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1.
J. venom. anim. toxins incl. trop. dis ; 18(3): 277-286, 2012. ilus, graf
Article in English | LILACS | ID: lil-649475

ABSTRACT

Envenomation by Loxosceles bites is characterized by dermonecrotic and/or systemic features that lead to several clinical signs and symptoms called loxoscelism. Dermonecrotic lesions are preceded by thrombosis of the dermal plexus. Recent studies show that atheromatous plaque is prone to thrombosis due to endothelial cell apoptosis. To the best of our knowledge, there are no reports of microscopic dermal lesion and endothelial cell apoptosis induced by Loxosceles similis venom in the literature. Thus, the aim of the present study is to describe histological lesions induced by L. similis venom in rabbit skin and to elucidate whether apoptosis of endothelial cells is involved in the pathogenesis of loxoscelism. Forty male rabbits were split into two groups: the control group (intradermally injected with 50 µL of PBS) and the experimental group (intradermally injected with 0.5 µg of L. similis crude venom diluted in 50 µL of PBS). After 2, 4, 6 and 8 hours of injection, skin fragments were collected and processed for paraffin or methacrylate embedding. Sections of 5 µm thick were stained by HE, PAS or submitted to TUNEL reaction. Microscopically, severe edema, diffuse heterophilic inflammatory infiltrate, perivascular heterophilic infiltrate, thrombosis, fibrinoid necrosis of arteriolar wall and cutaneous muscle necrosis were observed. Two hours after venom injection, endothelial cells with apoptosis morphology were evidenced in the dermal plexus. Apoptosis was confirmed by TUNEL reaction. It seems that endothelial cell apoptosis and its consequent desquamation is an important factor that induces thrombosis and culminates in dermonecrosis, which is characteristic of cutaneous loxoscelism.


Subject(s)
Animals , Male , Rabbits , Poisoning/pathology , Skin/pathology , Spider Venoms , Rabbits/injuries
2.
J. venom. anim. toxins incl. trop. dis ; 14(2): 274-293, 2008. ilus, tab
Article in English | LILACS | ID: lil-484564

ABSTRACT

Insect-pests are global problems that cause severe damage to crop plants, and their control is commonly based on chemical insecticides. However, negative effects of pesticides on the environment and human health emphasize the necessity to develop alternative methods for insect-pest control. In the present study, a gene coding for the insecticidal peptide TX4(6-1) of the Brazilian armed spider (Phoneutria nigriventer) was cloned in fusion with maltose binding protein (MBP) and expressed in Escherichia coli. The affinity purified protein MBP-GlyTX4 was cleaved with the Xa factor and used for a bioassay against Spodoptera frugiperda and rabbit immunization. Five micrograms GlyTX4 protein injected into the hemocoel of larvae and abdominal cavity of adults produced trembling and uncoordinated movements immediately after injection and all adult insects died after 12h. After two days, larvae became paralyzed and the epidermal color changed to dark brown. Furthermore, the development stage was prolonged for two weeks. Alternatively, slices of maize leaves were imbibed with 15 micrograms of the recombinant protein cleaved with the Xa factor and used as diet for larvae. In this experiment, all larvae died in about 30 minutes. Polyclonal antibodies anti-MBP-GlyTX4 were effective for recognizing MBP and GlyTX4 in whole cell extract from E. coli expressing the recombinant protein.


Subject(s)
Animals , Cloning, Molecular/methods , Escherichia coli , Insect Control , Pest Control, Biological , Spodoptera
3.
Braz. j. med. biol. res ; 40(4): 583-590, Apr. 2007. graf
Article in English | LILACS | ID: lil-445658

ABSTRACT

The relationship between preeclampsia and the renin-angiotensin system (RAS) is poorly understood. Angiotensin I-converting enzyme (ACE) is a key RAS component and plays an important role in blood pressure homeostasis by generating angiotensin II (Ang II) and inactivating the vasodilator angiotensin-(1-7) (Ang-(1-7)). ACE (I/D) polymorphism is characterized by the insertion (I) or deletion (D) of a 287-bp fragment, leading to changes in ACE activity. In the present study, ACE (I/D) polymorphism was correlated with plasma Ang-(1-7) levels and several RAS components in both preeclamptic (N = 20) and normotensive pregnant women (N = 20). The percentage of the ACE DD genotype (60 percent) in the preeclamptic group was higher than that for the control group (35 percent); however, this percentage was not statistically significant (Fisher exact test = 2.86, d.f. = 2, P = 0.260). The highest plasma ACE activity was observed in the ACE DD preeclamptic women (58.1 ± 5.06 vs 27.6 ± 3.25 nmol Hip-His Leu-1 min-1 mL-1 in DD control patients; P = 0.0005). Plasma renin activity was markedly reduced in preeclampsia (0.81 ± 0.2 vs 3.43 ± 0.8 ng Ang I mL plasma-1 h-1 in DD normotensive patients; P = 0.0012). A reduced plasma level of Ang-(1-7) was also observed in preeclamptic women (15.6 ± 1.3 vs 22.7 ± 2.5 pg/mL in the DD control group; P = 0.0146). In contrast, plasma Ang II levels were unchanged in preeclamptic patients. The selective changes in the RAS described in the present study suggest that the ACE DD genotype may be used as a marker for susceptibility to preeclampsia.


Subject(s)
Adult , Female , Humans , Pregnancy , Angiotensin I/blood , Gene Deletion , Peptide Fragments/blood , Peptidyl-Dipeptidase A/genetics , Polymorphism, Genetic/genetics , Pre-Eclampsia/blood , Renin/blood , Angiotensin II/blood , Case-Control Studies , Renin-Angiotensin System
4.
Genet. mol. res. (Online) ; 6(4): 1026-1034, 2007. ilus, tab
Article in English | LILACS | ID: lil-520047

ABSTRACT

We described five novel microsatellite loci for the piracema fish species Prochilodus lineatus (Characiformes), endemic to South America and of extreme importance to both commercial and artisanal fisheries across its occurrence area. A primary, unenriched genomic library was constructed and radioactively screened for repetitive motifs. Positive clones were automatically sequenced and based on the design of new primers, polymerase chain reaction assays were carried out to determine optimum reaction and electrophoretic conditions for each characterized locus. We evaluated its usefulness in population genetic studies by determining Hardy-Weinberg equilibrium, FIS and a jackknife estimate of the number of alleles for a sample of fish caught below the Funil Hydroelectric Power Plant dam (N = 95), Grande River, Brazil. The number of alleles varied from 3 to 21 and expected heterozygosities ranged from 0.58 to 0.91. Two of five loci were in Hardy-Weinberg equilibrium. Jackknife estimates of the number of alleles were higher than the observed number of alleles for three loci and could provide a measure of sampling bias. These markers should provide important tools for the determination of genetic structure, stock delimitation and reservoir fish management in the Grande River as well as to improve hatchery practices for environmental mitigation measures and to help sustain fisheries in the river.


Subject(s)
Animals , Genetics, Population , Genomic Library , Microsatellite Repeats , Fishes/genetics , Alleles , Base Sequence , Brazil , DNA , Heterozygote , Plasmids , DNA Primers/genetics
5.
Braz. j. med. biol. res ; 21(5): 961-9, 1988. ilus
Article in English | LILACS | ID: lil-63591

ABSTRACT

1. Adult Schistosoma mansoni show a proclivity to release fragments of the tegumental surface membrane when they are incubated in various media, or after they are exposed to posirively chaged microspheres. Scanning electron microscopy was used to examine the extent and nature of the pertubations induced by the two treatment used to prepare tegumental membranes. Incubation of the parasites in a phosphate - buffered medium resulted in extensive blebbing and release of vesicles from the tegument. 3. Attachment of positively charged microspheres followed by their release yelded tegument membrane fragments of a different morphology. 4. The nature and implications of these pertubations to membrane processes occuring at the tegument of schistosomes are discussed


Subject(s)
Animals , Male , Female , Schistosoma mansoni/ultrastructure , Cell Membrane/ultrastructure , Culture Media , Microspheres
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