RESUMO
At pH values 5 and 9, the influence of cysteine, cystine, 3-mercaptopropionic acid and S-methylcysteine on the induction of H-adduct radicals in thymidine and thymidine 5'-monophosphate photosensitized by proflavin is investigated. The results obtained indicate that efficient protection is given when the electrostatic interactions between the charged groups of the molecules present allow the close proximity of a thiol or a disulfide bridge and the proflavin - DNAs complex constituent. The scheme proposed for the mechanism involves the capture by the protector of an electron or a proton, indispensable intermediates in the formation of the H-adduct radicals.
Assuntos
Acridinas , Proflavina , Compostos de Sulfidrila , Timidina , Nucleotídeos de Timina , Fenômenos Químicos , Química , Dissulfetos , Espectroscopia de Ressonância de Spin Eletrônica , Radicais Livres , Concentração de Íons de Hidrogênio , Conformação Molecular , FotoquímicaRESUMO
Frozen aqueous solutions of thymine and its derivatives were irradiated with visible light (lambda greater than 320 nm) in the presence of various furocoumarins. ESR analysis revealed the induction of hydrogen adduct free radicals at C-6 position of thymine, only with those furocoumarin derivatives which show a skin-photosensitizing ability. It has been shown, moreover, that the photocycloaddition of psoralen to thymine, which is responsible for the biological effects of this dye, is inhibited when the induction of free radicals in thymine moiety has been prevented by electron scavengers. It is suggested that the free radicals observed could be involved in the biological photosensitization. The mechanism of free radical generation and singlet oxygen production by furoccoumarins were also investigated.
Assuntos
Cumarínicos/farmacologia , Timidina Monofosfato/efeitos da radiação , Timidina/efeitos da radiação , Nucleotídeos de Timina/efeitos da radiação , Timina/efeitos da radiação , Espectroscopia de Ressonância de Spin Eletrônica , Transferência de Energia , Radicais Livres , Luz , OxigênioRESUMO
It is shown that the insertion of nucleotides between proflavine molecules is favourable to photosensitization. Furthermore (1) each molecule of proflavine gives at the most one free radical in the substrate, (2) the chromophore is largely restored when oxygen is not present, (3) superoxide radicals are observed in the presence of oxygen, and (4) formyl radicals are detected. The scheme elaborated for the mechanism gives an explanation for all these observations.
Assuntos
Acridinas , Desoxirribonucleotídeos , Proflavina , Sítios de Ligação , Espectroscopia de Ressonância de Spin Eletrônica , Radicais Livres , Congelamento , Concentração de Íons de Hidrogênio , Conformação Molecular , Conformação de Ácido Nucleico , Fotoquímica , ÁguaRESUMO
Bacteriophage phi X174 single-stranded DNA molecules were primed with five different restriction fragments and irradiated with visible light in the presence of proflavine. This photodamaged DNA was used as template for the in vitro complementary chain synthesis by E. coli DNA polymerase I (Klenow fragment). Chain terminations were observed by polyacrylamide gel electrophoresis of the synthesized products and localized by comparison with standard sequencing performed simultaneously on the untreated template. 90% of the chain terminations occurred one nucleotide before a guanine residue in the template strand. More than 80% of the sequenced guanine residues were blocking lesions demonstrating the absence of 'hot-spots' for the photodamaging effect of proflavine. At a defined position, the chain termination frequency increased linearly with the irradiation time and was directly influenced by the proflavine concentration present. An important part of lesions resulted from the action of singlet oxygen produced by excited proflavine as shown by the effect that both NaN3 and 2H2O exerted on the reaction. The induced blocking lesions must be important in vivo since no complete replicative forms could be extracted from cell infected with bacteriophages inactivated by 'proflavine and light' treatment.
Assuntos
Acridinas/farmacologia , Bacteriófago phi X 174/genética , Replicação do DNA/efeitos dos fármacos , DNA de Cadeia Simples/genética , Proflavina/farmacologia , Bacteriófago phi X 174/efeitos dos fármacos , Bacteriófago phi X 174/efeitos da radiação , Sequência de Bases , DNA Polimerase I/metabolismo , Replicação do DNA/efeitos da radiação , Escherichia coli/enzimologia , Luz , FotóliseRESUMO
Analysis of the bacteriochlorin a absorption spectra suggests the existence of a monomer-dimer equilibrium, particularly intense in phosphate buffer and favored by a decrease of the pH. The dye in methanolic solution is predominantly in monomeric form. Fluorescence and electron spin resonance nitroxide spin labeling measurements indicate that incorporation into the lipid phase of dimyristoyl-L-alpha-phosphatidylcholine liposomes induces dye monomerization. Moreover, the molecules are bound in the external surface of the vesicles and a complete incorporation is ensured by a lipid-to-dye ratio greater than 125.
Assuntos
Fármacos Fotossensibilizantes/química , Porfirinas/química , Dimerização , Dimiristoilfosfatidilcolina , Espectroscopia de Ressonância de Spin Eletrônica , Concentração de Íons de Hidrogênio , Lipossomos , Substâncias Macromoleculares , Membranas Artificiais , Conformação Molecular , Soluções , Espectrometria de Fluorescência , EspectrofotometriaRESUMO
Bacteriophage M13 mp10 DNA were irradiated with near-UV light in the presence of tetracycline derivatives and primed with synthetic oligonucleotide to be used for DNA synthesis using Escherichia coli DNA polymerase. Chain terminations were observed by denaturing polyacrylamide gel electrophoresis and mapped precisely. All the synthesis stops occurred before or at the level of guanine residues, showing that the photoreaction mediated by tetracycline derivatives led to a preferential alteration of guanine residues. These lesions were demonstrated to be induced in DNA through a pathway involving singlet oxygen. Tetracycline derivatives also photoinduced the breakage of the DNA sugar-phosphate backbone monitored by the conversion of supercoiled phi X174 DNA to a relaxed form. This lesion was shown to be initiated by hydroxyl radicals. The production of this free radical has been confirmed by electron paramagnetic resonance (EPR) spin trapping experiments using 5,5-dimethyl-1-pyrroline-N-oxide as spin trap. In addition to the EPR signal due to OH radicals trapping another unassigned signal has been detected.
Assuntos
DNA/efeitos da radiação , Tetraciclina/farmacologia , Animais , DNA de Cadeia Simples/efeitos da radiação , Espectroscopia de Ressonância de Spin Eletrônica , Transtornos de FotossensibilidadeRESUMO
This survey focuses on recent developments in the field of the ultraviolet photochemistry and photobiology of phenothiazine derivatives. One of the major alterations introduced by this kind of photosensitized reaction is a covalent addition of the photosensitizer or one of its photoproducts onto the macromolecular target. This reaction has been observed with soluble and membrane proteins, lipids and DNA. In the latter case, the addition occurs at the level of guanine residues and leads to inhibition of DNA replication.
Assuntos
Fenotiazinas , Raios Ultravioleta , Animais , Proteínas Sanguíneas/metabolismo , Clorpromazina/metabolismo , DNA/metabolismo , DNA/efeitos da radiação , Radicais Livres , Lipídeos/efeitos da radiação , Proteínas de Membrana/efeitos da radiação , Oxigênio , Fenotiazinas/metabolismo , Fotoquímica , Fotólise , Promazina/metabolismo , Proteínas/efeitos da radiação , Oxigênio Singlete , Soluções , SuperóxidosRESUMO
Promazine derivatives induce cross-linking of bovine lens crystallins in vitro by irradiation with near-ultraviolet (UV) light in the presence of O2, as revealed by electrophoresis after denaturation. With the five derivatives tested (promazine [PZ], chlorpromazine [CPZ], triflupromazine [ TFPZ ], methoxypromazine [ MTPZ ], and acepromazine [ ACPZ ] ), single-hit kinetics are observed. Evidence implicating the cation radicals of the PZ derivatives as the causative agent of this in vitro effect is presented. Hydroxyl radicals do not appear to be involved in the photo-cross-linking reaction. Sodium ascorbate protects against damage induced either by PZ derivatives plus light or by PZ cation radicals in the dark. These findings are discussed with respect to development of cataracts induced by these drugs in vivo.
Assuntos
Cristalinas/metabolismo , Cristalino/efeitos dos fármacos , Promazina/farmacologia , Acepromazina/farmacologia , Animais , Bovinos , Clorpromazina/farmacologia , Cristalinas/efeitos da radiação , Radicais Livres/metabolismo , Técnicas In Vitro , Oxigênio/metabolismo , Fenotiazinas/farmacologia , Triflupromazina/farmacologia , Raios UltravioletaRESUMO
An important aspect of the infection by the human immunodeficiency virus (HIV-1) type 1 is its clinical latency, suggesting that the virus itself or the provirus may remain latent for extended periods of time after primary infection. Certain heterologous viral proteins or chemical and physical agents are able to reactivate latent virus. Since a common denominator shared by these agents is the ability to cause stress response in cells, we have examined the effects of oxidative stress mediated by hydrogen peroxide (H2O2) on HIV-1 latently infected promonocytic cell line termed U1. After exposure to H2O2 in concentrations ranging from 0.1 to 2 mM, the viability of the U1 cells decreased during 24 h before recovery. At 24 h post stress, the U1 cells began to express virus as assessed by elevated reverse transcriptase activities in culture supernatants. Immunofluorescence carried out on stressed U1 cells using anti-HIV-1 polyclonal antibodies showed that H2O2 leads to HIV-1 gene expression activation, but not to a release of viral particles from damaged cells. Additionally, using a HeLa cell line containing integrated the bacterial chloramphenicol acetyl transferase (CAT) gene under the control of the HIV-1 long terminal repeat (LTR), we have shown that oxidative stress mediated by H2O2 allows transactivation of the viral LTR revealed by intracellular CAT activity. A stimulation factor of around 4 of CAT activity can be reached when these cells are treated with 0.5 mM H2O2.(ABSTRACT TRUNCATED AT 250 WORDS)
Assuntos
HIV-1/crescimento & desenvolvimento , Peróxido de Hidrogênio/farmacologia , Ativação Viral , Divisão Celular , Linhagem Celular , Sobrevivência Celular , Imunofluorescência , Regulação Viral da Expressão Gênica , Repetição Terminal Longa de HIV , HIV-1/genética , Células HeLa , Humanos , Cinética , Ativação Linfocitária , Monócitos/imunologia , Neutrófilos/imunologia , OxirreduçãoRESUMO
Superhelical pBR322 DNA has been photosensitized in the presence of various promazine derivatives. Agarose gel electrophoresis of the photosensitized DNA reveals that true single-strand breaks are induced during irradiation. Alkaline treatment of the photosensitized DNA with a subsequent alkaline agarose gel electrophoresis demonstrates that in addition to true single-strand breaks, these drugs can induce alkali-labile lesions. Although true single-strand breaks are induced randomly into a 5'-[32P]-end labeled pBR322 DNA fragments, the alkaline-labile alterations are located specifically at the level of guanine residues. A strong correlation seems to exist between the visualization of this labilization and the induction of a covalent photoadduct on guanine by the photosensitization mediated by PZ.
Assuntos
DNA/efeitos dos fármacos , Promazina/farmacologia , Álcalis , DNA/efeitos da radiação , Dano ao DNA , Eletroforese em Gel de Ágar , Eletroforese em Gel de PoliacrilamidaRESUMO
Promazine derivatives are known to be able to photoinduce, in vitro, direct single-strand breaks into DNA (Decuyper et al., Biochem. Pharmac. 33, 4025-4031 (1984]. Using [32P]end labeled DNA fragments, it is demonstrated that this DNA breakage occurs almost regardless of the nucleotide sequence of the DNA. Using 3'-[32P]end or 5'-[32P]end labeled oligonucleotide and enzymatic digestion of the fragments generated, it is demonstrated that the termini generated at the site of the breakage are 5'-phosphate, 3'-phosphate and 3'-termini which are presumed to be 3'-phosphoglycolate. This is consistent with an attack of the sugar moeity of the sugar-phosphate backbone of the DNA by the reactives species generated upon near-u.v. irradiation of promazine derivatives.
Assuntos
DNA/efeitos da radiação , Promazina/farmacologia , Eletroforese em Gel de Poliacrilamida , Raios gama , Hidróxidos , Radical Hidroxila , Monoéster Fosfórico Hidrolases/farmacologia , FotoquímicaRESUMO
In vitro transcription by E. coli RNA polymerase was carried out on SV40 DNA photoreacted with various promazine derivatives. Inhibition of the template activity was recorded with increasing irradiation times in the presence of promazine derivatives. Promazine covalent adducts on guanine did not terminate RNA synthesis and seemed to be bypassed by the enzyme. HMT (4'-hydroxymethyl-4,5',8-trimethylpsoralen) photoreaction with DNA was carried out under two conditions: irradiation with lambda greater than 395 nm favouring monoadduction on pyrimidine residues and irradiation at 360 nm inducing a maximum of interstrand diadducts. Both adducts were able to terminate RNA synthesis on the phototreated SV40 DNA and using the O-methyl-nucleotide sequencing procedure, the termination sites were precisely mapped. Monoadducts on the coding strand and cross-links induced termination two bases away from the covalent adduct, but monoadducts on the noncoding strand did not half RNA polymerase.
Assuntos
DNA Viral/efeitos dos fármacos , Furocumarinas/farmacologia , Promazina/análogos & derivados , Promazina/farmacologia , Vírus 40 dos Símios/genética , Trioxsaleno/farmacologia , Sequência de Bases , DNA Viral/efeitos da radiação , RNA Polimerases Dirigidas por DNA/metabolismo , Escherichia coli/enzimologia , Cinética , Relação Estrutura-Atividade , Transcrição Gênica/efeitos dos fármacos , Transcrição Gênica/efeitos da radiação , Trioxsaleno/análogos & derivadosRESUMO
Near-u.v. photoexcited promazine and three of its derivatives are shown to induce single-strand breaks in phi X174-DNA replicative form. The mechanisms of this DNA breakage depend upon the various photochemical properties of the promazine derivatives. Chlorpromazine is shown to act predominantly via the photodechlorination reaction both in aerobic and anaerobic conditions. The three other promazine derivatives (promazine, trifluopromazine and methoxypromazine) display two mechanisms for DNA breakage. One of them occurs through the cation radical, which is formed during near-u.v. irradiation of promazine derivatives. The second mechanism is demonstrated to act via an hydroxyl radical-dependent pathway. Acepromazine is without photoactivated action. EPR-spin-trapping studies of irradiated mixtures, containing the drugs and 5,5-dimethyl-1-pyrroline-N-oxide (as spin trap), suggest the production of superoxide radical by photoexcited promazines. When DNA is present in the irradiation mixture, this superoxide radical is converted into hydroxyl radical probably via a Haber Weiss-type reaction, catalysed by DNA-iron complexes.
Assuntos
DNA , Luz , Promazina/toxicidade , Espectroscopia de Ressonância de Spin Eletrônica , Radicais Livres , Hidróxidos , Radical Hidroxila , Fotólise , Promazina/análogos & derivados , SuperóxidosRESUMO
Monomers and aggregates of Merocyanine 540 (MC540) in water are able to photoisomerize. The shape of the photoisomer absorption spectrum is very similar to that of the ground state. Triplet state of MC540 in water has been produced by energy transfer from triplet anthracene and displays a broad absorption spectrum between 600 and 700 nm. The triplet state may also be produced by direct excitation of MC540 with UV light. However, when the dye is excited by visible light, no triplet state absorbance in the red could be detected so that the triplet yield of MC540 in water seems to be excitation wavelength dependent.
Assuntos
Pirimidinonas/química , Radiossensibilizantes/química , Cinética , Fotólise , ÁguaRESUMO
The quantum yield of singlet oxygen production by eight newly synthesized sulfur and selenium analogs of psoralen irradiated with UV-A (366 nm) has been determined in CCl4 with the help of the steady state luminescence technique. The new psoralen derivatives are generally better singlet oxygen producers than psoralen itself. In particular, the replacement of selenophene for furan and/or of thiopyrone for pyrone induces an important enhancement of the singlet oxygen quantum yield.
Assuntos
Furocumarinas/efeitos da radiação , Oxigênio , Raios Ultravioleta , Furocumarinas/química , Fotoquímica , Teoria Quântica , Oxigênio Singlete , Espectrofotometria Ultravioleta , Relação Estrutura-AtividadeRESUMO
Photodynamic therapy with bacteriochlorin a (BCA) as sensitizer induces damage to red blood cells in vivo. To assess the extent of the contributuion of reactive oxygen species (ROS) and to determine a possible reaction mechanism, competition experiments with assorted ROS quenching or/and enhancing agents were performed in human erythrocytes as model system and in phosphate buffer. In the erythrocyte experiments, a 2% suspension was incubated with BCA for 1 h, washed with phosphate-buffered saline, resuspended and subsequently illuminated with a diode laser using a fluence rate of 2.65 mW/cm2. Potassium leakage and hemolysis were light and BCA dose dependent. Adding tryptophan (3.3 mM), azide (1 mM) or histidine (10 mM) to the erythrocyte suspension before illumination delayed the onset of K-leakage and hemolysis suggesting a type II mechanism. The D2O did not affect K-leakage nor photohemolysis. Adding mannitol (13.3 mM) or glycerol (300 nM) also caused a delay in the onset of K-leakage and hemolysis, suggesting the involvement of radicals. In phosphate buffer experiments, it was shown using electron spin resonance (ESR) associated with spin-trapping techniques that BCA is able to generate O2-. and OH. radicals without production of aqueous electron. Visible or UV irradiation of the dye in the presence of the spin trap 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) gave an ESR spectrum characteristic of the DMPO-hydroxyl radical spin adduct DMPO-OH. Addition of ethanol or sodium formate produced supplementary hyperfine splittings due to the respective CH3CHOH. and CO2-. radical adducts, indicating the presence of free OH.. Production of DMPO-OH was partly inhibited by superoxide dismutase (SOD), catalase and desferrioxamine, suggesting that the iron-catalyzed decomposition of H2O2 was partly involved in the formation of one part of the observed OH.. The complementary inhibition of DMPO-OH production by azide and 9,10-anthracenedipropionic acid (ADPA) was consistent with 1O2 production by BCA followed by reaction of 1O2 with DMPO and decay of the intermediate complex to form DMPO-OH and free OH.. All our results seem to indicate that BCA is a 50%/50% type 1/type 2 sensitizer in buffered aqueous solutions and confirmed that the dye-induced hemolysis of erythrocytes was cell caused by a mixed type 1/type 2 mechanism.
Assuntos
Eritrócitos/metabolismo , Eritrócitos/efeitos da radiação , Óxidos N-Cíclicos , Espectroscopia de Ressonância de Spin Eletrônica , Eritrócitos/efeitos dos fármacos , Hemólise/efeitos dos fármacos , Hemólise/efeitos da radiação , Humanos , Radical Hidroxila/sangue , Técnicas In Vitro , Oxigênio/sangue , Fotoquimioterapia/efeitos adversos , Fármacos Fotossensibilizantes/toxicidade , Porfirinas/toxicidade , Oxigênio Singlete , Marcadores de Spin , Superóxidos/sangueRESUMO
The effect of the ingestion of the carcinogenic substance DAB on the density and distribution of organic free radicals in rat liver is studied by the electron spin resonance method. There is a remarkable parallelism between what is known about the evolution of the activity of mitochondria and the concentration variations of free radicals.
Assuntos
Fígado/efeitos dos fármacos , p-Dimetilaminoazobenzeno/farmacologia , Animais , Espectroscopia de Ressonância de Spin Eletrônica , Radicais Livres , Masculino , Mitocôndrias Hepáticas/efeitos dos fármacos , Neoplasias/análise , RatosRESUMO
Irradiation in the presence of O2, with near-UV light of five promazine (PZ) derivatives added to erythrocyte ghost membranes, causes covalent cross-linking between proteins as revealed by a progressive decrease in the amounts of proteins separable by electrophoresis after denaturation. The induction of cross-links in the two spectrin subunits is a single-hit process as a function of the irradiation time; relatively the rate constants (in min-1) of the photoreactions were 0.060 with chlorpromazine (CPZ), 0.039 with methoxypromazine (MTPZ), 0.031 with PZ, 0.029 with triflupromazine (TFPZ) and 0.006 with acepromazine (ACPZ). A main photochemical intermediate implicated in the spectrin aggregation seems to be the cation radical of the PZ derivatives. Indeed, (i) the chemically generated cation radicals can induce the reaction in the dark; (ii) the photoaggregation is regularly reduced upon addition of increasing concentrations of NaN3; (iii) NaN3 similarly affects the amount of cross-links induced by the isolated cation radicals. Hydroxyl radicals are also involved in the photocross-linking when the reaction is initiated only by MTPZ and not by the other sensitizers. In the absence of oxygen during irradiation, PZ, MTPZ and ACPZ completely loose their cross-linking activities whereas CPZ and TFPZ remain as efficient as in the presence of oxygen.
Assuntos
Proteínas de Membrana/metabolismo , Fenotiazinas/toxicidade , Raios Ultravioleta , Animais , Azidas/farmacologia , Membrana Eritrocítica/efeitos dos fármacos , Membrana Eritrocítica/efeitos da radiação , Radicais Livres , Nitrogênio/farmacologia , Fotoquímica , OvinosRESUMO
Inactivation of øX174 bacteriophages as a function of the irradiation time in the near-UV and in the presence of triflupromazine (TFPZ), promazine (PZ), chlorpromazine (CPZ) or methoxypromazine (MTPZ) proceeds according to single hit kinetics. Acepromazine (ACPZ) has no significant activity. At low concentrations (0.1 mM) TFPZ and PZ are the most active compounds. Higher concentrations (up to 5 mM) result in a protective effect by these two compounds but cause increased inactivation rates in the case of MTPZ or CPZ. Photoinactivation mediated by TFPZ or CPZ increases the reversion frequency of a øXamber mutant. Neither MTPZ nor PZ sensitization induces mutagenesis. The effect of NaN3 on the phage inactivation rate varies depending upon both the sensitizer and the concentration of the quencher. Phage inactivation in an N2 atmosphere is measurable only in the presence of high concentrations of CPZ and MTPZ. The drugs do not show any selectivity for calf thymus DNA or bovine serum albumin, at least as measured by dialysis equilibrium experiments.
Assuntos
Bacteriófago phi X 174/efeitos dos fármacos , Mutagênicos , Fenotiazinas/toxicidade , Raios Ultravioleta , Azidas/farmacologia , Bacteriófago phi X 174/genética , Bacteriófago phi X 174/efeitos da radiação , DNA/metabolismo , Mutação , Nitrogênio/farmacologia , Fotoquímica , Soroalbumina Bovina/metabolismoRESUMO
The induction of sister-chromatid exchanges (SCE) together with the proliferation rate index (PRI) were studied in human lymphocytes in vitro after treatment with singlet oxygen. When produced outside the cells, singlet oxygen can increase the duration of the cellular cycle as measured by an enhancement of the differences between the proliferation rate indexes of the control and the treated cells. A dose-dependent increase in the SCE rate per chromosome was also detected after contact between the singlet oxygen and lymphocytes.