SUMMARY:Disturbances of the urinary bladder functions are common in the elderly people particularly women. So, it was the aim of the present work to detect the age-associated changes in the urinary bladder that might play a role in the bladder dysfunctions. Twenty albino rats were used in the present work. They were divided into two equal groups, each consisted of ten rats. The first group included the adult rats (aged 3 months) and served as control group, while the second group was the senile rats (aged 24 months). Specimens of the urinary bladder were taken, processed and examined using the light microscope (LM) and the scanning electron microscope (SEM).Light microscopic examination of the urinary bladder of the aged rats showed marked mucosal damage, ranging from degeneration of the epithelial cells to complete denudation of the mucosa with exposed lamina propria. Cellular infiltration and increased dilated and congested blood vessels of the lamina propria were also encountered. The smooth muscle cells of the muscularis showed variable degrees of degeneration with wide separation of the muscle bundles. Massive increase in collagen fibres deposition was detected in the lamina propria, muscle layer and adventitia. SEM examination revealed loss of the polygonal cell pattern appearance of the superficial epithelial cells and an increase in the collagen fibres in all the portions of the mucosa, It was concluded that the observed age-related changes might be contributing factors in the urinary bladder disturbances in elderly population.
KEY WORDS: Urothelium; Urinary mucosa; Urinary muscularis; Bladder dysfunction.Department of Anatomy, College of Medicine, King Faisal University, Dammam, Saudi Arabia. 310 considered as a control, while the second group constituted the senile rats (aged 24 months). The animals were sacrificed by decapitation. The anterior abdominal wall was opened and the urinary bladder was excised.Light microscopic study. Immediately following excision, the urinary bladder was fixed in 10% formal saline solution. Specimens from the anterior wall of the bladder were processed for paraffin blocks and sectioned at a thickness of 7µm. These sections were stained by routine hematoxylin and eosin and Masson's trichrome stain (Drury & Wallington, 1983).Scanning electron microscopic study. Strips of 3 -5 mm from the anterior wall of the urinary bladder were immediately fixed in 2% paraformaldehyde and 2.5% glutaraldehyde in 0.1 M phosphate buffer for 24 h; fixation and washing were carried out at 4ºC. The tissues were then dehydrated through ascending grades of ethanol and substituted with isomylacetate. The pieces of the urinary bladder were dried at critical point using liquid carbon dioxide (CO 2 ). The tissue specimens were mounted on stubs with aluminum conducting tape and sputter coated with 20 nm layer of gold in JFC ion. The specimens were examined and photographed with XL 30 scanning electron microscope (Philips) operated at 30 KV (Robinson et al., 1987).
RESULTSGroup I (Adult female rats; con...