Number Of Renal Glomeruli Research Articles

Morphological criteria for Pipistrellus pygmaeus kidney indicators

At present, there is scientific and practical interest in the study of morphological and physiological features, criteria and tolerance of organs involved in protein metabolism in representatives of the order Chiroptera. Macro- and micrometric indicators of kidneys in soprano pipistrelle (Pipistrellus pygmaeus), as a result of adaptive transformations of the body to habitat conditions in the Bryansk region were studied. The study was conducted in the period from 2011 to 2022, 40 captures were carried out with a total of 481 individuals, of which 100 were selected for further study. On histological preparations of kidneys of soprano pipistrelle (Pipistrellus pygmaeus), morphometry of nephrons, podocyte parameters, nuclear-cytoplasmic ratio, areas of nucleolar organizers and their total area were studied. It was established that biological adaptation of the bats (Chiroptera), on the example of soprano pipistrelle (Pipistrellus pygmaeus), is manifested in development of biological properties of the species. The functional and protein-synthetic activity of cells, kidneys (cell volume, nucleus, cytoplasm and nuclear-cytoplasmic ratio), the number and increase in the total area of the argentophilic region of nucleolar organizers were determined by organ topography, gender and influence of anthropogenic negative environmental effects. The data obtained showed gender differences in female bats (Chiroptera) of Pipistrellus pygmaeus species living in an urban environment, having a large number in the colony, against the background of a combined anthropogenic load, under the influence of hydrocarbons, sulfur and nitrogen dioxides and suspended solids. It was found that phenotypic adaptation as an adaptation to flight triggers the main processes of biochemical cycles, the processes of endogenous intoxication and detoxification function in kidneys. In turn, it increases metabolism, which contributes to increase in the number of renal glomeruli and decrease in the cavity of renal glomerular capsule. New data characterizing nuclear-cytoplasmic ratio, number and total area of regions of nucleolar organizers in podocytes of glomeruli in kidneys of soprano pipistrelle (Pipistrellus pygmaeus), which may be a manifestation of genetic adaptation to environmental conditions, were obtained.

MON-053 CLINICAL AND PATHOLOGICAL CHARACTERISTICS OF IgA NEPHROPATHY WITH AKD

IgA nephropathy is one of the most common types of primary glomerulonephritis worldwide.It was found that the creatinine of IgA nephropathy could increase in a short time even reaching the diagnostic standard of acute kidney disease（AKD）in clinical work. However, the factors for the occurrence in these patients were unclear. Here,we did a research to explore the clinical features and kidney pathological characteristics of IgA nephropathy patients with AKD and the related factors influencing its recovery. Patients between 2011 and 2016 taken from the First Affiliated Hospital of Zhengzhou University were enrolled in the study.The number of renal glomeruli in all cases was more than or equal to 10.The secondary IgA nephropathy such as systemic lupus erythematosus, purpura nephritis, chronic liver diseases was not included.The 2012 KDIGO guidelines were adopted as the criteria to screen the IgA nephropathy patients with AKD. The baseline data, clinical and renal pathological data were collected.According to the degree of the decline of estimated glomerular filtration rate(eGFR), the IgA nephropathy patients with AKD were divided into three groups with the eGFR decreased by 35-50% in group A, 51-75% in group B, and 76% or more in group C.Then according to the recovery degree of the renal function, the patients were divided into two groups with the recovery group (fully recovery of renal function or partial recovery) and the non-recovery group(no obvious change of renal function or progression of renal function).The clinical features and kidney pathological characteristics of the three groups and the related factors affecting their recoveries were analyzed. A total of 1855 patients were included of which 128 patients occurred to AKD, accounting for 6.9%.There were significant differences in calcium, phosphorus,hemoglobin,albumin,urea nitrogen and urine leukocyte in the three groups (p < 0.05).We followed up the IgA nephropathy patients with AKD for 6 months and found that the creatinine level of 26 patients was not better or even progressed compared with the peak of creatinine during hospitalization, while the creatinine level of 102 patients was lower or completely restored to the baseline.High blood pressure and large amount of proteinuria are the factors that affect the recovery of renal function of AKD.At the same time, we take these patients for a long-term follow-up with the average follow-up time to 3.8 years with the result that 35 patients entered end-stage renal disease(ESRD) or died. The degree of decreased glomerular filtration rate in IgA nephropathy patients with AKD is related to clinical and pathological characteristics and IgA nephropathy patients occurred with AKD are more likely to enter the ESRD.

Histological evaluation of kidney development in young rats after a surgery and management of wound with fibrin glue

Aim. The subject of this study is evaluation of histological hallmarks of kidney growth in rats after a surgery and subsequent management of the wound with fibrin glue. Material and Methods. Sixty-five Wistar rats underwent a surgical procedure resulting in parenchymal injury by incision followed by an application of fibrin glue. Kidneys have been examined and evaluated histologically after 4 weeks (group I) and 26 weeks (group II) after the surgery Results. When fibrin glue was used, in both groups, regular anastomoses of the wound edges of the kidney after surgery were noted. Histological features of kidney growth (renal glomeruli, renal tubules and blood vessels) were observed in the parenchyma and in the postoperative scar. In the second group kidneys grew on average by 3.5mm in the longitudinal section and by 1.89 in the cross section. In this group, the number of renal glomeruli nearly doubled. Glomeruli and tubules were also found in the postoperative scar.

Protective Effects of DX-9065a, an Orally Active, Novel Synthesized and Selective Inhibitor of Factor Xa, Against Thromboplastin-Induced Experimental Disseminated Intravascular Coagulation in Rats

We investigated the protective effects of DX-9065a, an orally active, newly synthesized, and specific inhibitor of factor Xa, against experimental disseminated intravascular coagulation (DIC) in rats. Experimental DIC was induced by a 4 hour sustained infusion of thromboplastin at a dose of 2.5 mg/kg. The rats were orally administered DX-9065a at 10, 30, 100 mg/kg 30 minutes before thromboplastin injection. In this DIC model, DX-9065a showed a protective effect against DIC, at all doses and in all parameters, including fibrin(ogen) degradation products, fibrinogen level, thrombin-antithrombin III complex level, prothrombin time (PT), activated partial thromboplastin time (APTT), platelet count, and the number of renal glomeruli with fibrin thrombi. When DX-9065a was orally administered at 100 mg/kg without thromboplastin, no significant changes were seen in hemostatic parameters except PT and APTT, and no fibrin thrombi or abnormal bleeding were seen in renal specimens. These findings suggested that the new oral anti-Xa drug, DX-9065a, has a protective effect against thromboplastin-induced DIC model with little risk of bleeding.

Effects of DX-9065a, an Orally Active, Newly Synthesized and Specific Inhibitor of Factor Xa, against Experimental Disseminated Intravascular Coagulation in Rats

We investigated the protective effects of DX-9065a, an orally active, newly synthesized and specific inhibitor of factor Xa, against two kinds of experimental disseminated intravascular coagulation (DIC) in rats. Endotoxin-induced experimental DIC was induced by a 4-h sustained infusion of endotoxin at a dose of 100 mg/kg. Thromboplastin-induced experimental DIC was induced by a bolus injection of thromboplastin at a dose of 150 mg/kg. The rats were orally administered DX-9065a at 10, 30 or 100 mg/kg 30 min before endotoxin or thromboplastin injection. In both DIC models, DX-9065a showed a protective effect against DIC, at all doses and in all parameters, including fibrin/fibrinogen degradation products (FDP), fibrinogen level, prothrombin time, activated partial thromboplastin time, platelet count and the number of renal glomeruli with fibrin thrombi. When DX-9065a was orally administrated at 100 mg/kg without endotoxin or thromboplastin, no significant changes were seen in hemostatic parameters except PT and APTT, and no fibrin thrombi or abnormal bleeding were seen in renal specimens. These findings suggest that the new oral anti-Xa drug, DX-9065a, has an effect in reducing the severity of DIC. However, further dose-finding and safety studies of this drug have still to be assessed.

Evaluation and comparison of automated biopsy devices. Work in progress.

The performance of four automated biopsy devices (Bard Biopty, Bard Monopty, Microvasive ASAP 18, Medical Device Technologies Ultra-Cut) was compared when they were used to obtain 96 liver and 96 kidney samples from eight dogs under ultrasound guidance. There was no significant difference in the lengths of the samples obtained with the four devices. The Monopty device yielded a significantly greater mean weight of both kidney (30.8%) and liver (31.6%) samples compared with the other devices. There were no significant differences between the four devices relative to cellular and histologic preservation, crush artifact, and number of renal glomeruli or liver lobules and portal triads. Renal subcapsular hematomas were identified in most instances, and there was no difference between the devices in the amount of renal trauma resulting from their use. There was only one instance of severe injury to the liver. The choice of instrument should remain one of personal preference, since all four devices were satisfactory and none produced significantly greater renal or hepatic injury.

Protective effects of ONO-3307, a new synthetic protease inhibitor against experimental disseminated intravascular coagulation in rats

The effects of ONO-3307 (4-sulfamoylphenyl 4-guanidinobenzoate methanesulfonate), a new synthetic protease inhibitor, on endotoxin-induced experimental disseminated intravascular coagulation (DIC) were studied in rats. Experimental DIC was induced by a 4-h sustained infusion of endotoxin at a dose of 100mg/kg. The rats were infused continuously with ONO-3307 at a dose of 1, 10 or 100 μg/kg/h into a femoral vein for 4 h. Simultaneously with the agent infusion, endotoxin (100mg/kg/ 4h) was administered into the contralateral femoral vein. A protective effect against DIC was noted in the rats treated with 10 or 100 μg/kg/h of ONO-3307 in the following parameters: fibrinogen and fibrin degradation products, fibrinogen level, prothrombin time, partial thromboplastin time, platelet count and the number of renal glomeruli with fibrin thrombi. Therefore, ONO-3307 inhibited the aggravation of endotoxin-induced experimental DIC in rats.

Vascular alterations in the canine kidney following obstruction of the urinary tract. A SEM investigation of corrosion casts.

Changes in the vasculature of the canine kidney following four weeks obstruction of the ureter via double ligature is described on the basis of SEM investigation. Three significant alterations were observed: 1) A two-thirds reduction in the depth of the renal cortex as compared to controls. 2) Rarification of the entire cortical capillary bed. 3) Reduction in both the number and diameter of the glomeruli. The rarification of the post-glomerular capillaries is interpreted to be a pressure atrophy, whereas the reduction in the number of renal glomeruli and the concommitant diminuation of their capillary loops is thought to represent a functional atrophy.

新しく合成されたプロテアーゼインヒビターＯＮＯ‐３３０７によるエンドトキシンＤＩＣの阻止効果

The effects of ONO-3307 (4-sulfamoylphenyl 4-guanidinobenzoate methanesulfonate), a new synthetic protease inhibitor, on endotoxin-induced experimental disseminated intravascular coagulation (DIC) were studied in rats. Experimental DIC was induced by 4 hour sustained infusion of endotoxin at a dose of 100mg/kg. The rats were infused continuously with ONO-3307 at 1, 10, 100μg/kg/h into a femoral vein for 4 hour. Simultaneously with the agent infusion, endotoxin was administered into the contralateral femoral vein. A protective effect against DIC was noted in the rats treated with 10 or 100μg/kg/h of ONO-3307 in the following parameters: fibrinogen and fibrin degradation products, platelet count, fibrinogen level, prothrombin time, partial thromboplastin time and the number of renal glomeruli with fibrin thrombi. These results demonstrated that ONO-3307 reduces the extent of changes of the coagulation parameters caused by DIC.

Endotoxin-induced disseminated intravascular coagulation in vitamin E deficient rats

The effect of vitamin E on endotoxin-induced experimental disseminated intravascular coagulation (DIC) was studied in rats deficient in and supplemented with vitamin E. Experimental DIC was induced by a 4-hr sustained infusion of endotoxin at a dose of 13.3 mg/kg. After the infusion, fibrinogen and fibrin degradation products were increased, platelet count and fibrinogen level were decreased, and prothrombin time and partial thromboplastin time were prolonged. In addition, the number of renal glomeruli with fibrin thrombi was increased. These changes were significantly greater in vitamin E deficient rats when compared to those changes found in rats supplemented with vitamin E. These results indicate that vitamin E plays a protective role in endotoxin-induced DIC.

Effect of dipyridamole on experimental disseminated intravascular coagulation in rats

Experimental disseminated intravascular coagulation (DIC) can be induced by 4-h sustained infusion of endotoxin in a dose of 100 mg/kg in rats. The experimental model of DIC in rats was used to study the preventive effect of dipyridamole against DIC. Before the infusion of endotoxin, 0.5, 5.0 or 50.0 mg/kg of dipyridamole was injected intraperitoneally. The preventive effect against DIC was noted in all the parameters, such as fibrinogen and fibrin degradation products, fibrinogen level, prothrombin time, partial thromboplastin time, platelet count, and the number of renal glomeruli with fibrin thrombi, in rats treated with 5.0 or 50.0 mg/kg of dipyridamole. From these results, it was shown that dipyridamole inhibited the aggravation of endotoxin-induced experimental DIC in rats.

Effects of Superoxide Dismutase and Catalase on Disseminated Intravascular Coagulation In Rats

The effects of superoxide dismutase (SOD) and catalase on endotoxin-induced experimental disseminated intravascular coagulation (DIC) were studied in rats. Experimental DIC was induced by a 4 hr sustained infusion of endotoxin at a dose of 100 mg/kg. The rats were subcutaneously injected with SOD at 0.5, 5.0 or 50.0 mg/kg, or catalase at 0.01, 0.1 or 1.0 mg/kg, followed by the continuously infusion of 100 mg/kg/4hr of endotoxin. A preventive effect against DIC was noted in all the parameters, such as fibrinogen and fibrin degradation products, fibrinogen level, prothrombin time, partial thromboplastin time, platelet count and the number of renal glomeruli with fibrin thrombi, in the rats treated with 50.0 mg/kg of SOD or 1.0 mg/kg of catalase. When 50.0 mg/kg of SOD or 1.0 mg/kg of catalase was injected subcutaneously at 1, 2 or 3 hr after the initiation of the endotoxin-infusion, the protective effect against DIC was noted in all the parameters.

Protective effect of gabexate mesilate against experimental disseminated intravascular coagulation in rats.

Experimental disseminated intravascular coagulation (DIC) can be induced by 4 h sustained infusion of endotoxin at a dose of 100 mg/kg in rats. The experimental model of DIC in rats was used to study the preventive effect of gabexate mesilate (GM) against DIC. Before the infusion of endotoxin, 10(-6), 10(-3), 1, 10, 50 or 100 mg/kg of GM was injected intraperitoneally. The preventive effects against DIC were noted in all the parameters, such as fibrinogen and fibrin degradation products, fibrinogen level, prothrombin time, partial thromboplastin time, platelet count, and the number of renal glomeruli with fibrin thrombi, in rats treated with 1, 10 or 50 mg/kg of GM. From these results it was shown that GM inhibited the aggravation of endotoxin-induced experimental DIC in rats.

Effects of Ticlopidine and Aspirin on Endotoxin-Induced Disseminated Intravascular Coagulation in Rats

The effects of ticlopidine and aspirin on endotoxin-induced experimental disseminated intravascular coagulation (DIC) were studied in rats. Experimental DIC was induced by a 4 hr sustained infusion of endotoxin at a dose of 100 mg/kg. The rats were intraperitoneally injected with ticlopidine at 2.0, 20.0, 50.0, 100.0 or 200.0 mg/kg, or aspirin at 0.03, 0.3, 3.0 or 30.0 mg/kg, followed by the continuous infusion of 100 mg/kg/4 hr of endotoxin. A preventive effect against DIC was noted in all the parameters, such as fibrinogen and fibrin degradation products (FDP), fibrinogen level, prothrombin time, partial thromboplastin time (PTT), platelet count and the number of renal glomeruli with fibrin thrombi, in the rats treated with 20.0, 50.0, 100.0 or 200.0 mg/kg of ticlopidine. Although a preventive effect was also noted in FDP, PTT, platelet count and the number of glomeruli with thrombi in rats treated with 0.03 or 0.3 mg/kg of aspirin, this agent was less effective than ticlopidine.

Effects of FUT-175, a new synthetic protease inhibitor on endotoxin-induced disseminated intravascular coagulation in rats.

The effects of FUT-175 (6-amidino-2-naphthyl-4-guanidino benzoate-dimethanesulfonate), a new synthetic protease inhibitor, on endotoxin-induced experimental disseminated intravascular coagulation (DIC) were studied in rats. Experimental DIC was induced by a 4-hour sustained infusion of endotoxin at a dose of 100 mg/kg. The rats were infused continuously with FUT-175 at 0.001, 0.01, 0.1, 1.0 or 10.0 mg/kg into a femoral vein for 4 h. Simultaneously with the agent infusion, endotoxin (100 mg/kg/4 h) was administered into the contralateral femoral vein. A protective effect against DIC was noted in the rats treated with 0.01 or 0.1 mg/kg of FUT-175 in the following parameters: fibrinogen and fibrin degradation products, fibrinogen level, prothrombin time, partial thromboplastin time, platelet count and the number of renal glomeruli with fibrin thrombi. These results demonstrated that FUT-175 reduces the extent of changes of the coagulation parameters caused by DIC.

Effect of Vitamin E on Endotoxin-Induced Disseminated Intravascular Coagulation in Rats

Experimental disseminated intravascular coagulation (DIC) can be induced by 4 hr sustained infusion of endotoxin in a dose of 100 mg/kg in rats. The experimental model of DIC in rats was used to study the preventive effect of vitamin E, alpha-tocopheryl acetate, against DIC. Before the infusion of endotoxin, 0.01, 0.1, 1.0 or 10.0 mg/kg/day of alpha-tocopheryl acetate was injected intraperitoneally for 4 successive days. The preventive effect against DIC was noted in all the parameters, such as fibrinogen and fibrin degradation products, fibrinogen level, prothrombin time, partial thromboplastin time, platelet count, and the number of renal glomeruli with fibrin thrombi, in rats treated with 1.0 or 10.0 mg/kg of alpha-tocopheryl acetate. From these results, it was shown that vitamin E, alpha-tocopheryl acetate, inhibited endotoxin-induced experimental DIC in rats.

Experimental model of disseminated intravascular coagulation induced by sustained infusion of endotoxin.

Experimental disseminated intravascular coagulation (DIC) was induced by sustained infusion of endotoxin into the femoral vein in rats. The severity of DIC was determined with reference to various parameters, such as fibrinogen and fibrin degradation products (FDP), prothrombin time (PT), partial thromboplastin time (PTT), platelet count, and number of renal glomeruli having fibrin thrombi. Experimental DIC could be induced by a 4-h sustained infusion of endotoxin in a dose of 100 mg/kg. The DIC induced in rats showed a close resemblance to human DIC as judged from such changes as an elevation in FDP, prolongation of PT and PTT, depression in fibrinogen and platelet count, and increase in glomeruli having fibrin thrombi. This experimental model has an advantage in that severity of DIC can be determined by measuring various parameters. It will be of use in the studies aimed at the establishment of a therapy for DIC as well as in the studies on DIC in rats.