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1.
Nanoscale ; 7(26): 11263-6, 2015 Jul 14.
Article in English | MEDLINE | ID: mdl-26067629

ABSTRACT

The water-insolubility of a potentially versatile photoresponsive 'turn-on' fluorescence probe was overcome by incorporating it into a nano-assembly containing an upconverting nanoparticle wrapped in an amphiphilic polymer. The appeal of the nano-system is not only in the ability to turn "on" and "off" the fluorescence from the organic chromophore using UV and visible light, it is in the fact that the nanoparticle acts as a static probe because it emits red and green light when excited by near infrared light, which is not effected by UV and visible light. This dual-functioning emission behaviour was demonstrated in live organisms.


Subject(s)
Caenorhabditis elegans/metabolism , Fluorescent Dyes , Nanoparticles/chemistry , Optical Imaging , Ultraviolet Rays , Animals , Caenorhabditis elegans/cytology , Fluorescent Dyes/chemistry , Fluorescent Dyes/pharmacology
3.
Ecotoxicology ; 21(2): 439-55, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22037694

ABSTRACT

Caenorhabditis elegans strains carrying stress-reporter green fluorescent protein transgenes were used to explore patterns of response to metals. Multiple stress pathways were induced at high doses by most metals tested, including members of the heat shock, oxidative stress, metallothionein (mtl) and xenobiotic response gene families. A mathematical model (to be published separately) of the gene regulatory circuit controlling mtl production predicted that chemically similar divalent metals (classic inducers) should show additive effects on mtl gene induction, whereas chemically dissimilar metals should show interference. These predictions were verified experimentally; thus cadmium and mercury showed additive effects, whereas ferric iron (a weak inducer) significantly reduced the effect of mercury. We applied a similar battery of tests to diluted samples of soil pore water extracted centrifugally after mixing 20% w/w ultrapure water with air-dried soil from an abandoned lead/zinc mine in the Murcia region of Spain. In addition, metal contents of both soil and soil pore water were determined by ICP-MS, and simplified mixtures of soluble metal salts were tested at equivalent final concentrations. The effects of extracted soil pore water (after tenfold dilution) were closely mimicked by mixtures of its principal component ions, and even by the single most prevalent contaminant (zinc) alone, though other metals modulated its effects both positively and negatively. In general, mixtures containing similar (divalent) metal ions exhibited mainly additive effects, whereas admixture of dissimilar (e.g. trivalent) ions often resulted in interference, reducing overall levels of stress-gene induction. These findings were also consistent with model predictions.


Subject(s)
Biosensing Techniques/methods , Caenorhabditis elegans/drug effects , Environmental Monitoring/methods , Metals/toxicity , Soil Pollutants/toxicity , Soil/chemistry , Animals , Caenorhabditis elegans/genetics , Caenorhabditis elegans/physiology , Caenorhabditis elegans Proteins/genetics , Caenorhabditis elegans Proteins/metabolism , Drug Interactions , Groundwater/chemistry , Metallothionein/genetics , Metallothionein/metabolism , Metals/analysis , Models, Biological , Organisms, Genetically Modified , Oxidative Stress/drug effects , Soil Pollutants/analysis , Up-Regulation/drug effects
4.
J Am Chem Soc ; 131(44): 15966-7, 2009 Nov 11.
Article in English | MEDLINE | ID: mdl-19810719

ABSTRACT

Using light to modulate biochemical agents in living organisms has a significant impact on photodynamic therapy and drug release. We demonstrate that a photoresponsive system can reversibly induce paralysis in nematodes as a model for living organisms when two different wavelengths of light are used to toggle the molecular switch between its two structural forms. This example illustrates how photoswitches offer great potential for advancing biomedical technologies.


Subject(s)
Ethylenes/radiation effects , Light , Paralysis/drug therapy , Animals , Caenorhabditis elegans/drug effects , Cyclization/radiation effects , Ethylenes/pharmacology , Models, Animal , Photochemotherapy/methods
5.
Hum Mol Genet ; 18(21): 4089-101, 2009 Nov 01.
Article in English | MEDLINE | ID: mdl-19648295

ABSTRACT

Duchenne Muscular Dystrophy is an inherited muscle degeneration disease for which there is still no efficient treatment. However, compounds active on the disease may already exist among approved drugs but are difficult to identify in the absence of cellular models. We used the Caenorhabditis elegans animal model to screen a collection of 1000 already approved compounds. Two of the most active hits obtained were methazolamide and dichlorphenamide, carbonic anhydrase inhibitors widely used in human therapy. In C. elegans, these drugs were shown to interact with CAH-4, a putative carbonic anhydrase. The therapeutic efficacy of these compounds was further validated in long-term experiments on mdx mice, the mouse model of Duchenne Muscular Dystrophy. Mice were treated for 120 days with food containing methazolamide or dichlorphenamide at two doses each. Musculus tibialis anterior and diaphragm muscles were histologically analyzed and isometric muscle force was measured in M. extensor digitorum longus. Both substances increased the tetanic muscle force in the treated M. extensor digitorum longus muscle group, dichlorphenamide increased the force significantly by 30%, but both drugs failed to increase resistance of muscle fibres to eccentric contractions. Histological analysis revealed a reduction of centrally nucleated fibers in M. tibialis anterior and diaphragm in the treated groups. These studies further demonstrated that a C. elegans-based screen coupled with a mouse model validation strategy can lead to the identification of potential pharmacological agents for rare diseases.


Subject(s)
Carbonic Anhydrase Inhibitors/pharmacology , Disease Models, Animal , Dystrophin/deficiency , Muscular Dystrophy, Animal/prevention & control , Animals , Caenorhabditis elegans/drug effects , Caenorhabditis elegans/genetics , Caenorhabditis elegans/physiology , Caenorhabditis elegans Proteins/genetics , Caenorhabditis elegans Proteins/metabolism , Carbonic Anhydrase Inhibitors/metabolism , Carbonic Anhydrases/genetics , Carbonic Anhydrases/metabolism , Dichlorphenamide/pharmacology , Dose-Response Relationship, Drug , Drug Evaluation, Preclinical , Dystrophin/genetics , Humans , Methazolamide/pharmacology , Mice , Mice, Inbred mdx , Motor Activity , Muscle Contraction/drug effects , Muscle, Skeletal/drug effects , Muscle, Skeletal/pathology , Muscle, Skeletal/physiopathology , Muscular Dystrophy, Animal/genetics , Muscular Dystrophy, Animal/physiopathology , RNA Interference , Time Factors
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