Reduced flow after tubularized incised plate urethroplasty--increased fibrogenesis, elastin fiber loss or neither?

PURPOSE: Low urinary flow rates are common after tubularized incised plate urethroplasty but the etiology remains unclear and may be related to low urethral compliance due to abnormal collagen concentrations and/or fewer elastic fibers in the healed urethral plate. We hypothesized that inserting a preputial mucosal graft over the dorsal raw area after the midline incision may avoid scarring and improve urethral compliance. MATERIALS AND METHODS: Adult rabbits were submitted to tubularized incised plate urethroplasty with or without inlay preputial graft according to a previously described protocol. Tissular concentrations of collagens I, III, IV, VI, VIII and XIII were measured. Histomorphometric analysis was used to quantify elastic fibers in the urethra. Tubularized incised plate urethroplasty with and without inlay preputial graft was compared to normal rabbit urethras (controls). RESULTS: mRNA concentrations for collagens I, II and XIII were similar between controls and operated rabbits. The proportions between collagens I and III were 1.05, 0.87 and 1.21, respectively, in controls and animals undergoing tubularized incised plate urethroplasty with and without inlay preputial graft. mRNA concentrations for collagen IV and collagens VI/VIII tended to be higher and lower, respectively, in the operated urethras, despite showing statistical significance only for collagen VIII in animals undergoing tubularized incised plate urethroplasty with inlay preputial graft vs controls (p=0.02). The operated animals did not demonstrate a reduced number of elastic fibers in the urethral tissues compared to controls. CONCLUSIONS: Elastic fiber number and distribution were similar between tubularized incised plate urethroplasty cases and controls, suggesting that decreased concentrations of elastic fibers do not explain the reduced urethral compliance after tubularized incised plate urethroplasty. The raw area determined by the dorsal urethral incision regenerated after standard tubularized incised plate urethroplasty, while cicatrization with fibrosis occurred in correspondence to the grafted areas after tubularized incised plate urethroplasty with inlay preputial graft.

Granulomatous orchitis in a pre-pubertal school-aged child: differential diagnosis dilemmas.

A 6-year-old male presented with testicular growth and persistent chronic orchiepididymitis with high inflammatory markers (C reactive protein and erythrocyte sedimentation rate). Biopsies of the testes and epididymides showed bilateral epididymal and testicular granulomata, testicular fibrosis and chronic inflammatory infiltration, and the histological diagnosis was granulomatous orchitis. The symptoms receded with oral corticosteroids. Although rare, granulomatous orchitis is a possible diagnosis in children presenting testicular enlargement. It is important to differentiate it from testicular tumors (if necessary with testicular biopsy) and to investigate its association with systemic vasculitis and infectious diseases.

Merozoite release from Plasmodium falciparum-infected erythrocytes involves the transfer of DiIC16 from infected cell membrane to Maurer's clefts.

Merozoite release from infected erythrocytes is a complex process, which is still not fully understood. Such process was characterised at ultra-structural level in this work by labelling erythrocyte membrane with a fluorescent lipid probe and subsequent photo-conversion into an electron-dense precipitate. A lipophilic DiIC(16) probe was inserted into the infected erythrocyte surface and the transport of this phospholipid analogue through the erythrocyte membrane was followed up during 48 h of the asexual erythrocyte cycle. The lipid probe was transferred from infected erythrocyte membranes to Maurer's clefts during merozoite release, thereby indicating that these membranes remained inside host cells after parasite release. Fluorescent structures were never observed inside infected erythrocytes preceding merozoite exit and merozoites released from infected erythrocyte were not fluorescent. However, specific precipitated material was localised bordering the parasitophorous vacuole membrane and tubovesicular membranes when labelled non-infected erythrocytes were invaded by merozoites. It was revealed that lipids were interchangeable from one membrane to another, passing from infected erythrocyte membrane to Maurer's clefts inside the erythrocyte ghost, even after merozoite release. Maurer's clefts became photo-converted following merozoite release, suggesting that these structures were in close contact with infected erythrocyte membrane during merozoite exit and possibly played some role in malarial parasite exit from the host cell.

Histología y morfometría del ojo del pez dulceacuícola Paracheirodon axelrodi (Characiformes: Characidae)

Histology and morphometry of the eye in the freshwater Paracheirodon axelrodi (Characiformes: Characidae). The visual system of Teleost fishes has a wide range of adaptations. The eye has suffered modifications, mainly towards better sensitivity and visual resolution according to specific environmental conditions. In that way, this organ is so important for survival. In spite of being the most commercialized Orinoquía species, and one of the most important ornamental fish worldwide, there are almost no studies on the communication systems of P. axelrodi (including vision). We studied the eye in ten individuals of P. axelrodi, with a mean total length of 2.7 cm (SD= 0.2, n= 20). We measured eye relative size (TRO) after sacrifice. Heads were processed for hematoxylin-eosin, and 8 μm thick sections were obtained. Images were digitalized for histological identification and morphometrics. The relation between TRO and body length was 9.8% (SD= 1.1, n= 20); lens was spherical with a relative size of 64.3% (SD= 4.9, n= 20). Rete mirabilis choroid was composed mainly by capillaries, while sclera was composed of cartilaginous tissue. Retina with eight layers and two membranes. An areae centrales was observed in the posterior retina. Iris covered by a simple cubic epithelium. Cornea of endothelial tissue with two membranes. Pupil almost circular, with a naso-caudal elongation. Measures of retina thickness were as follows: lateral retina 144.5 μm (SD= 5.4, n= 20), temporal retina 210.4 μm (SD= 14.8, n= 20). Lens measurements were: dorso- ventral 759.6 μm (SD= 31.7, n= 20), antero-posterior 763.4 μm (SD= 30.7, n= 20). Cornea thickness was 27.6 μm (SD= 4.3, n= 20); iris thickness was 18.9 μm (SD= 1.9, n= 20); rete mirabilis choroid 22.2 μm (SD= 3.2, n= 20) and sclera: 15.9 μm (SD= 1.2, n= 20). This species has a typical Teleost eye conformation. The retina was thicker in the posterior area, probably related to the presence of neuron groups. This modification allows for a better sharpness and visual resolution. The TRO, areae centrales in the retina, and thin cornea, suggests the need of a well developed visual system resulting from a predatory diet. Rev. Biol. Trop. 57 (4): 1107-1118. Epub 2009 December 01.

El pez dulceacuícola P. axelrodi es de gran importancia comercial en la Orinoquía Colombiana y a nivel mundial, pero carece de estudios acerca de su visión. Se utilizaron diez individuos, con longitud total promedio de 2.7 cm (SD= 0.2, n= 20). Se realizaron cortes a 8 μm y se tiρeron con H-E. El tamaρo relativo del ojo es 9.8% (SD= 1.1, n= 20); el cristalino tiene un tamaρo relativo de 64.3% (SD= 4.9, n=20). Una esclerótica con tejido cartilaginoso. La retina está constituida por ocho capas y dos membranas, hay areae centrales en la zona posterior, por lo tanto tiene mayor espesor que la zona lateral. El espesor promedio de las estructuras es: retina lateral: 144.5 μm (SD= 5.4, n= 20), retina temporal: 210.4 μm (SD= 14.8, n= 20); cristalino (esfιrico): dorso-ventral 759.6 μm (SD= 31.7, n= 20) y antero- posterior 763.4 μm (SD= 30.7, n= 20) y cσrnea: 27.6 μm (SD= 4.3, n= 20). El tamaρo relativo del ojo, relacionado con la presencia de areae centrales y una córnea delgada, muestra las necesidades visuales del neón cardenal (cazador) para adaptarse al hábitat, lo que hace necesario tener un sistema visual desarrollado que le permita tener mejor sensibilidad y resolución visual.

[Histology and morphometry of the in the freshwater Paracheirodon axelrodi (Characiformes: Characidae)]. / Histología y morfometría del ojo del pez dulceacuícola Paracheirodon axelrodi (Characiformes: Characidae).

The visual system of Teleost fishes has a wide range of adaptations. The eye has suffered modifications, mainly towards better sensitivity and visual resolution according to specific environmental conditions. In that way, this organ is so important for survival. In spite of being the most commercialized Orinoquia species, and one of the most important ornamental fish worldwide, there are almost no studies on the communication systems of P. axelrodi (including vision). We studied the eye in ten individuals of P. axelrodi, with a mean total length of 2.7 cm (SD = 0.2, n = 20). We measured eye relative size (TRO) after sacrifice. Heads were processed for hematoxylin-eosin, and 8 microm thick sections were obtained. Images were digitalized for histological identification and morphometrics. The relation between TRO and body length was 9.8% (SD= 1.1, n= 20); lens was spherical with a relative size of 64.3% (SD = 4.9, n = 20). Rete mirabilis choroid was composed mainly by capillaries, while sclera was composed of cartilaginous tissue. Retina with eight layers and two membranes. An areae centrales was observed in the posterior retina. Iris covered by a simple cubic epithelium. Cornea of endotelial tissue with two membranes. Pupil almost circular, with a naso-caudal elongation. Measures of retina thickness were as follows: lateral retina 144.5 microm (SD = 5.4, n = 20), temporal retina 210.4 microm (SD = 14.8, n = 20). Lens measurements were: dorso-ventral 759.6 microm (SD = 31.7, n = 20), antero-posterior 763.4 microm (SD = 30.7, n = 20). Cornea thickness was 27.6 microm (SD = 4.3, n = 20); iris thickness was 18.9 microm (SD = 1.9, n = 20); rete mirabilis choroid 22.2 microm (SD = 3.2, n = 20) and sclera: 15.9 microm (SD = 1.2, n = 20). This species has a typical Teleost eye conformation. The retina was thicker in the posterior area, probably related to the presence of neuron groups. This modification allows for a better sharpness and visual resolution. The TRO, areae centrales in the retina, and thin cornea, suggests the need of a well developed visual system resulting from a predatory diet.

A quantitative method for analysing neuron networks marked by acetylcholinesterase histochemistry / Un método cuantitativo para analizar redes neuronales marcadas por histoquimica para acetilcolinesterasa

El análisis cualitativo de las redes neuronales por histoquímica enzimática se usa comúnmente en los estudios morfológicos tradicionales. Una limitante de este tipo de estudios consiste en la dificultad de obtener resultados cuantitativos. Este artículo presenta dos técnicas originales de procesamiento de imágenes para realizar estudios cuantitativos y un análisis comparativo entre ellas. Los resultados preliminares presentados permiten verificar la utilidad de la metodología aplicada

A quantitative method for analysing neuron networks marked by acetylcholinesterase histochemistry.

Enzyme histochemistry is frequently used in classical morphological studies for the qualitative analysis of neuronal networks. However, this procedure does not readily provide quantitative results. Two new alternative approaches based on digital image processing techniques were explored and the data quality compared. The preliminary results explored the feasibility of these approaches in the applied setting.

ATPasa de calcio en el sistema nervioso / Calcium ATPase in the nervous system

La bomba de calcio es una proteína integral de la membrana que regula el calcio libre citoplasmático en concentraciones menores de 0,1 mM. En la mayoría de las células eucarióticas está ubicada en la membrana, en el plasmalema o en organelos como el retículo sarcoendoplásmico y los calciosomas. Su actividad está dada por la hidrólisis de ATP, la concentración del ion en el citoplasma y por otros factores que regulan como la calmodulina, los fosfolípidos y las proteínas - cinasas. Por diferentes métodos, se ha detectado la ATPasa de calcio y su actividad en el tejido nervioso central y periférico, como en otros tejidos