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1.
Int J Oncol ; 51(3): 859-866, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28713989

ABSTRACT

Proton beam therapy has recently been used to improve local control of tumor growth and reduce side-effects by decreasing the global dose to normal tissue. However, the regulatory mechanisms underlying the physiological role of proton beam radiation are not well understood, and many studies are still being conducted regarding these mechanisms. To determine the effects of proton beams on mitochondrial biogenesis, we investigated: mitochondrial DNA (mtDNA) mass; the gene expression of mitochondrial transcription factors, functional regulators, and dynamic-related regulators; and the phosphorylation of the signaling molecules that participate in mitochondrial biogenesis. Both the mtDNA/nuclear DNA (nDNA) ratio and the mitochondria staining assays showed that proton beam irradiation increases mitochondrial biogenesis in 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced aggressive HT-29 cells. Simultaneously, proton beam irradiation increases the gene expression of the mitochondrial transcription factors PGC-1α, NRF1, ERRα, and mtTFA, the dynamic regulators DRP1, OPA1, TIMM44, and TOM40, and the functional regulators CytC, ATP5B and CPT1-α. Furthermore, proton beam irradiation increases the phosphorylation of AMPK, an important molecule involved in mitochondrial biogenesis that is an energy sensor and is regulated by the AMP/ATP ratio. Based on these findings, we suggest that proton beam irradiation inhibits metastatic potential by increasing mitochondrial biogenesis and function in TPA-induced aggressive HT-29 cells.


Subject(s)
Adenocarcinoma/radiotherapy , Colorectal Neoplasms/radiotherapy , DNA, Mitochondrial/radiation effects , Organelle Biogenesis , Adenocarcinoma/genetics , Adenocarcinoma/pathology , Adenosine Monophosphate/metabolism , Adenosine Monophosphate/radiation effects , Adenosine Triphosphate/metabolism , Adenosine Triphosphate/radiation effects , Colorectal Neoplasms/genetics , Colorectal Neoplasms/pathology , Gene Expression Regulation, Neoplastic/radiation effects , HT29 Cells , Humans , Neoplasm Proteins/radiation effects , Phosphorylation/radiation effects , Proton Therapy , Tetradecanoylphorbol Acetate/toxicity
2.
Crit Rev Eukaryot Gene Expr ; 22(3): 219-32, 2012.
Article in English | MEDLINE | ID: mdl-23140163

ABSTRACT

A state-of-the-art review of the role of the Langmuir-Blodgett nanotemplate on protein crystal structures is here presented. Crystals grown by nanostructured template appear more radiation resistant than the classical ones, even in the presence of a third-generation highly focused beam at the European Synchrotron Radiation Facility. The electron density maps and the changes in parameters such as total diffractive power, B-factor, and pairwise R-factor have been discussed. Protein crystals, grown by the Langmuir-Blodgett nanotemplate-based method, proved to be more radiation resistant compared to crystals grown by the classical hanging drop method in terms of both global and specific damage.


Subject(s)
Crystallization/methods , Nanostructures/chemistry , Nanotechnology/methods , Radiation , Adenosine Monophosphate/analogs & derivatives , Adenosine Monophosphate/chemistry , Adenosine Monophosphate/radiation effects , Dose-Response Relationship, Radiation , Models, Molecular , Proteins/chemistry , Proteins/radiation effects , Synchrotrons/instrumentation , Tetrahydrofolate Dehydrogenase/chemistry , Tetrahydrofolate Dehydrogenase/radiation effects
3.
J Chem Phys ; 128(7): 075102, 2008 Feb 21.
Article in English | MEDLINE | ID: mdl-18298174

ABSTRACT

We have studied the outcome of collisions between the hydrated nucleotide anion adenosine 5'-monophosphate (AMP) and sodium. Electron capture leads to hydrogen loss as well as water evaporation regardless of the initial number m of water molecules attached to the parent ion (m< or =16). The yield of dianions with microsecond lifetimes increases strongly with m, which is explained from dielectric screening of the two charges by the water nanodroplet. For comparison, collision induced dissociation results in water losses with no or very little damage of the AMP molecule itself.


Subject(s)
Adenosine Monophosphate/chemistry , Adenosine Monophosphate/radiation effects , Models, Chemical , Models, Molecular , Nanostructures/chemistry , Water/chemistry , Anions/radiation effects , Computer Simulation , Electrons , Nanostructures/radiation effects
4.
J Photochem Photobiol B ; 81(1): 26-32, 2005 Oct 03.
Article in English | MEDLINE | ID: mdl-16107316

ABSTRACT

In this work, the effects of visible (655 nm) and near-infrared (830 nm) light on ATP in solution were examined. The addition of irradiated ATP to the hexokinase reaction caused significant differences in the reaction rates and in the Michaelis-Menten kinetic parameters, k(m) and v(max). Irradiated ATP cleavage by hexokinase occurred in less time. Changes were wavelength and dose dependent. Excitation of ATP with a 260 nm wavelength ultraviolet light induced a fluorescence emission that was decreased when Mg2+ was added due to ion binding of the phosphates, which are the structures that modify the fluorescence produced by the adenine dipoles. The irradiation of this ATP.Mg2+ solution using 655 and 830 nm light increased the fluorescence by a possible displacement of Mg2+ from the phosphates. In conclusion, visible and near-infrared light modifies the biochemical behavior of ATP in the hexokinase reaction and the fluorescence intensity of the molecule thus altering the Mg2+ binding strength to the oxygen atoms in the phosphate group.


Subject(s)
Adenosine Triphosphate/radiation effects , Hexokinase/metabolism , Infrared Rays , Low-Level Light Therapy , Adenosine Diphosphate/radiation effects , Adenosine Monophosphate/radiation effects , Adenosine Triphosphate/metabolism , Fluorescence , Kinetics , Magnesium
5.
J Gravit Physiol ; 8(1): P41-2, 2001 Jul.
Article in English | MEDLINE | ID: mdl-12638616

ABSTRACT

It is known that plant resistance to stress factors is connected with energy metabolism. The energy stored in the process of photophosphorylation in the form of ATP is used then to support respiration, transpiration, organic compound synthesis, growth and development as well as to restore cell structure after its damage under extremal environmental factors. Transformation of light energy into chemical energy of ATP is catalyzed by thylakoid membrane enzymatic complex of ATPsynthase-CF1CF0. Its activity and amount in the thylakoid membrane depends on plant growth conditions. The aim of this work was investigation of clinorotation effect on light-induced dynamics of adenyl nucleotides (AMP, ADP and ATP) and estimation of CF1CF0 content in thylakoids of pea leaves grown under slow clinorotation and vertical control.


Subject(s)
Adenine Nucleotides/metabolism , Ca(2+) Mg(2+)-ATPase/metabolism , Light , Pisum sativum/metabolism , Rotation , Thylakoids/enzymology , Adenine Nucleotides/radiation effects , Adenosine Diphosphate/metabolism , Adenosine Diphosphate/radiation effects , Adenosine Monophosphate/metabolism , Adenosine Monophosphate/radiation effects , Adenosine Triphosphate/metabolism , Adenosine Triphosphate/radiation effects , Energy Metabolism , Pisum sativum/enzymology , Pisum sativum/radiation effects , Photophosphorylation/radiation effects , Plant Leaves/enzymology , Plant Leaves/metabolism , Plant Leaves/radiation effects , Thylakoids/metabolism , Thylakoids/radiation effects , Time Factors , Weightlessness Simulation
6.
Adv Space Res ; 15(3): 131-4, 1995 Mar.
Article in English | MEDLINE | ID: mdl-11539214

ABSTRACT

We have investigated in detail radiation and thermal stabilities and transformations of adenosine mono- and triphosphates in liquid and frozen solid aqueous solutions within a wide range of absorbed radiation dose (up to 75 kGy) and temperature (up to 160 degrees C). Dephosphorylation is the main pathway of high temperature hydrolysis of adenine nucleotides. Basic thermodynamic and kinetic parameters of this process have been determined. Radiolysis of investigated compounds at room temperature results in scission of N-glycosidic bond with a radiation yield about of 1 mol/100 eV. Solution freezing significantly enhances radiation stability of nucleotides as well as other biomolecules. This circumstance is essential in the discussion of panspermia concepts.


Subject(s)
Adenine Nucleotides/chemistry , Adenosine Monophosphate/radiation effects , Adenosine Triphosphate/radiation effects , Evolution, Chemical , Gamma Rays , Adenine Nucleotides/radiation effects , Adenosine Monophosphate/chemistry , Adenosine Triphosphate/chemistry , Chromatography, High Pressure Liquid , Chromatography, Thin Layer , Hot Temperature , Hydrogen-Ion Concentration , Hydrolysis , Radiochemistry
7.
Radiol Med ; 87(6): 837-46, 1994 Jun.
Article in English | MEDLINE | ID: mdl-7518933

ABSTRACT

The role of AMP was investigated in radiosensitization by the use of prochlorperazine in normal rat skin. AMP metabolism was evaluated by estimating the level of activities of 5' nucleotidase vis-à-vis protein, DNA and RNA contents in prochlorperazine-treated plus irradiated skin. To study radiation-induced changes in the skin, the extent of lipid peroxidation was measured in terms of enzyme lipid peroxidase. After irradiation, lipid peroxidase activity was observed to increase in prochlorperazine-treated rat skin. Subsequently the level of 5' nucleotidase was found to decrease in drug-treated plus irradiation skin. Similarly, the suppression in the levels of DNA, RNA and protein contents increased when the rat skins was irradiated in the presence of sensitizer prochlorperazine. The cytological examination, which revealed the extent of the lesions occurring in the normal rat skin, and the biochemical examination demonstrated increased cellular lethality in prochlorperazine-sensitized skin after irradiation. The results suggest that prochlorperazine probably sensitizes the normal skin tissues to radiation by inhibiting AMP metabolism via hydroxy-radical-induced decrease in DNA, RNA and protein metabolism.


Subject(s)
Adenosine Monophosphate/radiation effects , Prochlorperazine/pharmacology , Radiation-Sensitizing Agents/pharmacology , Skin/drug effects , Skin/radiation effects , 5'-Nucleotidase/drug effects , 5'-Nucleotidase/metabolism , 5'-Nucleotidase/radiation effects , Adenosine Monophosphate/metabolism , Animals , DNA/drug effects , DNA/metabolism , DNA/radiation effects , Lipid Peroxidation/drug effects , Lipid Peroxidation/radiation effects , Male , Protein Biosynthesis , Proteins/drug effects , Proteins/radiation effects , RNA/drug effects , RNA/metabolism , RNA/radiation effects , Rats , Rats, Inbred Strains , Skin/metabolism , Skin/pathology , Time Factors
8.
Med Pr ; 45(3): 201-7, 1994.
Article in Polish | MEDLINE | ID: mdl-8084258

ABSTRACT

The authors studied the effect of gamma radiation and submaximum physical exercise on adenosine-5'-triphosphate (ATP), adenosine-5'-diphosphate (ADP) and adenosine-5'-monophosphate (AMP) contents in erythrocytes of healthy males. Twenty one men aged 20-22 years were examined. They underwent physical exercise at doses of 2 w/kg body weight for 15 min. Erythrocytes were exposed to gamma radiation (500 gy doses) from 60Co source. The concentration of adenine nucleotides in erythrocytes was measured by the Boehringer Mannheim tests. The submaximum physical exercise was found to decrease ATP content and to to increase ADP and AMP in erythrocytes. Gamma radiation at 500 Gy dose was found to decrease ATP concentration in erythrocytes both at rest and after submaximum exercise and to increase AD content. It was revealed that AMP content increased at rest and decreased after submaximum exercise in irradiated erythrocytes.


Subject(s)
Adenosine Diphosphate/radiation effects , Adenosine Monophosphate/radiation effects , Adenosine Triphosphate/radiation effects , Erythrocytes/radiation effects , Gamma Rays , Physical Exertion/physiology , Adenosine Diphosphate/metabolism , Adenosine Monophosphate/metabolism , Adenosine Triphosphate/metabolism , Adult , Erythrocytes/metabolism , Humans , Male , Reference Values
9.
Eur J Biochem ; 179(2): 435-40, 1989 Feb 01.
Article in English | MEDLINE | ID: mdl-2917573

ABSTRACT

N6-(N-[(4-Azido-3,5,6-trifluoro)pyridin-2-yl]-2-aminoethyl)- adenosine 5'-monophosphate has been synthesized and evidence presented for its structural assignment by ultraviolet and 19F-NMR spectroscopies. Its photolysis was shown to occur within 5 min. This AMP derivative behaves as a competitive inhibitor of NAD+ in horse-liver-alcohol-dehydrogenase-promoted oxidation of ethanol, with a Ki (0.95 mM) comparable to the Ki of AMP (1.9 mM). Moreover it is an activator of the enzyme when nicotinamide ribose is used as the oxidation cofactor. This activation is as good as that promoted by AMP or by the well known 8-azido-AMP. Upon photolysis of this new derivative in the presence of horse liver alcohol dehydrogenase, a covalent enzyme--analogue complex was isolated and assayed as a catalyst in the oxidation of ethanol using nicotinamide ribose as the cofactor. The reaction took place without complementation of AMP, indicating clearly that the AMP analogue is mainly covalently bound in the AMP-binding site, and that the linkage formed between the enzyme and the azido derivative has not dramatically altered the active site of the enzyme. A similar experiment with 8-azido-AMP produced a completely inactive complex.


Subject(s)
Adenosine Monophosphate/analogs & derivatives , Alcohol Dehydrogenase/metabolism , Azides/chemical synthesis , Liver/enzymology , Adenosine Monophosphate/chemical synthesis , Adenosine Monophosphate/pharmacology , Adenosine Monophosphate/radiation effects , Alcohol Dehydrogenase/radiation effects , Animals , Azides/pharmacology , Azides/radiation effects , Binding Sites , Binding, Competitive , Catalysis , Magnetic Resonance Spectroscopy , Molecular Structure , NAD/antagonists & inhibitors , Oxidation-Reduction/drug effects , Photochemistry , Photolysis , Spectrophotometry, Ultraviolet
10.
Radiat Res ; 113(3): 447-57, 1988 Mar.
Article in English | MEDLINE | ID: mdl-3347702

ABSTRACT

The formation of (R)- and (S)-8,5'-cycloadenosine 5'-monophosphate (8,5'-cycloAMP), 8-hydroxyadenosine 5'-monophosphate (8-hydroxyAMP), and radiolytic adenine release from irradiated solutions of adenosine 5'-monophosphate (5'-AMP) was measured as a function of increasing liquid-phase oxygen concentration. Three classes of specific molecular damage were identified on the basis of the oxygen dependence for product formation. Major changes in product yield occurred near the range of oxygen concentrations associated with the radiobiological oxygen effect. In addition to these data, systematic increases in the concentration of hydrogen peroxide at the time of irradiation resulted in an increase in the yield of 8-hydroxyAMP and a component of radiolytic adenine release in nitrogen-saturated solutions of 5'-AMP. However, no changes in the yield of the 8,5'-cyclonucleotides were observed under these conditions.


Subject(s)
Adenosine Monophosphate/radiation effects , Oxygen , Adenine/analysis , Adenosine Monophosphate/analogs & derivatives , Adenosine Monophosphate/analysis , Cobalt Radioisotopes , Gamma Rays , Solutions
11.
Article in English | MEDLINE | ID: mdl-2984127

ABSTRACT

This survey focuses on recent developments in the radiation chemistry of purine bases in nucleic acids and related model compounds. Both direct and indirect effects of ionizing radiation are investigated with special emphasis on the structural characterization of the final decomposition products of nucleic acid components. Available assays for monitoring radiation-induced base lesions are critically reviewed.


Subject(s)
DNA/radiation effects , Purines/radiation effects , Adenine/radiation effects , Adenosine Monophosphate/radiation effects , Deoxyadenosines/radiation effects , Deoxyguanosine/radiation effects , Electron Spin Resonance Spectroscopy , Free Radicals , Hydroxides , Radiochemistry
12.
Radiat Res ; 97(1): 97-107, 1984 Jan.
Article in English | MEDLINE | ID: mdl-6695047

ABSTRACT

DNA repair has been investigated, estimated by unscheduled DNA synthesis (UDS) and the cellular NAD+ pool, after exposing human mononuclear leukocytes to hyperthermia and gamma radiation separately and in combination. It was found that gamma radiation induced a decline in UDS with increasing temperature through the temperature region studied (37-45 degrees C). At 42.5 degrees C the gamma-ray-induced UDS was reduced to about 70% of that at 37 degrees C. Following gamma-ray damage the NAD+ pool dropped to about 20% of control values. Without hyperthermic treatment the cells completely recovered to the original level within 5 hr. Moderate hyperthermia (42.5 degrees C for 45 min) followed by gamma-ray damage altered the kinetics so that even after 8 hr the NAD+ pool had recovered to only 70% of the original level. After heat treatment at 44 degrees C for 45 min prior to gamma radiation the cells did not recover at all, presumably because of the cytotoxic effects from the combined treatment.


Subject(s)
DNA Repair/radiation effects , DNA/radiation effects , Hyperthermia, Induced , Monocytes/radiation effects , NAD/radiation effects , Adenosine Diphosphate/metabolism , Adenosine Diphosphate/radiation effects , Adenosine Monophosphate/metabolism , Adenosine Monophosphate/radiation effects , Adenosine Triphosphate/metabolism , Adenosine Triphosphate/radiation effects , Cell Survival/radiation effects , Cells, Cultured , DNA/biosynthesis , Gamma Rays , Humans , Monocytes/metabolism , NAD/metabolism , Time Factors
13.
Biofizika ; 26(3): 394-7, 1981.
Article in Russian | MEDLINE | ID: mdl-7260149

ABSTRACT

Effect of UV-irradiation on non-aqueous solutions of adenine nucleotide mixture of the presence of inorganic phosphate was studied. Solutions of ADP sodium salts containing AMP and ATP admixtures and of inorganic phosphate in DMSO and DMPA and ethylene glycol were illuminated with the lamp dPIII-500. It has been shown that along with nucleotide disintegration and complex formation ATP synthesis takes place, which is evidenced by an increase of relative ATP content in experimental specimens.


Subject(s)
Adenosine Triphosphate/radiation effects , Ultraviolet Rays , Adenosine Diphosphate/radiation effects , Adenosine Monophosphate/radiation effects , Kinetics , Mathematics , Phosphates
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