two reviewers, and studies were appraised using the CASP tool for case-control studies. Results Nine studies were eligible. Heterogeneity did not allow for meta-analysis. Most studies (n = 8 studies) reported that people with LBP lift differently to pain-free controls. Specifically, people with LBP lift more slowly (n = 6 studies), use their legs more than their back especially when initiating lifting (n = 3 studies), and jerk less during lifting (n = 1 studies). Furthermore, the four larger studies involving people with more severe LBP also showed that people with LBP lift with less spinal range of motion and greater trunk muscle activity for a longer period. Conclusions People with LBP move slower, stiffer, and with a deeper knee bend than pain-free people during freestyle lifting tasks. Interestingly, such a lifting style mirrors how people, with and without LBP, are often told how to lift during manual handling training. The cross-sectional nature of the comparisons does not allow for causation to be determined. Implications The changes described may show embodiment of cautious movement, and the drive to protect the back. There may be value in exploring whether adopting a lifting style closer to that of pain-free people could help reduce LBP.


Subject(s)
Lifting , Low Back Pain/physiopathology , Adult , Biomechanical Phenomena , Case-Control Studies , Cross-Sectional Studies , Female , Humans , Male , Middle Aged , Range of Motion, Articular
2.
Pediatr Surg Int ; 34(11): 1163-1169, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30132059

ABSTRACT

PURPOSE: Review current practices and expert opinions on contraindications to extracorporeal membrane oxygenation (ECMO) in congenital diaphragmatic hernia (CDH) and contraindications to repair of CDH following initiation of ECMO. METHODS: Modified Delphi method was employed to achieve consensus among members of the American Pediatric Surgical Association Critical Care Committee (APSA-CCC). RESULTS: Overall response rate was 81% including current and former members of the APSA-CCC. An average of 5-15 CDH repairs were reported annually per institution; 26-50% of patients required ECMO. 100% of respondents would not offer ECMO to a patient with a complex or unrepairable cardiac defects or lethal chromosomal abnormality; 94.1% would not in the setting of severe intracranial hemorrhage (ICH). 76.5% and 72.2% of respondents would not offer CDH repair to patients on ECMO with grade III-IV ICH or new diagnosis of lethal genetic or metabolic abnormalities, respectively. There was significant variability in whether or not to repair CDH if unable to wean from ECMO at 4-5 weeks. CONCLUSIONS: Significant variability in practice pattern and opinions exist regarding contraindications to ECMO and when to offer repair of CDH for patients on ECMO. Ongoing work to evaluate outcomes is needed to standardize management and minimize potentially futile interventions. LEVEL OF EVIDENCE: V (expert opinion).


Subject(s)
Extracorporeal Membrane Oxygenation , Hernias, Diaphragmatic, Congenital/surgery , Practice Patterns, Physicians' , Canada , Chromosome Aberrations , Contraindications , Contraindications, Procedure , Delphi Technique , Heart Defects, Congenital , Humans , Intracranial Hemorrhages , Medical Futility , Pediatrics , Surveys and Questionnaires , United States
4.
Bioorg Med Chem Lett ; 15(11): 2738-44, 2005 Jun 02.
Article in English | MEDLINE | ID: mdl-15878268

ABSTRACT

A new semicarbazone derivative of curcumin (CRSC) was synthesized and examined for its antioxidant, antiproliferative, and antiradical activity and compared with those of curcumin (CR). The antioxidant activity was tested by their ability to inhibit radiation induced lipid peroxidation in rat liver microsomes. The antiproliferative activity was tested by studying the in vitro activity of CRSC against estrogen dependant breast cancer cell line MCF-7. Kinetics of reaction of (2,2'-diphenyl-1-picrylhydrazide) DPPH, a stable hydrogen abstracting free radical was studied to measure the antiradical activity using stopped-flow spectrophotometer. Finally one-electron oxidized radicals of CRSC were generated and characterized by pulse radiolysis. The results suggest that the probable site of attack for CRSC is both the phenolic OH and the imine carbonyl position. CRSC shows efficient antioxidant and antiproliferative activity although its antiradical activity is less than that of CR.


Subject(s)
Antineoplastic Agents/pharmacology , Antioxidants/pharmacology , Cell Division/drug effects , Curcumin/pharmacology , Microsomes, Liver/drug effects , Semicarbazones/pharmacology , Animals , Cell Line, Tumor , Curcumin/chemistry , Drug Screening Assays, Antitumor , Gamma Rays , Humans , Lipid Peroxidation/drug effects , Rats , Semicarbazones/chemistry
5.
Cytometry A ; 62(2): 150-61, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15523603

ABSTRACT

BACKGROUND: Telomeres are specialized nucleoprotein structures at chromosome ends that undergo dynamic changes after each cell cycle. Understanding the mechanisms of telomere dynamics is critically dependent on the ability to accurately measure telomere length in a cell population of interest. Techniques such as Southern blot, which measures average telomere length, and quantitative fluorescence in situ hybridization (Q-FISH), which can estimate telomere length in individual chromosomes, are limited in their capacity to determine the distribution of cells with differing telomere lengths in a given cell population. METHODS: We employed flow-FISH to determine whether mouse and human cell lines exhibit subpopulations of cells with differing telomere lengths. RESULTS: Our analysis showed that at least one of four analyzed mouse cell lines had two subpopulations of cells with differing telomere lengths. Differences in telomere length between subpopulations of cells were significant, and we term this phenomenon TELEFLUCS (TElomere LEngth FLUctuations in Cell Subpopulations). We also observed TELEFLUCS in 1 of 19 analyzed human nonalternative lengthening of telomere cell lines and in 1 of 2 analyzed human alternative lengthening of telomere cell lines. The existence of cell subpopulations with differing telomere lengths was confirmed by Q-FISH. CONCLUSION: Our results underscore the importance of flow-FISH in telomere length analysis.


Subject(s)
Fibroblasts/cytology , Telomere , Animals , Cell Line, Tumor , Flow Cytometry , Humans , In Situ Hybridization, Fluorescence , Mice , Reverse Transcriptase Polymerase Chain Reaction , Telomerase/metabolism
6.
J Inorg Biochem ; 95(4): 306-14, 2003 Jul 01.
Article in English | MEDLINE | ID: mdl-12818801

ABSTRACT

The thiosemicarbazone derivative of 9,10-phenanthrenequinone, 1, and its metal complexes were synthesized. The X-ray crystal structure for 1 confirms the presence of the E tautomeric arrangement in this compound. Its copper complex shows 1:1 stoichiometry while nickel and cobalt compounds show 1:2 stoichiometry. The X-ray crystal structure of the nickel complex indicates two tridentate ligands coordinating in the thiolato form yielding an octahedral geometry for the 'mer' isomer. The copper complex exhibits maximum antiproliferative activity against human breast cancer cell-line, T47D probably due to inhibition of steroid binding to the cognitive receptor or by preventing dimerization of the estrogen receptor.


Subject(s)
Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/pharmacology , Breast Neoplasms/pathology , Metals/chemistry , Phenanthrenes/chemical synthesis , Phenanthrenes/pharmacology , Thiosemicarbazones/chemical synthesis , Thiosemicarbazones/pharmacology , Antineoplastic Agents/chemistry , Cell Division/drug effects , Cell Line, Tumor , Crystallography, X-Ray , Electrochemistry , Humans , Hydrogen Bonding , Magnetic Resonance Spectroscopy , Magnetics , Models, Molecular , Molecular Structure , Phenanthrenes/chemistry , Spectrum Analysis , Thiosemicarbazones/chemistry
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