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1.
Neuroscience ; 412: 207-215, 2019 08 01.
Article in English | MEDLINE | ID: mdl-31220545

ABSTRACT

High voltage-activated (HVA) Ca2+ (CaV) channels are oligomeric complexes formed by an ion-conducting main subunit (Cavα1) and at least two auxiliary subunits (Cavß and CaVα2δ). It has been reported that the expression of CaVα2δ1 increases in the dorsal root ganglia (DRGs) of animals with mechanical allodynia, and that the transcription factor Sp1 regulates the expression of the auxiliary subunit. Hence, the main aim of this work was to investigate the role of Sp1 as a molecular determinant of the exacerbated expression of CaVα2δ-1 in the nerve ligation-induced model of mechanical allodynia. Our results show that ligation of L5/L6 spinal nerves (SNL) produced allodynia and increased the expression of Sp1 and CaVα2δ-1 in the DRGs. Interestingly, intrathecal administration of the Sp1 inhibitor mithramycin A (Mth) prevented allodynia and decreased the expression of Sp1 and CaVα2δ-1. Likewise, electrophysiological recordings showed that incubation with Mth decreased Ca2+ current density in the DRG neurons, acting mostly on HVA channels. These results suggest that L5/L6 SNL produces mechanical allodynia and increases the expression of the transcription factor Sp1 and the subunit CaVα2δ-1 in the DRGs, while Mth decreases mechanical allodynia and Ca2+ currents through HVA channels in sensory neurons by reducing the functional expression of the CaVα2δ-1 subunit.


Subject(s)
Calcium Channels/metabolism , Ganglia, Spinal/metabolism , Neuralgia/metabolism , Sensory Receptor Cells/metabolism , Sp1 Transcription Factor/metabolism , Animals , Female , Ganglia, Spinal/drug effects , Neuralgia/etiology , Peripheral Nerve Injuries/complications , Peripheral Nerve Injuries/metabolism , Plicamycin/analogs & derivatives , Plicamycin/pharmacology , Rats, Wistar , Sensory Receptor Cells/drug effects , Sp1 Transcription Factor/antagonists & inhibitors
2.
Lasers Med Sci ; 32(2): 305-315, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27924419

ABSTRACT

The use of low-level laser for lung inflammation treatment has been evidenced in animal studies as well as clinical trials. The laser action mechanism seems to involve downregulation of neutrophil chemoattractants and transcription factors. Innate immune responses against microorganisms may be mediated by toll-like receptors (TLR). Intestinal ischemia and reperfusion (i-I/R) lead to bacterial product translocation, such as endotoxin, which consequently activates TLRs leading to intestinal and lung inflammation after gut trauma. Thus, the target of this study was to investigate the role of TLR activation in the laser (660 nm, 30 mW, 67.5 J/cm2, 0.375 mW/cm2, 5.4 J, 180 s, and spot size with 0.08 cm2) effect applied in contact with the skin on axillary lymph node in lung inflammation induced by i-I/R through a signaling adaptor protein known as myeloid differentiation factor 88 (MyD88). It is a quantitative, experimental, and laboratory research using the C57Bl/6 and MyD88-/- mice (n = 6 mice for experimental group). Statistical differences were evaluated by ANOVA and the Tukey-Kramer multiple comparisons test to determine differences among groups. In order to understand how the absence of MyD88 can interfere in the laser effect on lung inflammation, MyD88-/- mice were treated or not with laser and subjected to occlusion of the superior mesenteric artery (45 min) followed by intestinal reperfusion (4 h). In summary, the laser decreased the MPO activity and the lung vascular permeability, thickened the alveolar septa, reduced both the edema and the alveolar hemorrhage, as well as significantly decreased neutrophils infiltration in MyD88-deficient mice as well in wild-type mice. It noted a downregulation in chemokine IL-8 production as well as a cytokine IL-10 upregulation in these animals. The results also evidenced that in absence of IL-10, the laser effect is reversed. Based on these results, we suggest that the beneficial effect of laser in acute lung injury after i-I/R is dependent on the secretion of IL-10 and independent of the TLR/MyD88 signaling.


Subject(s)
Acute Lung Injury/radiotherapy , Interleukin-10/metabolism , Intestines/blood supply , Low-Level Light Therapy/methods , Myeloid Differentiation Factor 88/metabolism , Reperfusion Injury/pathology , Signal Transduction , Toll-Like Receptors/metabolism , Acute Lung Injury/complications , Acute Lung Injury/genetics , Animals , Gene Expression Regulation/drug effects , Inflammation/metabolism , Intercellular Adhesion Molecule-1/metabolism , Interleukin-10/genetics , Interleukin-8/genetics , Interleukin-8/metabolism , Intestines/pathology , Lung/blood supply , Lung/metabolism , Lung/pathology , Mice, Inbred C57BL , Microvessels/drug effects , Microvessels/pathology , Peroxidase/metabolism , Plicamycin/pharmacology , RNA, Messenger/genetics , RNA, Messenger/metabolism , Reperfusion Injury/complications , Reperfusion Injury/metabolism , Signal Transduction/drug effects
3.
Mar Drugs ; 12(12): 5839-55, 2014 Dec 04.
Article in English | MEDLINE | ID: mdl-25486109

ABSTRACT

The present study highlights the biological effects of chromomycin A2 toward metastatic melanoma cells in culture. Besides chromomycin A2, chromomycin A3 and demethylchromomycin A2 were also identified from the extract derived from Streptomyces sp., recovered from Paracuru Beach, located in the northeast region of Brazil. The cytotoxic activity of chromomycin A2 was evaluated across a panel of human tumor cell lines, which found IC50 values in the nM-range for exposures of 48 and 72 h. MALME-3M, a metastatic melanoma cell line, showed the highest sensitivity to chromomycin A2 after 48h incubation, and was chosen as a model to investigate this potent cytotoxic effect. Treatment with chromomycin A2 at 30 nM reduced cell proliferation, but had no significant effect upon cell viability. Additionally, chromomycin A2 induced accumulation of cells in G0/G1 phase of the cell cycle, with consequent reduction of S and G2/M and unbalanced expression of cyclins. Chromomycin A2 treated cells depicted several cellular fragments resembling autophagosomes and increased expression of proteins LC3-A and LC3-B. Moreover, exposure to chromomycin A2 also induced the appearance of acidic vacuolar organelles in treated cells. These features combined are suggestive of the induction of autophagy promoted by chromomycin A2, a feature not previously described for chromomycins.


Subject(s)
Autophagy/drug effects , Melanoma/drug therapy , Plicamycin/analogs & derivatives , Brazil , Cell Cycle/drug effects , Cell Line, Tumor , Cell Proliferation/drug effects , Cell Survival/drug effects , Chromomycin A3/metabolism , Chromomycins/pharmacology , HCT116 Cells , HL-60 Cells , Humans , Melanoma/metabolism , Microtubule-Associated Proteins/metabolism , Plicamycin/pharmacology , Streptomyces/chemistry
4.
J Interferon Cytokine Res ; 32(10): 495-504, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22873641

ABSTRACT

Double-stranded RNA dependent protein kinase (PKR) is a host defense enzyme whose expression is up-regulated in response to interferons (IFNs) and during viral infections. Increased levels of PKR can result in its activation, which, in turn, inhibits global cellular protein synthesis. Despite growing evidence suggesting the involvement of PKR in bacterial infections, little is known about its expression, regulation and cellular role in nonviral infections. The aim of this work was to determine the expression and regulation of PKR in response to stimulation of human THP-1 monocytes with bacterial agonists of TLR2/4. Treatment of cells with Pam3CSK4 or lipopolyssacharide (LPS) resulted in an increase in PKR mRNA and protein levels. Robust PKR expression at later times correlated with a decrease in global protein synthesis. PKR was also required to regulate the inhibition of protein synthesis triggered by LPS in mouse splenocytes. Surprisingly, no increase of IFN-ß or IFN-α mRNA levels was detected after treatment of THP-1 cells with toll-like receptor (TLR) agonists. In accordance with this, the supernatants from LPS or Pam3CSK4-treated cells lacked the ability to activate the PKR and ISG56 promoters in gene reporter assays carried out in HEK293T cells. The expression of PKR induced by TLRs agonists was dramatically impaired when cells were treated in the presence of tosyl-phenylalanyl chloromethylketone or Mithramycin, suggesting that NF-κB and Sp1 transcription factors, but not those activated by IFNs, regulate the expression of PKR in human monocytes.


Subject(s)
Bacterial Infections/immunology , Monocytes/immunology , NF-kappa B/metabolism , Sp1 Transcription Factor/metabolism , Toll-Like Receptor 2/agonists , Toll-Like Receptor 4/agonists , eIF-2 Kinase/metabolism , Adaptor Proteins, Signal Transducing , Animals , Gene Expression Regulation, Bacterial/drug effects , Gene Expression Regulation, Bacterial/genetics , HEK293 Cells , Humans , Interferons/immunology , Lipopeptides/pharmacology , Lipopolysaccharides/pharmacology , Mice , Mice, Knockout , Monocytes/drug effects , Monocytes/microbiology , NF-kappa B/genetics , Plicamycin/pharmacology , Protein Synthesis Inhibitors/pharmacology , RNA-Binding Proteins , Sp1 Transcription Factor/genetics , Tosylphenylalanyl Chloromethyl Ketone/pharmacology , Transcription Factors/genetics , eIF-2 Kinase/genetics
5.
J Nat Prod ; 65(8): 1091-5, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12193009

ABSTRACT

Tat is a small HIV protein essential for both viral replication and the progression of HIV disease. In our efforts to discover Tat inhibitors from natural product screening of microbial fermentation extracts, we discovered durhamycin A (1) as a potent inhibitor (IC(50) = 4.8 nM) of Tat transactivation. Detailed NMR and MS/MS studies were utilized to elucidate the structure of 1 as a new member of the aureolic acid family of antibiotics. It consists of tetrasaccharide and disaccharide moieties attached to the aglycone, which is hitherto unknown in the aureolic acid family. Three other novel analogues, durhamycin B (2), compound (3), and the aglycone (4), were also discovered or chemically prepared that were less potent than durhamycin A.


Subject(s)
Anti-HIV Agents/pharmacology , Gene Products, tat/antagonists & inhibitors , Gene Products, tat/physiology , HIV-1/physiology , Plicamycin/analogs & derivatives , Costa Rica , Drug Design , Gene Expression Regulation, Viral , Gene Products, tat/metabolism , Hydrolysis , Inhibitory Concentration 50 , Magnetic Resonance Spectroscopy , Mass Spectrometry , Molecular Structure , Plicamycin/pharmacology , Protein Binding/drug effects , Structure-Activity Relationship , Substrate Specificity , tat Gene Products, Human Immunodeficiency Virus
6.
Chromosoma ; 109(3): 197-200, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10929198

ABSTRACT

Chromosomes of a species of Eigenmannia presenting a X1X1X2X2:X1X2Y sex chromosome system, resulting from a Y-autosome Robertsonian translocation, were analyzed using the C-banding technique, chromomycin A3 (CMA3) and mithramycin (MM) staining and in situ digestion by the restriction endonuclease AluI. A comparison of the metacentric Y chromosome of males with the corresponding acrocentrics in females indicated that a C-band-positive, CMA3/MM-fluorescent and AluI digestion-resistant region had been lost during the process of translocation, resulting in a diminution of heterochromatin in the males. It is hypothesized that the presence of a smaller amount of G + C-rich heterochromatin in the sex chromosomes of the heteromorphic sex when compared with the homomorphic sex may be associated with the sex determination mechanism in this species and may be a more widely occurring phenomenon in fish with differentiated sex chromosomes than was initially thought.


Subject(s)
Biological Evolution , Electric Fish/genetics , Sex Chromosomes/genetics , Animals , Chromomycin A3/chemistry , Female , Heterochromatin , Karyotyping , Male , Plicamycin/chemistry , Restriction Mapping , Sex Differentiation , Silver Staining/methods , Translocation, Genetic
7.
Cytogenet Cell Genet ; 78(1): 36-43, 1997.
Article in English | MEDLINE | ID: mdl-9345903

ABSTRACT

The genome sizes of the Venezuelan spiny-rats Proechimys guairae guairae (2n = 48) and P. trinitatis (2n = 62) were evaluated and proved to be 12.5 +/- 0.5 pg and 12.6 +/- 0.3 pg respectively, the highest so far recorded among mammals; also the C-heterochromatin (32.7%, Coefficient of Variation [CV] 3.8 and 35.8%, CV 4.4) and GC (44.2%, CV 2.7 and 43.6%, CV 2.9) contents are very high. Highly repetitive (rep) DNAs were isolated from restriction enzyme digested genomic DNAs of both species. The intra- and inter-specific chromosomal allocations of these rep DNAs were analyzed by direct and cross-hybridizations. Results show that the two genomes harbour several rep DNA families which show both species-specificity and interspecific relatedness in their in situ hybridization patterns. The rep DNA families show an equilocal distribution at both the pericentromeric areas of all chromosomes and in the whole arms of two pairs of the uniarmed group, suggesting co-evolution of the rep DNAs. P. g. guairae BamHI digested DNA, when cloned and sequenced, proved to consist of a long "composite" unit (1,239 bp) containing two copies of each of 75-bp and 110-bp internal subrepeats. Karyotype restructuring between P. g. guairae and P. trinitatis, mainly due to Robertsonian changes, was accompanied by slight intra- and intergenomic movements of the putative satellite DNA families within stable genome sizes and C-heterochromatin contents. We discuss the findings obtained in Proechimys in the light of those regarding the kangaroo rat, the pocket gopher and the house mouse; they support the idea that karyotype restructuring could be the expression of molecular driven events of rep DNA amplification and homogenisation through non-homologous chromosomes.


Subject(s)
Heterochromatin/genetics , Repetitive Sequences, Nucleic Acid , Rodentia/genetics , Animals , Base Sequence , Bisbenzimidazole , Chromosome Banding , DNA/analysis , Deoxyribonuclease BamHI , Deoxyribonucleases, Type II Site-Specific , Dipodomys , Evolution, Molecular , Female , Fluorescent Dyes , Genome , In Situ Hybridization, Fluorescence , Intercalating Agents , Karyotyping , Male , Mice , Mice, Inbred C3H , Molecular Sequence Data , Plicamycin/analogs & derivatives , Restriction Mapping , Species Specificity
9.
West Indian med. j ; West Indian med. j;40(Suppl. 2): 122-3, July 1991.
Article in English | MedCarib | ID: med-5177

ABSTRACT

A review of the condition originally described by Sir James Paget in 1877 as osteitis deformans and suggesting an infectious origin, together with its cardinal symptoms is undertaken in the light of contemporary knowledge and with today's technology. An analysis of its presenting symptoms, its cardinal signs and differential diagnosis is considered and a look at electron microscopical evidence demonstrates that its original description may yet be proven to be aetiologically accurate. A review of current treatment methods including the use of salmon calcitonin, mithramycin, and etidronate disodium (diphosphonate) is undertaken. The advantages are discussed and an approach to treatment identifies that both calcitonin and diphosphonate therapies in appropriate cycles do achieve the desired result in the majority of cases. A case report of a successfully treated patient with an extensively diseased tibia is demonstrated and discussed (AU)


Subject(s)
Humans , Paget's Disease, Mammary , Osteitis Deformans , Osteitis Deformans , Calcitonin , Plicamycin , Etidronic Acid
10.
Rev. cuba. oncol ; 3(1): 67-71, ene.-abr. 1987. ilus, tab
Article in Spanish | LILACS | ID: lil-53189

ABSTRACT

Se obtuvieron algunos derivados del aureol y se evaluó la capacidad de éstos de competir con el estradiol por enlazarse con el receptor de estradiol de útero de rata. Se comprobó que al igual que el aureol, todos los compuestos desplazan al estradiol; el dibromo aureol es el que presenta mayor afinidad por el receptor y se compara su afinidad con la del antiestrógeno tamoxifén


Subject(s)
Rats , Animals , Estradiol/therapeutic use , Plicamycin/therapeutic use , Uterine Neoplasms
15.
J Nutr ; 59(1): 155-70, May 1956.
Article in English | MedCarib | ID: med-15732

ABSTRACT

A study was made to examine the influence of vitamin B12 and aureomycin upon the growth in protein-deficient children. The results of this study present evidence for a slight positive effect of aureomycin upon the rate of weight increase, but no effect upon the rate of height increase. The result show that vitamin B12 has no positive effect upon weight or height increments. The nutritional status was observed to be low. Among the observations made were clinical examinations, growth measurements, biochemical measurements and a direct dietary survey. There is no evidence to suggest that either aureomycin or vitamin B12 would be of practical value in alleviating the malnutrition found in such areas as the Caribbean. (summary)


Subject(s)
Humans , Child , Male , Female , Vitamin B 12/therapeutic use , Plicamycin/therapeutic use , Protein Deficiency/therapy , Growth , Nutritional Status , Body Height , Body Weight , Jamaica
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