Effects of short‐term partial bladder outlet obstruction on the rabbit detrusor: An ultrastructural study

It has been shown previously that partial bladder outlet obstruction in the rabbit results in changes in detrusor contractility and biochemical profile [Malkowicz et al., 1986]. The present study was conducted in the same animal model to define the nature and evolution of concomitant structural neuromuscular changes in the detrusor, as the basis for its altered function following partial outlet obstruction. Twenty‐five New Zealand White rabbits, including three normal controls, were used. The bladder was excised in 15 rabbits at various intervals 1–14 days postoperatively. In the remaining seven rabbits, the obstruction was relieved after 7 days, and the bladders were excised 14 or 28 days later. Multiple samples of the midbody detrusor were obtained from each specimen and processed for electron microscopy by standard techniques. Changes were observed in the smooth muscle, interstitial, and neural compartments. The muscular changes included a combination of muscle cell degeneration and regeneration, and widening of intercellular spaces with deposition of basal lamina‐like material. Both degenerative and regenerative muscle cell profiles were uncommon in the control and 1 day obstructed samples, frequent in the 3–7 day obstructed samples, and less frequent in the 14 day obstructed samples. The spaces between individual muscle cells appeared to become increasingly wider in the 3–14 day obstructed samples. The ultrastructure of smooth muscle in samples from both deobstructed groups was similar to controls, except for thickened basal laminae of muscle cells and consistently widened intercellular spaces. The interstitial compartment appeared to become progressively exaggerated with increasing deposits of collagen and elastin in the 3–14 day obstructed samples; these changes persisted in samples from both deobstructed groups. In regard to the neural compartment, degeneration of both cholinergic and adrenergic nerves with loss of neuroeffector junctions was observed in the 3–7 day obstructed samples; axonal regeneration was seen with re‐establishment of the junctions in the 14 day obstructed and both deobstructed groups. It is concluded that partial bladder outlet obstruction in the rabbit results in partially reversible neuromuscular changes in the detrusor, which can explain the resultant alterations in detrusor contractility and biochemical profile.

[1]  A. Wein,et al.  Acute biochemical and functional alterations in the partially obstructed rabbit urinary bladder. , 1986, The Journal of urology.

[2]  P. Biancani,et al.  Effect of vesical outlet obstruction on detrusor contractility and passive properties in rabbits. , 1986, The Journal of urology.

[3]  J. Woessner,et al.  Content of the collagen and elastin cross-links pyridinoline and the desmosines in the human uterus in various reproductive states. , 1985, American journal of obstetrics and gynecology.

[4]  A. Wein,et al.  Recovery from short-term obstruction of the rabbit urinary bladder. , 1985, The Journal of urology.

[5]  B. Uvelius,et al.  Collagen content in the rat urinary bladder subjected to infravesical outflow obstruction. , 1984, The Journal of urology.

[6]  A. Elbadawi Ultrastructure of vesicourethral innervation. I. Neuroeffector and cell junctions in the male internal sphincter. , 1982, The Journal of urology.

[7]  R. Cortivo,et al.  Elastin and collagen in the normal and obstructed urinary bladder. , 1981, British journal of urology.

[8]  A. Dvorak,et al.  Crohn's disease: transmission electron microscopic studies. III. Target tissues. Proliferation of and injury to smooth muscle and the autonomic nervous system. , 1980, Human pathology.

[9]  H. Koch,et al.  Electron microscopic studies on the small intestine of rats after mechanical intestinal obstruction , 1979, Virchows Archiv. B, Cell pathology including molecular pathology.

[10]  R. Cortivo,et al.  The elastic tissue of the adult dilated ureter. , 1977, British journal of urology.

[11]  G. Gabella,et al.  Synthesis of collagen by smooth muscle in the hyertrophic intestine. , 1977, Quarterly journal of experimental physiology and cognate medical sciences.

[12]  Gerrity Rg,et al.  The aortic tunica media of the developing rat. II. Incorporation by medial cells 3-H-proline into collagen and elastin: autoradiographic and chemical studies. , 1975 .

[13]  R. Cloutier Intestinal smooth muscle response to chronic obstruction : possible applications in jejunoileal atresia. , 1975, Journal of pediatric surgery.

[14]  J. Emery,et al.  A classification and quantitative histological study of abnormal ureters in children. , 1974, British journal of urology.

[15]  J. Tighe,et al.  The damaged human detrusor: functional and electron microscopic changes in disease. , 1973, British journal of urology.

[16]  R. D. Harkness,et al.  Collagen formation and changes in cell population in the rat's uterus after distension with wax. , 1968, Quarterly journal of experimental physiology and cognate medical sciences.

[17]  R. Ross,et al.  FINE STRUCTURAL CHANGES IN UTERINE SMOOTH MUSCLE AND FIBROBLASTS IN RESPONSE TO ESTROGEN , 1967, The Journal of cell biology.

[18]  D. Pease,et al.  REGENERATIVE CHANGES IN RAT DORSAL ROOTS FOLLOWING WALERIAN DEGENERATION. , 1963, Journal of ultrastructure research.

[19]  R. D. Harkness,et al.  The distribution of the growth of collagen in the uterus of the pregnant rat , 1956, The Journal of physiology.

[20]  W. S. Root,et al.  Effect of parasympathetic denervation on feline bladder function. , 1951, The American journal of physiology.

[21]  A. Wein,et al.  Quantitative analysis of intercellular changes in the short‐term partially obstructed rabbit detrusor , 1989 .

[22]  A. Wein,et al.  Morphometric analysis of muscle cell changes in the short‐term partially obstructed rabbit detrusor , 1989 .

[23]  A. Elbadawi,et al.  Morphometry of the obstructed detrusor: II. Principles of a comprehensive protocol , 1989 .

[24]  A. Elbadawi,et al.  Intrinsic neuromuscular defects in the neurogenic bladder: VIII. Effects of unilateral pelvic and pelvic plexus neurectomy on ultrastructure of the feline bladder base , 1988 .

[25]  B. Uvelius,et al.  Changes in the nervous control of the rat urinary bladder induced by outflow obstruction , 1987 .

[26]  A. Elbadawi,et al.  Intrinsic neuromuscular defects in the neurogenic bladder. 1. Short‐term ultrastructural changes in muscular innervation of the decentralized feline bladder base following unilateral sacral ventral rhizotomy , 1984 .

[27]  A. Elbadawi,et al.  Intrinsic neuromuscular defects in the neurogenic bladder. III. Transjunctional, short‐ and long‐term ultrastructural changes in muscle cells of the decentralized feline bladder base following unilateral sacral ventral rhizotomy , 1984 .

[28]  B. Uvelius,et al.  Smooth muscle cell hypertrophy and hyperplasia in the rat detrusor after short-time infravesical outflow obstruction. , 1984, The Journal of urology.

[29]  Gosling Ja,et al.  Structural changes associated with obstruction of the urinary tract: A comparison between upper and lower systems. , 1981 .

[30]  C. Chiou Neuromuscular blocking actions of (4,4'-biphenylene-bis-(2-oxoethylene))-bis-2-ethoxyethyl) methylammonium bromide) 'DEO'. , 1974, Pharmacology.

[31]  L. Brent THE RESPONSE OF SMOOTH MUSCLE CELLS IN THE RABBIT COLON TO ANAL STENOSIS: A PRELIMINARY REPORT , 1973, Pathology.

[32]  J. Downie,et al.  The relationship between elastin and an acidic protein in mammalian uterus. , 1973, Connective tissue research.

[33]  P. Dyck,et al.  Electron microscopic observations on degeneration and regeneration of unmyelinated fibres. , 1972, Brain : a journal of neurology.