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1.
Rev Gastroenterol Mex ; 78(4): 225-30, 2013.
Article in Spanish | MEDLINE | ID: mdl-24290317

ABSTRACT

BACKGROUND: Peroral endoscopic myotomy has recently been developed and performed on patients with good results. AIMS: To evaluate the technical feasibility of peroral endoscopic full-thickness and partial thickness myotomy in a porcine model. MATERIAL AND METHODS: Eighteen criollo pigs were randomly assigned to 2 groups: group A (partial-thickness myotomy) and group B (full-thickness myotomy). The mucosal defect proximal to the myotomy site was left open. On the seventh postoperative day the pig was euthanized and follow-up surgical exploration was performed. The duration of each procedure, postoperative progression of the animal, complications, and anatomopathologic findings were registered. RESULTS: The procedure was viable in all the pigs. The mean surgery duration was 81±35.3min (group A 51.11±11.12, group B 111±22.61; P<.05). The main complication during myotomy was subcutaneous emphysema (16%). The histopathologic study of the group A surgical specimens reported complete circular myotomy in all cases, and complete circular and longitudinal myotomy was reported in 100% of the group B sample. CONCLUSIONS: The endoscopic myotomy technique is feasible. Endoscopic partial-thickness myotomy was associated with shorter surgery duration and better results during the intraoperative period and the 7-day follow-up.


Subject(s)
Endoscopy, Gastrointestinal/methods , Esophagus/surgery , Mouth/surgery , Anesthesia , Animals , Endoscopy, Gastrointestinal/adverse effects , Esophageal Achalasia/surgery , Esophageal Sphincter, Lower/surgery , Female , Muscles/surgery , Natural Orifice Endoscopic Surgery , Postoperative Hemorrhage , Swine
2.
Ann Rheum Dis ; 60(8): 791-5, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11454644

ABSTRACT

OBJECTIVE: To study the association between rheumatoid arthritis (RA) and HLA and tumour necrosis factor (TNF) polymorphism in Peruvian mestizo patients in comparison with ethnically similar controls. METHODS: Seventy nine patients with RA and 65 ethnically matched healthy controls were genotyped for HLA-DRB1, HLA-DQA1, HLA-DQB1, and TNFalpha and TNFbeta alleles using PCR amplification. Clinical severity was assessed as mild, moderate, or severe in 35 of the patients. RESULTS: TNFalpha6 showed the strongest association with disease susceptibility. The TNFalpha6 allele was more common in patients than in controls (p<0.0076) and the proportion of patients with at least one copy of this allele was greater (p<0.015, relative risk 2.35). Among the HLA-DRB1* alleles with the shared epitope sequence, only the DRB1*1402 allele was significantly increased in patients compared with controls (p<0.0311), as was the proportion of patients with at least one copy of this allele (p<0.0232, relative risk 2.74). In contrast, the overall frequency of alleles with the shared epitope was not different in patients and controls. The haplotype HLA-DRB1*1402-DQB1*0301-DQA1*0401 was significantly more common in patients. TNFalpha6 was more common in patients whether or not they had this haplotype. None of the 11 patients lacking the TNFalpha6 allele had severe disease. CONCLUSIONS: This study shows for the first time that TNF gene polymorphism is associated with susceptibility to RA in a non-white population. TNFalpha6 and HLA-DRB1*1402 independently conferred significantly increased risk in Peruvian mestizo patients.


Subject(s)
Arthritis, Rheumatoid/genetics , HLA-DQ Antigens/genetics , HLA-DR Antigens/genetics , Microsatellite Repeats/genetics , Tumor Necrosis Factor-alpha/genetics , Alleles , Case-Control Studies , Epitopes/genetics , Gene Frequency , Genetic Predisposition to Disease , Genotype , HLA-DQ alpha-Chains , HLA-DQ beta-Chains , HLA-DRB1 Chains , Haplotypes/genetics , Humans , Peru , Polymerase Chain Reaction , Polymorphism, Genetic
3.
Brain Res Mol Brain Res ; 60(1): 133-9, 1998 Sep 18.
Article in English | MEDLINE | ID: mdl-9748541

ABSTRACT

Opioids have been implicated in sexual differentiation of the brain and in the regulation of reproductive behavior and endocrinology of mammals. Previous studies have indicated that estrogen administration in adults regulates preproenkephalin MRNA levels in several hypothalamic brain nuclei. We have determined preproenkephalin mRNA levels in estrogen-treated juvenile male and female rats to investigate the developmental pattern of estrogenic regulation of enkephalinergic neurons in the medial preoptic area. Rats were treated with estradiol benzoate (20 microgram/kg/day) or oil from day 21 to 23. Sections of the medial preoptic area (mPOA) were studied by in situ hybridization histochemistry at the single cell level and quantified with the assistance of an image analysis system. Our data indicate that males contain higher levels of preproenkephalin mRNA per neuron than females. In addition, our results indicate that estrogen causes an upward shift in the amount of mRNA expressed per cell, females demonstrating a greater response to estrogen than males. An increase in soma cell area following estrogen treatment was observed only in female mPOA enkephalinergic neurons. Taken together, these results indicate a sex difference in total preproenkephalin levels and in estrogenic regulation of preproenkephalin mRNA in the POA of juvenile rats. These results are discussed in relation to the differential role opioids may play in male and female reproductive physiology.


Subject(s)
Enkephalins/genetics , Estrogens/physiology , Preoptic Area/chemistry , Protein Precursors/genetics , Sex Characteristics , Sexual Maturation , Animals , Cell Size/physiology , Enkephalin, Methionine/genetics , Female , Gene Expression Regulation, Developmental , In Situ Hybridization , Male , Neurons/chemistry , Neurons/cytology , Neurons/physiology , Preoptic Area/cytology , Preoptic Area/growth & development , RNA, Messenger/analysis , Rats , Rats, Sprague-Dawley
4.
Cell Mol Neurobiol ; 11(3): 347-56, 1991 Jun.
Article in English | MEDLINE | ID: mdl-1651164

ABSTRACT

1. We have used in situ hybridization techniques to determine the mRNA for (Na + K)ATPase in 20 brain regions from control rats and rats treated with high doses of deoxycorticosterone (DOC). 2. DOC-treated rats developed a salt appetite following the second hormone administration on alternate days and were used after the fourth DOC administration. 3. DOC treatment did not change the number of silver grains/cell deposited in cells from Ca1, CA2, CA3, and CA4 hippocampal subfields, dentate gyrus, cerebral cortex, medial preoptic area (POA), substantia nigra, and periventricular gray matter. 4. Nonsignificant reductions were detected in lateral POA, medial and lateral septum, caudate-putamen, and three amygdaloid nuclei (cortical, basolateral, and central) from DOC-treated rats. 5. Significant reductions were obtained, after DOC administration, in arcuate and ventromedial hypothalamic nuclei and medial and lateral amygdala. 6. The results suggested that regulation of the beta-subunit mRNA of (Na + K)-ATPase may be related to the central actions of mineralocorticoids in the control of salt intake.


Subject(s)
Brain Chemistry/drug effects , Desoxycorticosterone/pharmacology , RNA, Messenger/analysis , Sodium-Potassium-Exchanging ATPase/genetics , Animals , Desoxycorticosterone/administration & dosage , Male , Nucleic Acid Hybridization , RNA, Messenger/genetics , Rats , Rats, Inbred Strains , Sodium/metabolism
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