Ultrastructural study of electron dense deposits in renal tubular basement membrane: prevalence and relationship to epithelial atrophy.

This study reports the prevalence of immune deposits associated with the proximal and distal tubules in a series of routine renal biopsies received in our department during a single calendar year. From 87 cases, 65 (74%) were found to have glomerular immune deposits by immunofluorescence. Tubular immune deposits were found in 12 cases (18%), 3 of which had no glomerular deposits. By transmission electron microscopy (EM), 58 cases (66%) were found to have deposits of granular or vesicular material associated with the tubular basement membranes (TBM). Finely granular electron dense deposits appeared to correspond to the immune deposits seen by immunofluorescence microscopy (IF) and may be a sensitive marker of immune deposition.

Quantum dot immunocytochemical localization of somatostatin in somatostatinoma by Widefield Epifluorescence, super-resolution light, and immunoelectron microscopy.

Quantum dot nanocrystal probes (QDs) have been used for detection of somatostatin hormone in secretory granules of somatostatinoma tumor cells by immunofluorescence light microscopy, super-resolution light microscopy, and immunoelectron microscopy. Immunostaining for all modalities was done using sections taken from an epoxy resin-embedded tissue specimen and a similar labeling protocol. This approach allowed assessment of labeling at light microscopy level before examination at super-resolution and electron microscopy level and was a significant aid in interpretation. Etching of ultrathin sections with saturated sodium metaperiodate was a critical step presumably able to retrieve some tissue antigenicity masked by processing in epoxy resin. Immunofluorescence microscopy of QD-immunolabeled sections showed somatostatin hormone localization in cytoplasmic granules. Some variable staining of tumor gland-like structures appeared related to granule maturity and dispersal of granule contents within the tumor cell cytoplasm. Super-resolution light microscopy demonstrated localization of somatostatin within individual secretory granules to be heterogeneous, and this staining pattern was confirmed by immunoelectron microscopy.

Calcification of intraocular hydrogel lens: evidence of dystrophic calcification.

PURPOSE: To report and describe the surface calcification of three cases of implanted intraocular hydrogel lens. METHODS: Three surgically extracted hydrogel intraocular lenses were studied by light and transmission electron microscopy as well as by energy dispersion X-ray microanalysis. RESULTS: The lens surfaces were covered by granular deposits of calcium phosphate, clearly delineated by von Kossa and alizarin stains for calcium. Transmission electron microscopy showed the deposits to be located within the superficial lens material to a depth of 7 microm and to be associated with what appear to be traces of cellular material including basement membrane and plasmalemma. To the authors' knowledge there has been only one other transmission electron microscopic study. Energy dispersion X-ray microanalysis showed the deposits to contain calcium and phosphorous in all cases. CONCLUSIONS: This study confirms and extends the previous reports of five cases of calcification of hydrogel intraocular lenses. The exact mechanism of calcification remains obscure but evidence suggesting cell-mediated dystrophic calcification of the lens surface is presented. Further study is required to monitor the incidence and development of this phenomenon.

Vasopeptidase inhibition reverses myocardial vasoactive intestinal peptide depletion and decreases fibrosis in salt sensitive hypertension.

We have shown previously that the concentration of Vasoactive Intestinal Peptide (VIP) in the heart is inversely correlated with the degree of fibrosis in a number of experimental models of early myocardial fibrosis. Vasopeptidase inhibition and angiotensin converting enzyme inhibition both decrease myocardial fibrosis. In this study, we sought to determine whether this myocardial protective effect might reflect increased VIP concentrations in the heart. We compared the effects of 4 weeks treatment of the vasopeptidase inhibitor omapatrilat and the angiotensin converting enzyme inhibitor enalapril on the degree of fibrosis and the concentration of VIP in the heart in salt sensitive hypertension induced by treatment with L-nitro-omega-methylarginine (L-NAME). Systolic blood pressure decreased in both treatment groups compared with control (omapatrilat P<0.005; enalapril P<0.001). Myocardial fibrosis was less for omapatrilat than control (P<0.0005) and enalapril (P<0.0005) groups. Myocardial VIP was greater in omapatrilat than in controls (P<0.005) and enalapril-treated rats (P<0.05). We conclude that vasopeptidase inhibition exerts a greater myocardial protective effect than angiotensin converting enzyme inhibition. Further, this myocardial protective effect is associated with increased VIP in the heart suggesting a pathogenetic role for VIP depletion in the development of fibrosis in the heart.

Acute myotoxic and nephrotoxic effects of Aipysurus laevis venom following intramuscular injection in mice.

We studied the local toxic effects on muscle and kidney following injections of incremental doses of crude Aipysurus laevis venom in mice. Mice were sacrificed at 24 hours after intramuscular injection. The soleus muscle and kidneys were examined by light microscopy. Injected muscle showed coagulative necrosis and inflammation, the severity of the damage increased with increasing dose of toxin injected, reaching a peak at a dose of 0.2 mg/kg body weight. Our findings suggest that the venom is directly myotoxic, mainly affecting mitochondrial rich fibres. The associated inflammatory response is probably secondary to muscle damage rather than a direct toxic effect of the venom. There is also renal damage which is more severe than that seen following subcutaneous venom injection in our previous studies. This can be explained by a more rapid absorption of injected venom.