Hypertrophied Urinary Bladder Research Articles

Features of Reproductive Biology of Papuan Scorpionfish Scorpaenopsis papuensis (Scorpaenidae)

Gonadal structure, oocyte morphology, sperm motility after the activation, and spermatozoa ultrastructure are studied in Papuan scorpionfish Scorpaenopsis papuensis. The oocytes are attached to peduncles originated from ovigerous stroma. The stroma is located in the center of each of two separated ovaries. Based on oocyte diameter distribution, the type of oogenesis is continuous and oocyte deposition is multiple. Spermatozoa at a concentration of 0.005–0.011 × 109 spz/mL are observed in the hypertrophied urinary bladder. Following the activation, spermatozoa obtained from the testes retain high progressive motility for at least 13 min. Based on spermatozoon shape, Sc. papuensis does not notably different from other representatives of the suborder Scorpaenoidei with external fertilization. The nuclear fossa in the spermatozoon nucleus base is absent, and the proximal and distal centrioles are characterized by orthogonal position.

Upregulation of translational machinery in hypertrophied urinary bladder in rat with partial bladder outlet obstruction (704.4)

Partial bladder outlet obstruction (pBOO) causes considerable remodeling of the urinary bladder resulting in bladder organ hypertrophy. The serine/threonine protein kinase Akt serves as a convergent point in signaling networks and plays a critical role in cellular survival and growth. At 2 weeks after surgically induction of pBOO in rat, the phosphorylation (activation) level of the Akt isoform Akt1 was significantly increased in the urinary bladder, whereas the activity of Akt2 was not changed. In the urinary bladder with pBOO, excessive collagen deposition played a significant role in bladder hypertrophy, however, real‐time PCR showed that collagen mRNA level was not changed when compared to control. This was consistent to that the phosphorylation (activation) level of mammalian target of rapamycin (mTOR), p70S6 kinase (p70S6K), and 4E‐BP1, a protein synthesis pathway downstream of Akt1, were increased in pBOO bladder. The increases in protein synthesis also resulted in detrusor smooth muscle cellular hypertrophy examined by an increase in the relative level of α‐smooth muscle actin against nuclear protein histone H3. These results suggest that an increased protein synthesis regulated by Akt1‐mediated translational machinery may underlie pBOO‐induced bladder hypertrophy resulting from excessive collagen deposition and detrusor smooth muscle cellular hypertrophy.Grant Funding Source: DK077917

Transition to viviparity in the order Scorpaeniformes: Brief review

Among teleost percoid fishes (Percomorpha), the subordes Scorpaenoidei (Scorpaeniformes) and Zoarcoidei (Perciformes) are of particular interest due to the presence of intermediate stages between oviparity and viviparity in several species. We analyze the features of reproductive biology in the fishes of the suborder Scorpaenoidei, including morphology of the urogenital system, gametogenesis, gamete ultrastructure, and embryonic development. The new materials are represented for three tropical coral reef fish species with external insemination from the family Scorpaenidae (Scorpaenopsis possi, Sebastapistes cyanostigma, and Dendrochirus zebra). In particular, a hypertrophied urinary bladder used for storage of mature sperm for insemination of pelagic egg clutch is described in the males. Evolutionary transition to viviparity within the family Sebastidae is discussed. Alternative reproductive strategies are registered in viviparous fishes from the suborders Scorpaenoidei and Zoarcoidei. They are connected with the production of a large number of morphologically weakly developed larvae and a small number of individuals at the juvenile state, respectively.

Features of reproductive biology in two tropical fish species from the family Scorpaenidae

Composition of the urogenital system, oocyte development, gamete morphology, and features of embryonic development are described in Scorpaenopsis possi and Sebastapistes cyanostigma (Scorpaenidae) from the Nha Trang Bay, the South China Sea (Vietnam). In males of both species, paired spermiducts enter into the anterior dorsal part of the hypertrophied urinary bladder containing mature sperm. The duration of progressive movements of spermatozoa obtained from the testes and urinary bladder is 5–6 and 12–15 min after activation, respectively. Ovulated oocytes possess oval shapes, they are transparent and without oil droplets. The oocytes are embedded into the floating gelatinous matrix. Insemination of the eggs in nature is apparently external. The embryos of S. cyanostigma hatch at a more advanced morphological condition in comparison to the embryos of Sc. possi. The features of reproductive biology are discussed in the context of the evolution of viviparity within the family.

Altered expression of thin filament‐associated proteins in hypertrophied urinary bladder smooth muscle

Obstruction of the urinary bladder outlet induces detrusor smooth muscle (DSM) hypertrophy. The goal of this study was to determine whether the composition of thin filament-associated proteins, known to play important roles in cytoskeletal structure and/or the regulation of contraction, is altered in DSM during hypertrophy. DSM hypertrophy was induced in male rabbits by partial ligation of the urethra. Sham-operated rabbits served as a control. Reverse transcriptase-polymerase chain reaction (RT-PCR) and real-time PCR revealed a significant increase in the expression of mRNAs for basic (h1) calponin (CaP), and alpha-isoform of tropomyosin (Tm) in hypertrophied DSM compared to controls. Western blotting and two-dimensional (2-D) gel electrophoresis showed enhanced expression of these proteins and also a significant increase in the expression of beta-non muscle and gamma-smooth muscle actin in the DSM from obstructed bladders, while alpha-actin remained constant. Enhanced expression of these proteins in the DSM from obstructed bladders was confirmed by immunofluorescence microscopy. Double immunostaining with Cap/Tm and alpha/beta-actin-specific antibodies showed co-localization of these proteins in myocytes. Colocalization of smooth muscle specific myosin and CaP to cytoplasmic filaments in cells dissociated from the hypertrophied DSM indicated that these cells are differentiated smooth muscle cells. The change in the isoforms of actin, Cap, and Tm may be part of the molecular mechanism for bladder compensation in increased urethral resistance.

Generation of a cell line with smooth muscle phenotype from hypertrophied urinary bladder.

We have established a cell line from hypertrophied rabbit urinary bladder smooth muscle (SM) that stably expresses SM myosin (SMM). These cells, termed BSM, are spindle shaped and form swirls, similar to the "hills and valleys" described for cultured aortic SM cells. Western blotting revealed that BSM expresses the amino-terminal SMM heavy chain isoform SM-B, the carboxy-terminal SM1 and SM2 isoforms, and SM alpha-actin. In addition, they express cGMP-dependent protein kinase G, made by contractile SM cells in vitro but not by noncontractile cells synthesizing extracellular matrix. Immunofluorescence studies indicate a homogeneous population of cells expressing alpha-actin and SMM, including the SM-B isoform, and karyotyping demonstrates a stable 4N chromosomal pattern. These cells also express calcium-dependent myosin light chain kinase and phosphatase activity and contract in response to the muscarinic agonist bethanechol. To our knowledge, BSM is the first visceral SM cell line that expresses the SM-B isoform and might serve as a useful model to study the transcriptional regulation of tissue-specific SMM isoforms in differentiation and pathological SM.

Structure and mechanics of growing arterial microvessels from hypertrophied urinary bladder in the rat

Rat bladder hypertrophy, induced by a partial ligation of the urethra, was used to study the accompanying changes of microvascular smooth muscle mechanics, pharmacology and morphology. A segment of a microarterial vessel to the bladder was taken from a defined anatomical location and studied in a wire myograph in vitro at the length for maximal isometric force development (Lmax). After 10 days of ligation, bladder hypertrophy resulted in a microvascular growth response compared to non-operated controls which was characterized by (i) an increase of the calculated diameter at Lmax from 134 +/- 5 microns to 222 +/- 19 microns; (ii) an increase of the media thickness from 22.4 +/- 1.9 microns to 32.2 +2- 3.0 microns; (iii) an increase of the active tension from 1.42 +/- 0.28 mN/mm to 3.06 +/- 0.33 mN/mm; (iv) no change of the wall/lumen ratio (from 0.83 +/- 0.10 to 0.79 +/- 0.15). Normalized length/force relations (active, passive and total) did not differ significantly between microarteries from control and hypertrophic bladders. Microvascular smooth muscle growth was also associated with a decreased sensitivity to K(+)-induced depolarization and an increased sensitivity to alpha 1-adrenergic stimulation. No differences were noted regarding the Ca2+ sensitivity of force during K(+)-induced depolarization. The results suggest that microvascular growth (1) is immediately and positively influenced by the organ growth; (2) results in a functional resetting of the microvascular segments towards larger diameters without gross morphological or mechanical alterations; and (3) is accompanied by pharmacological alterations of the smooth muscle reactivity.

Alterations in the expression of the beta-cytoplasmic and the gamma-smooth muscle actins in hypertrophied urinary bladder smooth muscle.

The obstruction of the bladder outlet induces a marked increase in bladder mass, and this is accompanied by reduced contractility of bladder smooth muscle and alteration in the cellular architecture. In this study, we show that the composition of various isoforms of actin, a major component of the contractile apparatus and the cytoskeletal structure of smooth muscle, is altered in response to the obstruction-induced bladder hypertrophy. Northern blot analysis of the total RNA isolated from hypertrophied urinary bladder muscle, using a cDNA probe specific for smooth muscle gamma-actin, shows over 200% increase in the gamma-actin mRNA. However, the estimate of the amount of actin from the 2D gel reveals only a 16% increase in gamma-actin, since the 2D gel electrophoresis does not distinguish gamma-smooth muscle actin from gamma-cytoplasmic actin. The bladder smooth muscle alpha-actin and the smooth muscle alpha-actin mRNA are not altered in response to the hypertrophy. The obstructed bladder also reveals a decrease in the beta-cytoplasmic actin (37%) and a concomitant diminution in the beta-cytoplasmic actin mRNA (29%). Hence, the composition of the actin isoforms in bladder smooth muscle is altered in response to the obstruction-induced hypertrophy. This alteration of the actin isoforms is observed at both the protein and mRNA levels.

Effect of outlet obstruction on pyruvate metabolism of the rabbit urinary bladder.

Bladder function is dependent upon cellular metabolism of substrates and the adequate generation of high-energy phosphate compounds. Partial outlet obstruction induces a marked decrease in bladder function which is associated with a significant decrease in the oxidative metabolism of glucose. The current investigation was designed to determine whether the time course of the decrease in mitochondrial oxidation in the hypertrophied urinary bladder is similar to the time course of the contractile dysfunction observed. In these studies we determined: 1) the rate of 14C-pyruvate metabolism to 14CO2 in control and obstructed tissue (1, 3, 5 and 7 days), and 2) the mitochondrial enzymatic activities of malate dehydrogenase and citrate synthase. The results can be summarized as follows: 1) The rate of pyruvate metabolism decreases by over 50% within one day following partial outlet obstruction, and remains at this level for the seven day period of study. 2) Kinetic analysis demonstrates that the change in enzymatic activity is related to a decrease in Vmax; the Kd for pyruvate is similar for control and after all time periods of obstruction. 3) The enzymatic activity of malate dehydrogenase and citrate synthase is reduced by over 50% within one day following partial obstruction, and remains at this level throughout the 7 day study period. These metabolic results correlate in time and duration with the decreased ability of the bladder to empty following partial outlet obstruction.

Force development in smooth muscle strips of the hypertrophied urinary bladder of the rat after autonomic decentralization.

Active length-tension relations for muscle strips of decentralized bladders differed from those of controls when comparisons were based on length in situ, but not when comparisons were based on lengths relative to optimum lenght for force development. The decentralized bladder behaved similarly to the denervated bladder, thus indicating that the presence of nerves was of no importance for the force production of directly stimulated muscle cells in the hypertrophied bladder.

Changes in noradrenaline sensitivity and morphology of arterial resistance vessels during development of high blood pressure in spontaneously hypertensive rats.

Changes in noradrenaline sensitivity and morphology of arterial resistance vessels during development of high blood pressure in spontaneously hypertensive rats.