ABSTRACT
Abstract The prolonged entry of large amounts of calcium into the mitochondria through the mitochondrial calcium uniporter complex (MCUC) may cause the permeability transition pore (mPTP) to open, which contributes to the pathogenesis of several diseases. Tissue-specific differences in mPTP opening due to variable expression of MCUC components may contribute to disease outcomes. We designed this study to determine differential mPTP opening in mitochondria isolated from different regions of mouse brain and kidney and to compare it with the expression of MCUC components. mPTP opening was measured using mitochondria isolated from the left/right brain hemispheres (LH/RH, respectively) and from kidney cortex/medulla, while the expression level of MCUC components was assessed from total cellular RNA. Interestingly, LH mitochondria showed less calcium-induced mPTP opening as compared to RH mitochondria at two different calcium concentrations. Conversely, mPTP opening was similar in the renal cortex and renal medulla mitochondria. However, the kidney mitochondria demonstrated bigger and faster mPTP opening as compared to the brain mitochondria. Furthermore, asymmetric mPTP opening in the LH and RH mitochondria was not associated with the expression of MCUC components. In brief, this study demonstrates thus far unreported asymmetric mPTP opening in mouse brain hemispheres that is not associated with the mRNA levels of MCUC components.
Subject(s)
Animals , Male , Female , Mice , Brain , Calcium/agonists , Cerebrum/abnormalities , Mitochondrial Permeability Transition Pore/analysis , Mice , Mitochondria , 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine/adverse effects , Kidney CortexABSTRACT
Objective To identify the optimal mono-energetic enhanced spectral CT for renal cortex in cortical phase based on the iodine concentration. Methods Fifty patients with normal renal function received the abdominal enhanced spectral CT examination.The iodine concentration and CT values of the multiple mono-energetic spectral images were measured on renal cortex in cortical phase,and the correlation between the iodine concentration and the CT values and the coefficient of variation(CV)were analyzed. Results The correlation analysis demonstrated that the correlation coefficient was 0.994,0.994,0.993,0.987,0.976,0.960,and 0.938 between mono-energetic spectral CT images(40-100 keV with interval 10 keV,respectively)and iodine concentration(all
Subject(s)
Humans , Contrast Media , Iodine , Kidney Cortex/diagnostic imaging , Radiographic Image Interpretation, Computer-Assisted , Tomography, X-Ray ComputedABSTRACT
Abstract Purpose: To investigate the glomerular number after different warm ischemia times. Methods: Thirty two pigs were assigned into four groups. Three groups (G10, G20, and G30) were treated with 10, 20, and 30 minutes of left renal warm ischemia. The sham group underwent the same surgery without renal ischemia. The animals were euthanized after 3 weeks, and the kidneys were collected. Right kidneys were used as controls. The kidney weight, volume, cortical-medullar ratio, glomerular volumetric density, volume-weighted mean glomerular volume, and the total number of glomeruli per kidney were obtained. Serum creatinine levels were assessed pre and postoperatively. Results: Serum creatinine levels did not differ among the groups. All parameters were similar for the sham, G10, and G20 groups upon comparison of the right and left organs. The G30 group pigs' left kidneys had lower weight, volume, and cortical-medullar ratio and 24.6% less glomeruli compared to the right kidney. A negative correlation was found between warm ischemia time and glomerular number. Conclusions: About one quarter of glomeruli was lost after 30 minutes of renal warm ischemia. No glomeruli loss was detected before 20 minutes of warm ischemia. However, progressive glomerular loss was associated with increasing warm ischemia time.
Subject(s)
Animals , Male , Warm Ischemia/adverse effects , Kidney/blood supply , Kidney Cortex/blood supply , Kidney Glomerulus/blood supply , Time Factors , Random Allocation , Creatinine/blood , Models, Animal , Sus scrofa , Kidney/surgery , Kidney/physiopathology , Kidney Cortex/physiopathology , Kidney Glomerulus/surgery , Kidney Glomerulus/physiopathologyABSTRACT
Background and Aim: Due to the effects of herbs in the prevention of kidney stones, the present study aimed at assessing the effect of aqueous eryngium campestre on the prevention of pathologic alterations caused by calcium oxalate crystals induced by ethylene glycol in the cortex and medulla of rats'kidneys
Materials and Methods: To conduct the study 40 male Wistar rats, weighing 200 - 250 gr were randomly divided into 5 equal groups; i.e. the healthy control group that just received water, the negative control group receiving water with 1% ethylene glycol, the prevention groups, which in addition to 1% ethylene glycol in water were daily gavaged with 100 mg/kg, 200mg/kg, and 400 mg/kg of the plant extract. After 30 days all rats were killed and slides from each one's kidneys were prepared. The slides were stained applying H/E method and the number of their calcium oxalate crystals was checked
Results: It was found that there was a significant difference between the number of their calcium oxalate crystals in the control health and negative groups [P<0.05]. But, in the prevention group gavaged 100 mg/kg there was no significant difference with the negative group, [P>0.05]. However, in the 200mg/kg prevention group compared to the negative control one there was a significant difference in reducing the number of the crystals [P<0.05]. But in 400mg/kg the prevention group there was no significant difference with the negative control group [P>0.05]
Conclusion: It was discovered that aqueous extract of eryngium campestre is effective in preventing the accumulation of calcium oxalate crystals in the kidney
Subject(s)
Animals, Laboratory , Calcium Oxalate , Rats, Wistar , Ethylene Glycol , Kidney , Kidney Cortex , Kidney Medulla , Plant Extracts , Phytotherapy , Plants, Medicinal , Kidney Calculi/therapyABSTRACT
BACKGROUND/OBJECTIVES: Although Korean fermented foods contain large amounts of salt, which is known to exacerbate health problems, these foods still have beneficial effects such as anti-hypertension, anti-cancer, and anti-colitis properties. We hypothesized that ganjang may have different effects on blood pressure compared to same concentrations of salt. MATERIALS/METHODS: Sprague-Dawley rats were divided into control (CT), NaCl (NC), and ganjang (GJ) groups and orally administered with 8% NaCl concentration for 9 weeks. The systolic blood pressure (SBP), serum chemistry, Na⁺ and K⁺ concentrations and renal gene expressions were measured. RESULTS: The SBP was significantly increased in the NC group compared to the GJ and CT groups. In addition, the Na+ concentration in urine was higher in the GJ and NC groups than the CT group, but the urine volume was increased in the GJ group compared to the other groups. The serum renin levels were decreased in the GJ group compared to the CT group, while the serum aldosterone level was decreased in the GJ group relative to the NC group. The mRNA expression of the renin, angiotensin II type I receptor, and mineralocorticoid receptor were significantly lower in the GJ group compared to other groups. Furthermore, GJ group showed the lowest levels of genes for Na⁺ transporter in kidney cortex such as Na⁺/K⁺ ATPaseα1 (NKAα1), Na⁺/H⁺ exchanger 3 (NHE3), Na⁺/HCO₃⁻ co-exchanger (NBC), and carbonic anhydrases II (CAII). CONCLUSIONS: The decreased SBP in the GJ could be due to decreased renin and aldosterone levels in serum and increased urinary volume and excretion of Na⁺ with its transporter gene alteration. Therefore, ganjang may have antihypertensive effect despite its high contents of salt.
Subject(s)
Aldosterone , Angiotensin II , Blood Pressure , Carbonic Anhydrases , Chemistry , Gene Expression , Hypertension , Kidney Cortex , Rats, Sprague-Dawley , Receptors, Mineralocorticoid , Renin , Renin-Angiotensin System , RNA, MessengerABSTRACT
With aging the kidney exhibits progressive deterioration, with a decrease in renal function. Most of the filtered Na+ is actively reabsorbed in the proximal tubules through different transporters located in apical membrane. This process is possible because basolateral Na+/K+-ATP-ase generates electrochemical conditions necessary for energetically favorable Na+ transport. The α-subunit is the catalytic domain of Na+/K+-ATP-ase. There are three isoforms of the α/subunit present in rat kidney. The present study was undertaken to examine the expression pattern of rat α-Na+/K+-ATP-ase during senescence. We tested the impact of aging on mRNA expression of α-Na+/K+-ATP-ase in cortex and medulla of aged Wistar rats. We observed a significant expression decrease in mRNA levels and a possible change of isoform in the cortex of aged animals. These expression changes observed for αsubunit could be contributing to affect the renal function in conditions of water and salt stress.
Con el avance de la edad los riñones exhiben un deterioro funcional progresivo con disminución de la función renal. La mayor parte del sodio (Na+) filtrado es reabsorbido activamente en los túbulos proximales a través de diferentes transportadores ubicados en la membrana apical. Este proceso es posible por la existencia de la Na+/K+-ATP-asa basolateral, que genera las condiciones electroquímicas necesarias para que el transporte de Na+ sea energéticamente favorable. La subunidad αde la Na+/K+-ATP-asa es el dominio catalítico de la enzima. Existen tres isoformas de subunidad α, que están presentes en el riñón de la rata. En este trabajo se examinan los patrones de expresión de la α-Na+/K+-ATP-asa durante la senescencia. Se estudió así si el aumento de la edad incidía en la expresión del ARNm de la α-Na+/K+-ATP-asa en corteza y médula renal de ratas Wistar senescentes. Se observó una disminución en la expresión del ARNm de la subunidad αy un posible cambio de isoforma predominante en la corteza de los animales senescentes. Los cambios observados para la expresión de la subunidad αpodrían contribuir a afectar la función renal en condiciones de estrés hídrico y salino.
Subject(s)
Animals , Rats , Aging/metabolism , RNA, Messenger/metabolism , Sodium-Potassium-Exchanging ATPase/metabolism , Kidney Cortex/enzymology , Kidney Medulla/enzymology , Sodium/metabolism , RNA, Messenger/analysis , Base Sequence , Random Allocation , Rats, Wistar , Sodium-Potassium-Exchanging ATPase/analysis , Sodium-Potassium-Exchanging ATPase/geneticsABSTRACT
Introduction: Lithium is a therapeutic agent currently used for the treatment of aff ective disorders controlling a variety of neurotic and psychosomatic manic depressions. Th e main objective of the present work was to demonstrate the histopathological eff ects of the therapeutic doses of Lithium on the renal tubules and glomeruli in growing albino rats. Material and Methods: Th irty growing male Sprague – Dawley albino rats were used in this study. Th e rats were divided into a control group formed of 6 rats and an experimental group formed of 24 rats which received a daily therapeutic dose of 20 mg Lithium/kg body weight by the same route for 7 weeks. Th e renal cortex in all animals is examined by light and electron microscopes. Blood was collected from the sacrifi ced animals for serum creatinine, urea, sodium and potassium to access the eff ect of lithium administration in a therapeutic dose on renal function. Results: Th e present work revealed that the therapeutic doses of Lithium induced nephrotoxicity in the form of degeneration and necrosis in the renal tubules and glomeruli. Alteration in the cellular fi ne structure and degenerated cytoplasm and cytoplasmic organelles were found revealing cellular degeneration and necrosis. Glomerulosclerosis and congestion were the predominant eff ect on the renal glomeruli. Conclusion: Histological and ultrastructrual features of Lithium nephrotoxicity were detected in the current study with therapeutic doses of Lithium.
Subject(s)
Albinism , Animals , Kidney Cortex/analysis , Kidney Cortex/anatomy & histology , Kidney Cortex/drug effects , Kidney Cortex/physiology , Kidney Cortex/ultrastructure , Lithium/adverse effects , Lithium/toxicity , Rats, WistarABSTRACT
<p><b>OBJECTIVE</b>To observe the effect of Cordyceps sinensis (CS) powder on renal oxidative stress and mitochondria functions in 5/6 nephrectomized rats, and to primarily explore its possible mechanisms.</p><p><b>METHODS</b>Totally 30 male Sprague-Dawley rats were divided into the sham-operation group, the model group, and the treatment group by random digit table, 10 in each group. A chronic kidney disease (CKD) rat model was prepared by one step 5/6 nephrectomy. Rats in the treatment group were intragastrically administered with CS powder solution at the daily dose of 2 g/kg, once per day. Equal volume of double distilled water was intragastrically administered to rats in the sham-operation group and the model group. All medication lasted for 12 weeks. The general condition of rats, their body weight, blood pressure, 24 h proteinuria, urinary N-acetyl-β-D-glucosaminidase (NAG), serum creatinine (SCr) , and blood urea nitrogen (BUN) were assessed before surgery, at week 2, 4, 6, 8, 10, and 10 after surgery. Pathological changes of renal tissues were observed under light microscope. Morphological changes of mitochondria in renal tubular epithelial cells were observed under transmission electron microscope. Activities of antioxidant enzymes including reduced glutathione (GSH), manganese superoxide dismutase (MnSOD), and malondialdehyde (MDA) in fresh renal tissue homogenate were detected. Mitochondria of renal tissues were extracted to detect levels of mitochondrial membrane potential and changes of reactive oxygen species (ROS). And expressions of cytochrome-C (Cyto-C) and prohibitin in both mitochondria and cytoplasm of the renal cortex were also measured by Western blot.</p><p><b>RESULTS</b>(1) Compared with the sham-operation group, body weight was significantly decreased at week 2 (P <0. 01), but blood pressure increased at week 4 (P <0. 05) in the model group. Compared with the model group, body weight was significantly increased at week 12 (P <0. 01), but blood pressure decreased at week 8 (P < 0. 01) in the treatment group. (2) Compared with the sham-operation group, 24 h proteinuria, urinary NAG, blood SCr and BUN significantly increased in the model group (all P <0. 01). Compared with the model group, blood and urinary biochemical indices all significantly decreased in the treatment group (all P <0. 01). (3) Results of pathological renal scoring: Glomerular sclerosis index, scoring for tubulointerstitial fibrosis, degree of tubulointerstitial inflammatory infiltration were all obviously higher in the model group than in the sham-operation group (all P <0. 01). All the aforesaid indices were more obviously improved in the treatment group than in the model group (all P <0. 01). (4) Compared with the sham-operation group, activities of MnSOD and GSH-Px were significantly reduced, but MDA contents obviously increased in the renal cortex of the model group (all P <0. 01). Compared with the model group, activities of MnSOD and GSH-Px obviously increased (P <0. 05, P <0. 01), but MDA contents obviously decreased in the renal cortex of the treatment group (P <0. 01). (5) Compared with the sham-operation group, the mitochondrial membrane potential significantly decreased, but ROS levels significantly increased in the model group (all P <0.01). Compared with the model group, mitochondrial transmembrane potential increased in the treatment group, thereby inhibiting the tendency of increased production of ROS (both P < 0. 01). (6) Results of Western blot showed that, compared with the sham-operation group, expression levels of mitochondrial Cyto-C and Prohibitin were significantly reduced in the renal cortex (P <0. 01), but significantly elevated in the cytoplasm of the model group (P <0. 01). Compared with the model group, each index was obviously improved in the treatment group with statistical difference (P <0. 05, P <0. 01).</p><p><b>CONCLUSION</b>CS powder had renal protection, and its mechanism might partially depend on in- hibition of oxidative stress and protection for mitochondria.</p>
Subject(s)
Animals , Male , Rats , Acetylglucosaminidase , Metabolism , Blood Urea Nitrogen , Cordyceps , Drugs, Chinese Herbal , Pharmacology , Kidney , Kidney Cortex , Kidney Diseases , Kidney Function Tests , Malondialdehyde , Metabolism , Mitochondria , Nephrectomy , Oxidative Stress , Proteinuria , Rats, Sprague-Dawley , Superoxide Dismutase , MetabolismABSTRACT
PURPOSE: To evaluate changes in differential renal function (DRF), as a functional outcome, in children who underwent redo pyeloplasty for management of failed pyeloplasty and to examine the factors that affect functional outcomes. MATERIALS AND METHODS: Between January 2002 and November 2010, a total of 18 patients who underwent redo pyeloplasty for persistent ureteropelvic junction obstruction after failed pyeloplasty were enrolled in this study. We assessed perioperative factors and evaluated changes in renal cortical thickness (RCT), renal function, and hydronephrosis by use of serial ultrasound and diuretic renography. RESULTS: The mean follow-up period was 44.83+/-28.86 months. After redo pyeloplasty, prevention of further functional deterioration was observed in only 12 of the 18 patients. After dividing the patients according to this observation, we discovered significant differences in both change in DRF (dDRF) and change in RCT (dRCT) (difference between before and after initial pyeloplasty) between the two groups (p<0.001). Additionally, we noted a significant positive correlation between dRCT and dDRF. All patients showed improvements in hydronephrosis grade and relief of symptoms compared with before redo pyeloplasty. CONCLUSIONS: Redo pyeloplasty should be considered in cases of failed pyeloplasty to preserve renal function and obtain relief from symptoms. If patients show severe deterioration of DRF or a decrease in RCT after initial pyeloplasty, preservation of DRF in these patients after redo pyeloplasty could be difficult. Therefore, redo pyeloplasty should be performed before severe deterioration of DRF or decrease in RCT.
Subject(s)
Adolescent , Child , Child, Preschool , Female , Humans , Infant , Male , Disease Progression , Follow-Up Studies , Hydronephrosis/etiology , Kidney/physiopathology , Kidney Cortex/pathology , Kidney Function Tests/methods , Kidney Pelvis/surgery , Postoperative Period , Prognosis , Reoperation/adverse effects , Retrospective Studies , Treatment Failure , Treatment Outcome , Ureteral Obstruction/complications , Ureteral Obstruction/surgeryABSTRACT
PURPOSE: Because the shock wave passes through various body tissues before reaching the stone, stone composition may affect the treatment efficacy of shock wave lithotripsy (SWL). We investigated the effect of various tissue components along the shock wave path on the success of SWL. MATERIALS AND METHODS: From October 2008 to August 2010, a total of 206 patients with kidney stones sized 5 to 20 mm were prospectively recruited for a study of the factors that affect the outcome of treatment with a Sonolith Vision lithotripter. Successful SWL was defined as either stone-free status or residual fragments <4 mm at 12 weeks. Logistic regression analysis was performed to assess the factors that predicted treatment outcomes. Potential predictors included the patient's age, shock wave delivery rate, stone volume (SV), mean stone density (MSD), skin-to-stone distance (SSD), and the mean thickness of the three main components along the shock wave path: renal cortical thickness (KT), muscle thickness (MT), and soft-tissue thickness (ST). RESULTS: The mean age of the patients was 53.8 years (range, 25-82 years). The overall treatment success rate after one session of SWL was 43.2%. The mean KT, MT, and ST were 26.9, 16.6, and 40.8 mm, respectively. The logistic regression results showed that a slower shock wave delivery rate, smaller SV, a lower MSD, and a thicker KT were found to be significant predictors for successful SWL. SSD, MT, and ST were not predictors of successful treatment. CONCLUSIONS: Among the main tissue components along the shock wave path, a thicker KT was a favorable factor for successful SWL after adjustment for SV, MSD, and the shock wave delivery rate.
Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Kidney Calculi/therapy , Kidney Cortex/diagnostic imaging , Lithotripsy , Logistic Models , Prospective Studies , Tomography, X-Ray Computed , Treatment OutcomeABSTRACT
La muerte celular programada y la fibrosis renal son procesos inherentes a la enfermedad renal crónica y, en tal sentido, ha sido recientemente descripta una clara desregulación de la maquinaria respiratoria mitocondrial en pacientes con enfermedad renal crónica asociada con un aumento del estrés oxidativo. Las células tubulares lesionadas vinculadas a los macrófagos intersticiales y miofibroblastos producen citoquinas y factores de crecimiento que promueven un estado inflamatorio, inducen la apoptosis de las células tubulares y facilitan la acumulación de matriz extracelular. La angiotensina II desempeña un papel central en la fibrogénesis renal y conduce a una rápida progresión de la enfermedad renal crónica. Los niveles crecientes de la angiotensina II inducen citoquinas pro-inflamatorias, la activación de NF-kB, moléculas de adhesión, quimiocinas, factores de crecimiento y estrés oxidativo. Toda la evidencia actual sugiere que la angiotensina II aumenta el estrés oxidativo mitocondrial, regula la inducción de apoptosis y condiciona al estado inflamatorio. Por lo tanto, existiría un papel determinante de las mitocondrias y el estrés oxidativo en el proceso inflamatorio renal. Finalmente, esta revisión resume nuestro actual conocimiento acerca de los posibles mecanismos que contribuirían con la apoptosis modulada por la inflamación y/o el estrés oxidativo durante la enfermedad renal crónica. Además, se propone un nuevo concepto de herramientas anti-inflamatorias que regulan el estrés oxidativo mitocondrial lo cual afectaría directamente al proceso inflamatorio y la apoptosis. Esta idea podría tener consecuencias atractivas sobre el tratamiento de patologías inflamatorias renales y de otras afines.
The apoptosis and renal fibrosis are processes inherent to the chronic kidney disease, and consequently a clear deregulation of the mitochondrial respiratory mechanism has been described in patients with chronic renal disease associated to an increase of the oxidative stress. The injured tubular cells linked to the interstitial macrophages and myofibroblasts produce cytokines and growth factors that encourage an inflammatory condition, inducing the apoptosis of the tubular cells and enabling the accumulation of the extracellular matrix. The angiotensin II has a central role in the renal fibrogenesis leading to a rapid progression of the chronic kidney disease. The growing levels of the angiotensin II induce pro-inflammatory cytokines, the activation of NF-kB, adhesion molecules,chemokines, growth factors, and oxidative stress. The current evidence suggests that the angiotensin II increases the mitochondrial oxidative stress, regulates the induction of the apoptosis and conditions the inflammatory process. Therefore the mitochondria and the oxidative stress would play a determinant role in the renal inflammatory process. Finally, this review summarizes our present knowledge regarding the possible mechanisms that would contribute to the apoptosis conditioned by inflammation and/or oxidative stress during the chronic renal disease. Additionally, a new concept of the anti-inflammatory tools is proposed to regulate the mitochondrial oxidative stress that would directly affect the inflammatory process and apoptosis. This concept could have positive consequences on the treatment of renal inflammatory pathologies and related diseases.
Subject(s)
Animals , Humans , Apoptosis/physiology , Mitochondria/metabolism , Mitochondria/pathology , Nephritis/etiology , Oxidative Stress/physiology , Renal Insufficiency, Chronic/etiology , Angiotensin II/metabolism , Cytoprotection , Ergocalciferols/pharmacology , Kidney Cortex/drug effects , Kidney Cortex/pathology , Kidney Tubules/drug effects , Kidney Tubules/pathology , NF-kappa B/metabolism , Nephritis/metabolism , Renal Insufficiency, Chronic/metabolism , Renal Insufficiency, Chronic/pathology , Vitamins/pharmacologyABSTRACT
Chronic exposure to malathion is still a major medical problem in occupational and environmental settings. The raised issue of the antioxidants effect on different tissues provides a new line of protection against the inevitable exposure to insecticide residues in food or through environmental contamination. The aim of the study was to determine the effects of vitamin C supplementation on renal cortical tissue after chronic exposure to malathion. Thirty female albino rats aged 3 months were divided into three equal groups: group I control adults were fed the basal diet; group II was given commercial malathion dissolved in distilled water orally by intragastric tube at a dose of 100 mg/kg/day for 2 months; and group III was given malathion in the previously described way at the same dose in addition to vitamin C [pure ascorbic acid powder] dissolved in distilled water and given orally by intragastric tube at a dose of 20 mg/100 g/day for 2 months. The specimens were obtained from the kidney and prepared for light and electron microscopic examinations. Morphometric and statistical studies were carried out in the three studied groups. It was observed that treatment with malathion disrupted the normal histological structure of the renal cortex. Thickened glomerular basement membrane was evident. There was widespread vacuolation of tubular lining epithelium and increased heterochromatin clumps in most of the nuclei. The mitochondria appeared disorganized with loss of cristae. The diameter of renal corpuscles and renal tubules increased, whereas tubular epithelium height decreased significantly compared with the control. Moderate improvement in the previous findings was detected on concomitant supplementation of vitamin C. Vitamin C supplementation played a protective role on the renal cortex exposed to chronic malathion toxicity at the subcellular level
Subject(s)
Female , Animals, Laboratory , Protective Agents , Kidney Cortex/ultrastructure , Malathion/toxicity , Microscopy, Polarization/statistics & numerical data , Microscopy, Electron, Transmission/statistics & numerical data , RatsABSTRACT
To assess the normal sonographic values of renal length and cortical thickness in healthy adults and establish reference ranges in our population for comparison when examining renal disease. Sonographic assessment of renal length and cortical thickness were performed from January 2006 to December 2011 in 252 healthy individuals who were self-referred to the El-Reshaid Renal Clinic in Kuwait. They were screened for the absence of renal abnormalities. Weight and height were measured, and body mass index [BMI] and body surface area calculated. Patients were divided into 5 age groups: 18-30, 31-40, 41-50, 51-60 and 61 -80 years, in order to generate reference graphs for renal length and cortical thickness. The mean renal lengths for the right and left kidney were 10.68 +/- 1.4 and 10.71 +/- 1.0 cm, respectively [p = 0.56] without a significant change with age. The minimum cortical thickness was 0.6 cm. The renal length correlated with the weight of the patients [p < 0.01] and their BMI [p < 0.01] but not with their height. There was no difference in renal size or cortical thickness in patients older than 60 years despite an age-related decline in the glomerular filtration rate [p < 0.001]. Renal length and cortical thickness did not vary significantly with age. Renal length correlated well with weight and BMI but not with height. Hence, establishing normal ranges of renal parameters is essential for comparison in situations where possible renal disease is being investigated
Subject(s)
Humans , Male , Female , Ultrasonography , Adult , Kidney CortexABSTRACT
<p><b>OBJECTIVE</b>To observe the effect of Chinese herbs for stasis removing and collaterals dredging (CHSRCD) upon angiotensin-converting enzyme 2-angiotensin-(1-7)-Mas axis in the renal cortex of diabetic nephropathy rats.</p><p><b>METHODS</b>Totally 89 male Sprague-Dawley rats were randomly divided into the blank control group (C group, n=22), the high-glucose high-fat control group (H group, n=10), and the streptozotocin (STZ)-injecting group (n=57). The diabetes rat model (n=50) was induced by feeding high-glucose high-fat diet in combination with intraperitoneal injection of STZ, which were further divided into the model group (M group, n=24), the irbesartan group (I group, n=13), and the CHSRCD (Z group, n=13). Rats in I and Z groups were intragastrically fed with suspension of irbesartan and CHSRCD, once daily for 16 weeks. Equal volume of drinking water was administrated to rats in the rest groups. Blood glucose and 24 h urine protein quantitation were tested at four time points. And the mRNA expression of ACE2 and Mas at various time points was detected by Real-time PCR, immunohistochemical assay, and Western blot. Quantitative analyses of ACE2 and Mas protein expression were performed at the end of week 16.</p><p><b>RESULTS</b>Compared with the C group, blood glucose increased in the H and M groups (P < 0.01). It was higher in the H group (P < 0. 01). 24 h urine protein quantitation at different time points increased in the M group, and it was higher than that in the H group (P < 0.05). Compared with the M group, 24 h urine protein quantitation decreased at the end of week 8 in the I group, and at the end of week 8 and 16 in the Z group (P < 0.05). It was lower in the Z group than in the I group at the end of week 16 (P < 0.05). Compared with the C and H groups, the expression of ACE2 mRNA in the renal cortex was lower in the M group at the end of week 16 (P < 0.01). Compared with the M group, it was higher in the Z group (P < 0. 01). There was no statistical difference in the expressions of Mas mRNA at the end of week 16 between the C group and the M group (P > 0.05). It was lower in the M group than in the H group (P < 0.05). It was higher in the Z group than in the M group (P < 0.05), and higher than in the I group (P < 0.05). The expression of ACE2 and Mas protein in the M group decreased as time went by. The expression quantitation of ACE2 and Mas protein at the end of week 16 was lower in the M group than in the C group (P < 0.05). Compared with the M group, ACE2 expression of the Z group and Mas of the I and Z groups increased more significantly (P < 0. 05).</p><p><b>CONCLUSION</b>CHSRCD could play a role in renal protection for diabetic nephropathy rats by up-regulating the mRNA and protein expression of ACE2 and Mas, promoting the ACE2-Ang-(1-7)-Mas axis, and lowering urinary protein.</p>
Subject(s)
Animals , Male , Rats , Angiotensin I , Metabolism , Diabetes Mellitus, Experimental , Metabolism , Diabetic Nephropathies , Metabolism , Drugs, Chinese Herbal , Pharmacology , Kidney Cortex , Metabolism , Peptide Fragments , Metabolism , Peptidyl-Dipeptidase A , Metabolism , Proto-Oncogene Proteins , Metabolism , Rats, Sprague-Dawley , Receptors, G-Protein-Coupled , MetabolismABSTRACT
Este estudo caracteriza a radiodensidade do córtex renal de 10 cães e 10 gatos adultos, clinicamente saudáveis, por meio de exames de tomografia computadorizada helicoidal. Em cada rim, a radiodensidade renal foi estimada pelo valor médio das três regiões de interesse na região cortical, selecionados no polo cranial, polo caudal e hilo renal. A radiodensidade média do córtex renal nos cães e nos gatos foi, respectivamente, 28,4±4,7 e 22,4±3,6 unidades Hounsfield (HU). Verificou-se que os gatos possuem córtex renal hipoatenuante quando comparado com cães, um fato que está associado à maior deposição de conteúdo lipídico nos rins felinos. A diferença na radiodensidade encontrada entre o córtex renal de cães e de gatos é importante para uma correta interpretação dos achados renais no exame tomográfico.
Subject(s)
Animals , Dogs/physiology , Kidney Cortex/anatomy & histology , Cats/physiology , Kidney/anatomy & histology , Tomography/methodsABSTRACT
Paracetamol or acetaminophen [IV-acetyl-p-aminophenol; APAP] is a widely used analgesic and antipyretic drug. Unfortunately, it is now reported as the most common cause of toxic ingestion in the world. Nigella sativa oil [NSO] is an extract of N. sativa having antioxidant properties. This study aimed to assess the possible role of NSO in ameliorating the toxic effect of APAP overdose on the rat renal cortical structure. Thirty male albino rats were divided into three equal groups. Group I was the control group. Group II comprised rats treated with APAP [750 mg/kg/day] orally for 7 days. Group III received NSO [2 ml/kg/day orally] 30 min before oral administration of APAP at the same dose as that of group II for 7 days. Kidney specimens were processed for light and electron microscopic study of the renal cortex. Plasma renin activity and arterial blood pressure were estimated. APAP-treated rats showed marked structural changes in the proximal convoluted tubules with dense nuclear staining, cytoplasmic vacuolization, increased peroxisomes, and partial loss of apical brush border and basal striations. Renal corpuscles revealed focal fusion of podocyte foot processes and irregular thickening of glomerular basement membranes. Juxtaglomerular cells contained few renin granules, reflecting an increase in renin exocytosis that coincided with increased plasma renin activity and increased arterial blood pressure. Concomitant administration of NSO with APAP revealed a noticeable amelioration of these histological and physiological changes. NSO exerted a protective effect against APAP-induced renal cortical damage
Subject(s)
Animals, Laboratory , Kidney Cortex/pathology , Kidney Cortex/ultrastructure , Microscopy, Electron , Protective Agents , Nigella sativa/drug effects , Plant Oils , RatsABSTRACT
Carbon tetrachloride [CCl[4]] has long been known as a model toxicant. Antioxidants are used to antagonize the deleterious action of free radicals. Numerous reports suggest that both curcumin and ginger have antioxidant effects. This work was carried out to compare between the possible protective roles of curcumin and ginger on renal corpuscles of CCl[4]-treated adult male albino mice using light and electron microscopes. A total of 45 adult male albino mice were used for this study and were divided into four groups: group I served as the control group. Group II received 0.2 ml/kg CCl[4] subcutaneously twice a week for 4 weeks. Group III received CCl[4] and curcumin concomitantly at a dose of 80 mg/kg once daily orally for 4 weeks. Group IV received CCl[4] and 1 ml of ginger at a dose of 24 mg/ml once daily orally for 4 weeks. At the end of the experiment, renal specimens were processed for light and electron microscopic study. Morphometric analysis was also carried out on electromicrographs to evaluate for filtration barrier integrity. Renal corpuscles of CCl[4]-treated mice showed shrunken, lobulated, and hypercellular glomeruli with podocytic affection and mesangial cell proliferation. Morphometric analysis displayed disruption of filtration barrier integrity. Both curcumin and ginger resolved most of these morphological alterations. However, ginger was proven to be more potent than curcumin. Concomitant administration of ginger with CCl[4] has a more protective effect than curcumin on the renal corpuscles of adult male albino mice
Subject(s)
Male , Animals, Laboratory , Kidney Cortex/ultrastructure , Microscopy, Electron , Protective Agents , Zingiber officinale/drug effects , Curcumin , Comparative Study , MiceABSTRACT
Hepatic ischemia/reperfusion [I/R] injury is an unavoidable problem during liver surgery that often results in acute liver failure, with its complications. Losartan may be beneficial in such conditions. This study was designed to investigate the histological and biochemical alterations that could occur in the renal cortex in case of liver cell failure and to assess the possible protective role of losartan. Thirty male albino rats were equally divided into three groups: group I [control] was equally subdivided into sham operated-untreated [Ca] and sham-operated, losartan-treated [Cb] subgroups. In group II [operated], rats were subjected to experimentally induced I/R. In group III [losartan treated], rats were subjected to a surgical procedure and treated with losartan [5 mg/kg body weight]. At the end of the experiment, blood samples were obtained for the biochemical assay. The liver was processed for assessment of antioxidant markers and for light microscope examination. Both kidneys were processed for light and electron microscope examinations. The results were morphometrically and statistically analyzed. Light microscope examination of the operated group indicated shrunken glomeruli with wide Bowman's space. Some tubules were distorted with cytoplasmic vacuoles and cellular casts, whereas others were dilated. The interstitium contained an acidophilic material, increased collagen fibers, cellular infiltration, and congested blood vessels. Ultrastructurally, podocytes had small electron-dense nuclei and fused foot processes. Some renal tubules had small heterochromatic nuclei, mitochondria with disrupted cristae, and small electron-dense bodies. The biochemical results of the same group showed the occurrence of oxidative stress and deterioration in liver and kidney functions. The treated group showed preserved structure of the renal corpuscles and tubules. Liver I/R adversely affected the renal cortex histologically and biochemically. Losartan could be promising as an adjuvant therapy before hepatic surgery for rescuing the kidney from hepatic I/R injury
Subject(s)
Animals, Laboratory , Liver Failure/complications , Kidney Cortex/pathology , Kidney Cortex/ultrastructure , Microscopy, Electron , Protective Agents , Losartan , Treatment Outcome , RatsABSTRACT
Exposure to titanium dioxide nanoparticles [TiO[2] NPs] results from its wide use in the fields of medicine, industry, engineering, and environmental technology. To investigate the effect of administration of TiO[2] NPs on the ultrastructure of the rat liver and renal cortex. Rats were subdivided into two groups: group A [served as control] and group B [TiO[2] group]. TiO[2] was suspended in PBS and administered by an oral gavage to the rats of group B daily for 90 days at a dose of 5 mg/kg body weight. Thereafter, group B was subdivided into group B1 and sacrificed 24 h after the last dose of titanium. Group B2 was left untreated for 12 months and then sacrificed. Specimens from the liver and renal cortex were obtained and processed for examination by transmission electron microscopy. Histopathological changes were detected in the hepatocytes of group B1 in the form of dilated rough endoplasmic reticulum, numerous lysosomes, and abnormal mitochondria. Moreover, accumulation of large lipid droplets and wide cytoplasmic vacuoles was observed. The renal cortex was also affected. Numerous lysosomes were observed in the lining cells of the proximal tubules and the glomerulus showed an apparent increase in the number of mesangial cells. The interstitium was the site of excessive collagen bundles. These hepatic and renal cortical changes were partially ameliorated 12 months after the last dose of TiO[2]. Small doses of TiO[2] NPs for a long duration resulted in a variety of degenerative changes in the rat liver and renal cortex. Therefore, further studies are required to investigate the underlying mechanisms of this toxicity and to search for possible protective measures
Subject(s)
Animals, Laboratory , Liver/pathology , Kidney Cortex/pathology , Liver/ultrastructure , Kidney Cortex/ultrastructure , Microscopy, Electron , Rats , Nanoparticles/adverse effectsABSTRACT
Monosodium glutamate [MSG] is a widely used flavour enhancer. Its use in high concentration could affect vital functions, including those of the kidney. The present study is concerned with evaluation of the effect of prenatal and postnatal MSG administration on the developing male albino rat renal cortex. Twenty pregnant female albino rats were divided into two equal groups: group I [control] and group II [treated]. In group II, MSG was administered orally at a dose of 2 mg/kg/day from the 12th day of gestation until the 21st day postnatally. After delivery, the offspring of both groups were sacrificed at the newborn stage, at 3 weeks and at 3 months. Kidney specimens were processed for examination by light and scanning electron microscopy. Maternal MSG administration affected both the renal glomeruli and tubules of the offspring. In the newborn stage, the glomeruli at the subcapsular zone appeared immature and crowded. The foot processes showed apparent elongation and disruption of their interdigitations. In weaned rats, apparent widening of Bowman's space in some glomeruli, detachment of podocytes and effacement of foot processes were noticed. In adult rats, the glomeruli showed hypercellularity with apparent elongation and fusion of the foot processes. The renal tubules at the different ages studied showed degenerative changes with sloughs inside the lumen of some tubules accompanied by proliferative changes. The proximal tubules showed partial loss of the brush border. MSG causes a delay in the development of glomeruli. Some glomeruli showed hypercellularity with affection of podocytes, which makes the glomeruli liable to glomerulosclerosis