RESUMO
BACKGROUND: Nitroglycerin is a vasodilator that has been reported to improve cutaneous flap and graft survival. It has not been tested in controlled studies. OBJECTIVE: We designed our study to test the effectiveness of a single postoperative application of nitroglycerin on flap and graft survival. METHODS: Eighty-eight surgical repairs received topical nitroglycerin and 85 received control ointment (polysporin). Treatment sites were evaluated on postoperative day 7 and assigned a percentage of surface area survival. RESULTS: There was no significant difference in the complication rate of flaps and grafts treated with nitroglycerin (12.5%) compared with those treated with control ointment (8.4%) (P = .244). Subset analysis of flaps as a group and grafts as a group were not meaningful because the complication rates were so low. CONCLUSION: There is no survival increase of flaps and grafts treated with a single application of nitroglycerin ointment.
Assuntos
Sobrevivência de Enxerto/efeitos dos fármacos , Nitroglicerina/administração & dosagem , Transplante de Pele , Retalhos Cirúrgicos , Vasodilatadores/administração & dosagem , Cicatrização/efeitos dos fármacos , Administração Cutânea , Intervalo Livre de Doença , Método Duplo-Cego , Humanos , Cirurgia de Mohs , Pomadas , Cuidados Pós-Operatórios , Neoplasias Cutâneas/cirurgia , Resultado do TratamentoRESUMO
Proteins of the membrane skeleton of Euglena gracilis were extensively phosphorylated in vivo and in vitro after incubation with [32P]-orthophosphate or gamma-[32P] ATP. Endogenous protein threonine/serine activity phosphorylated the major membrane skeletal proteins (articulins) and the putative integral membrane protein (IP39) anchor for articulins. The latter was also the major target for endogenous protein tyrosine kinase activity. A cytoplasmic domain of IP39 was specifically phosphorylated, and removal of this domain with papain eliminated the radiolabeled phosphoamino acids and eliminated or radically shifted the PI of the multiple isoforms of IP39. In gel kinase assays IP39 autophosphorylated and a 25 kDa protein which does not autophosphorylate was identified as a threonine/serine (casein) kinase. Plasma membranes from the membrane skeletal protein complex contained threonine/serine (casein) kinase activity, and cross-linking experiments suggested that IP39 was the likely source for this membrane activity. pH optima, cation requirements and heparin sensitivity of the detergent solubilized membrane activity were determined. Together these results suggest that protein kinases may be important modulators of protein assembly and function of the membrane skeleton of these protistan cells.
Assuntos
Proteínas do Citoesqueleto/metabolismo , Euglena gracilis/enzimologia , Proteínas de Membrana/metabolismo , Proteínas Serina-Treonina Quinases/metabolismo , Proteínas Tirosina Quinases/metabolismo , Proteínas de Protozoários/metabolismo , Trifosfato de Adenosina/metabolismo , Animais , Caseína Quinases , Cátions Bivalentes/farmacologia , Membrana Celular/enzimologia , Membrana Celular/metabolismo , Reagentes de Ligações Cruzadas , Euglena gracilis/metabolismo , Heparina/farmacologia , Concentração de Íons de Hidrogênio , Ponto Isoelétrico , Proteínas de Membrana/química , Papaína , Mapeamento de Peptídeos , Fosforilação , Proteínas Quinases/metabolismo , Proteínas de Protozoários/químicaRESUMO
BACKGROUND AND DESIGN: A recent animal study indicated that epinephrine in local anesthesia adversely affects the survival of full-thickness skin grafts. Because animal models do not always correlate to humans, we performed a prospective observational study to elucidate the clinical outcome of using epinephrine in local anesthesia of the donor site. Seventy-two patients had cutaneous tumors excised by the Mohs micrographic technique. The resultant surgical defects were repaired using full-thickness skin grafts. Patients were randomly divided into two groups based on the local anesthetic used at the donor site: (1) 1% lidocaine (Xylocaine) (n = 33) or (2) 1% lidocaine with 1:100,000 epinephrine (n = 39). RESULTS: Assessment of the skin grafts at 1 week revealed a significantly increased risk of developing graft complications in the lidocaine with epinephrine group compared with the plain lidocaine group. The overall cosmetic outcome of the grafted site at 6 weeks revealed no significant difference between the two groups. CONCLUSIONS: Because there was only a minimal clinical effect of epinephrine on graft survival observed at 1 week and there was no effect on the 6-week cosmetic outcome, we do not recommend harvesting all full-thickness skin grafts with plain lidocaine. In certain clinical circumstances with compromised vascular supply or poor oxygenation, the use of plain lidocaine may be advantageous.
Assuntos
Anestesia Local , Procedimentos Cirúrgicos Dermatológicos , Epinefrina/farmacologia , Lidocaína/administração & dosagem , Transplante de Pele/métodos , Idoso , Epinefrina/efeitos adversos , Estética , Neoplasias Faciais/cirurgia , Feminino , Sobrevivência de Enxerto/efeitos dos fármacos , Humanos , Masculino , Cirurgia de Mohs , Necrose , Estudos Prospectivos , Fatores de Risco , Pele/efeitos dos fármacos , Pele/patologia , Neoplasias Cutâneas/cirurgia , Transplante de Pele/efeitos adversos , Transplante de Pele/patologia , Resultado do TratamentoRESUMO
Several "progeroid" syndromes have now been identified. The De Barsy syndrome is an autosomal recessive syndrome of dwarfism, mental deficiency, an "aged" appearance at birth, abnormal elastic fibers on skin biopsy, and lax skin, large helices, eye abnormalities, lax joints, hypotonia, and athetoid posturing. We report one case and review 11 cases from the literature. To understand the abnormal appearance of the elastic fibers on biopsy, we performed elastin gene expression studies on fibroblasts cultured from our patient's skin. Molecular hybridization studies revealed reduced elastin mRNA steady-state levels as compared with age matched control individuals. Assuming normal rates of mRNA translation, reduced elastin synthesis would occur. Diminished dermal elastin content could explain the altered cutaneous elasticity, decreased elastic fibers in the skin, and many clinical manifestations of individuals with this condition.
Assuntos
Elastina/genética , Progéria/genética , Pré-Escolar , Diagnóstico Diferencial , Feminino , Expressão Gênica , Humanos , Fenótipo , Progéria/diagnóstico , Progéria/fisiopatologia , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Pele/metabolismo , Pele/patologia , SíndromeRESUMO
The author presents the results of a study of 200 patients with surgical defects of the nose following excision of skin malignancies. The location, size, depth, and quality of the adjacent skin, the reconstruction choice, and the cosmetic result were recorded. Healing by second intention was most useful for wounds in concave areas. Full-thickness skin grafts were used for defects too large for local flaps, or for defects on the nasal tip or alar surface. Local flaps were the most useful choice for nasal reconstruction. Transposition flaps, in particular, were most useful for each cosmetic sub unit of the nose.
Assuntos
Nariz/cirurgia , Retalhos Cirúrgicos/métodos , HumanosRESUMO
To delineate cis-acting regulatory elements of the human elastin gene, several elastin promoter region/chloramphenicol acetyltransferase reporter gene constructs were developed. The spectrum of inserts, spanning from -2260 to +2, was shown to contain several SP-1 and AP2 binding sites, as well as putative glucocorticoid, cAMP, and 12-O-tetradecanoylphorbol-13-acetate responsive elements. Assay of promoter activity in transient transfections of rat aortic smooth muscle cells, human skin fibroblasts, HT-1080 human fibrosarcoma cells, HeLa cells, or mouse NIH-3T3 cells allowed delineation of several functional subregions within 2.26 kilobases of the 5'-flanking DNA. The results suggest that the basic promoter element resides within the region -128 to -1, and the 5'-flanking DNA contains several functional regulatory subregions. Also, the regulatory function of three putative SP-1 binding sites was demonstrated by transfections with a plasmid devoid of such sequences. These findings attest to the complexity of transcriptional regulation of the elastin gene.
Assuntos
Elastina/genética , Regiões Promotoras Genéticas/genética , Sequências Reguladoras de Ácido Nucleico , Animais , Aorta , Sequência de Bases , Sítios de Ligação , Deleção Cromossômica , Clonagem Molecular , AMP Cíclico/farmacologia , Proteínas de Ligação a DNA/metabolismo , Fibroblastos/metabolismo , Fibrossarcoma/metabolismo , Glucocorticoides/farmacologia , Células HeLa , Humanos , Dados de Sequência Molecular , Músculo Liso Vascular/metabolismo , Plasmídeos , Reação em Cadeia da Polimerase , Ratos , Fator de Transcrição Sp1 , Acetato de Tetradecanoilforbol/farmacologia , Fatores de Transcrição/metabolismo , Transfecção , Células Tumorais CultivadasRESUMO
Nidogen, a multifunctional glycoprotein, is an integral part of all basement membranes. In this study, human nidogen cDNAs were isolated and characterized from human placental and skin fibroblast cDNA libraries by hybridization with a mouse nidogen cDNA probe. Six overlapping clones covering 4.9 kb were characterized. The composite cDNA contained a 3,741-nucleotide open reading frame which coded for a 1,247-amino-acid peptide that included a hydrophobic signal sequence. The deduced amino acid sequence contains seven epidermal growth factor-like cysteine-rich repeats, one possible tyrosine O-sulfation site, and a possible N-glycosylation site. The tripeptide sequence -Arg-Gly-Asp- (RGD), a potential cell attachment site, was also present. Human and mouse nidogen sequences were 84% homologous at the nucleotide level and 85% homologous at the deduced amino acid level. Southern blotting of human leukocyte DNA from 23 individuals indicated that nidogen probably is a single-copy gene and shows multiple restriction fragment length polymorphisms when cleaved with Eco RI, Pvu II, Taq I, and Msp I. In particular, digestions with Pvu II revealed polymorphism in four discrete DNA fragments, which could be discriminated by hybridizations with nidogen subclones. One of the polymorphisms revealed an allelic frequency of 0.52/0.48. Thus, human nidogen gene displays RFLPs which provide analytical tools to establish genetic linkage between the nidogen gene and a clinical phenotype.