PubMed · 13952001
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L HAJDU, Z ZSIGMOND. 1963. [Experiences with electric conization based on 471 cases].. https://pubmed.ncbi.nlm.nih.gov/13952001/
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BACKGROUND: The objective of the investigation was to demonstrate the presence of voltage-dependent Ca2+ current in human prostate smooth muscle cells and to determine their biophysical characteristics. METHODS: Prostate smooth muscle cells were isolated from biopsy samples of human prostates obtained from prostatectomy specimens or TURP chips. Electrophysiological recordings were made under current- or voltage-clamp using patch-type electrodes. RESULTS: The average resting potential of prostate myocytes was 63 +/- 11 mV and action potentials (APs) could be elicited when K+ currents were blocked. With K-filled electrodes inward current was followed by a large outward component. When K+ currents were blocked a large Ca2+-sensitive inward current was measured. The inward current could be divided into two components, a fraction blocked by 30 microM verapamil and another by 20 microM NiCl2. CONCLUSIONS: Based on the sensitivity to antagonists and holding potential both L-type and T-type Ca2+ channels were identified in human prostate smooth muscle.
The cause of interstitial cystitis (IC) is still unknown. Several features suggest that it may be an infectious disease and it has compelling similarities to chronic gastritis. The identification of Helicobacter pylori as the cause of chronic gastritis focused attention on this organism. Many studies have been done investigating the role of H. pylori in the etiology of IC. Previous studies mostly determined the presence of H.pylori with antibodies in the serum samples of IC patients, but these methods may lead to false positive or negative results. We therefore investigated the presence of H.pylori in bladder biopsy specimens by using polymerase chain reaction (PCR), which is accepted as the most sensitive and specific test for detecting this organism. A total of 32 patients with IC were enrolled into the study. The PCR assay was performed on cold cup bladder biopsies of IC patients. Both positive and negative controls were included in each set of PCR reactions. Gastric biopsy specimens of peptic ulcer patients with proven H. pylori infection were used as positive controls. Bladder biopsies of all IC patients were negative for H. pylori DNA. PCR showed the presence of H. pylori in the positive controls in each cycle demonstrating that the PCR assay was working properly. Thus, there is no evidence that IC is the result of H. pylori infection. This study does not negate the possibility that other infectious agents may play a role in the etiology of IC.
For chronic maxillary sinusitis, the most popular surgical approach for treatment is endoscopic sinus surgery (ESS). After these operations, however, it is not clear how well the surgery restores the normal mucociliary function. We examined the mucociliary clearance (MCC) in maxillary sinuses in chronic sinusitis before ESS and 6 months after the operations. The correlation of histology to MCC was also studied. Measurements of the mean residual mucociliary clearance (MCC) of maxillary sinuses was studied pre- and postoperatively with an isotope method. Biopsies taken during ESS and 6 months postoperatively were studied by electron microscopy (EM). Preoperative residual MCC from the maxillary sinuses was 77+/-26% (mean+/-SD). Six months postoperatively, residual MCC was 70+/-22%, only slightly better than preoperatively. Residual MCC was considered good (< or = 50%) in 12% of sinuses preoperatively and in 20% postoperatively. In preoperative sinuses, 14% did not show any mucociliary clearance compared to 11% postoperatively. As a single EM finding, metaplasia gave the poorest MCC (91%) and microvilli the best (68%). Mucociliary function in maxillary sinusitis remains poor even 6 months postoperatively, with many pathological findings still visible in the sinus epithelium. MCC correlates well with the histology of the mucosa. Surgery does not significantly improve the mucociliary function of sinus mucosa in chronic maxillary sinusitis.