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51.
雷涌 《南昌大学学报(理科版)》1988,12(1):1
本文报导了寄生于淡水鱼类的粘孢子虫两新种。1、井冈碘泡虫寄生于泥鳅肾脏,孢子壳面观卵形,缝面观纺锤形。2、万安单极虫寄生于玻璃红鲤鱼鳃丝,孢子壳面观椭圆形,极囊近于园形。 相似文献
52.
Sabbir Ahmed Rolf W. Sparidans Jingyi Lu Silvia M. Mihaila Karin G. F. Gerritsen Rosalinde Masereeuw 《Biomedical chromatography : BMC》2022,36(5):e5307
Proximal tubular damage is an important prognostic determinant in various chronic kidney diseases (CKDs). Currently available diagnostic methods do not allow for early disease detection and are neither efficient. Indoxyl sulfate (IS) is an endogenous metabolite and protein-bound uremic toxin that is eliminated via renal secretion, but accumulates in plasma during tubular dysfunction. Therefore, it may be suitable as a tubular function marker. To evaluate this, a fast bioanalytical method was developed and validated for IS in various species and a kidney cell line using LC–MS/MS. An isotope-labeled IS potassium salt as an internal standard and acetonitrile (ACN) as a protein precipitant were used for sample pretreatment. The analyte was separated on a Polaris 3 C18-A column by gradient elution using 0.1% formic acid in water and ACN, and detected by negative electrospray ionization in selected reaction monitoring mode. The within-day (≤ 4.0%) and between-day (≤ 4.3%) precisions and accuracies (97.7 to 107.3%) were within the acceptable range. The analyte showed sufficient stability at all conditions investigated. Finally, applying this assay, significantly higher plasma and lower urine concentrations of IS were observed in mice with diabetic nephropathy with tubular damage, which encourages validation toward its use as a biomarker. 相似文献
53.
《Biomedical chromatography : BMC》2017,31(2)
Flos Abelmoschus manihot is a traditional herbal medicine widely used in clinical practice to tackle chronic kidney disease (CKD) for thousands of years. Nowadays, many studies indicate that gut bacteria are closely related to the progression of CKD and CKD‐related complications. In this study, a UPLC‐Q‐TOF/MS method coupled with the MetaboLynx™ software was established and successfully applied to investigate the metabolites and metabolic profile of Flos A. manihot extract by intestinal bacteria from normal and CKD rats. Eight parent components and eight metabolites were characterized by their protonated ions. Among these compounds, 15 were detected in the two group samples while M16 was only determined in the CKD model samples. Compared with the quercetin‐type glycosides, fewer myricetin‐type and gossypetin‐type metabolites were obtained in the two group samples. These metabolites suggested that deglycosylation and methylation are the major metabolic pathways of Flos A. manihot extract. Few differences of metabolite classes were observed in the two group samples. However, the concentrations of aglycones such as quercetin, myricetin and gossypetin in the normal samples were notably higher than those in the CKD model samples. The results are important in unravelling the pharmacological effects of A. manihot and clarifying its mechanism of action in vivo . 相似文献
54.
Juan Eduardo Resndiz‐Galvn Melissa Romano‐Aguilar Susanna Edith Medellín‐Garibay Rosa del Carmen Miln‐Segovia Alejandro Chevaile‐Ramos Silvia Romano‐Moreno 《Biomedical chromatography : BMC》2019,33(12)
To implement and validate an analytical method by ultra‐performance liquid chromatography–tandem mass spectrometry (UPLC MS/MS) to quantify mycophenolic acid (MPA) in kidney transplant patients. Quantification of MPA was performed in an ACQUITY UPLC H Class system coupled to a Xevo TQD detector and it was extracted from plasma samples by protein precipitation. The chromatographic separation was achieved through an ACQUITY HSS C18 SB column with 0.1% formic acid and acetonitrile (60:40 vol/vol) as mobile phase. The pharmacokinetic parameters were calculated by non‐compartmental analysis of MPA plasma concentrations from 10 kidney transplant patients. The linear range for MPA quantification was 0.2–30 mg/L with a limit of detection of 0.07 mg/L; the mean extraction recovery was 99.99%. The mean intra‐ and inter‐day variability were 2.98% and 3.4% with a percentage of deviation of 8.4% and 6.6%, respectively. Mean maximal concentration of 10 mg/L at 1.5 h, area under the concentration–time curve of 36.8 mg·h/L, elimination half‐life of 3.9 h, clearance of 0.32 L/h/kg and volume of distribution of 1.65 L/kg were obtained from MPA pharmacokinetics profiles. A simple, fast and reliable UPLC–MS/MS method to quantify MPA in plasma was validated and has been applied for pharmacokinetic analysis in kidney transplant patients. 相似文献
55.
Basma G. Eid Thikryat Neamatallah Abeer Hanafy Hany M. El-Bassossy Lenah Binmahfouz Hibah M. Aldawsari Atif Hasan Gamal Abd El-Aziz Kiran Vemuri Alexandros Makriyannis 《Molecules (Basel, Switzerland)》2021,26(4)
The role of cannabinoid receptors in nephropathy is gaining much attention. This study investigated the effects of two neutral CB1 receptor antagonists, AM6545 and AM4113, on nephropathy associated with metabolic syndrome (MetS). MetS was induced in rats by high-fructose high-salt feeding for 12 weeks. AM6545, the peripheral silent antagonist and AM4113, the central neutral antagonist were administered in the last 4 weeks. At the end of study, blood and urine samples were collected for biochemical analyses while the kidneys were excised for histopathological investigation and transforming growth factor beta 1 (TGFβ1) measurement. MetS was associated with deteriorated kidney function as indicated by the elevated proteinuria and albumin excretion rate. Both compounds equally inhibited the elevated proteinuria and albumin excretion rate while having no effect on creatinine clearance and blood pressure. In addition, AM6545 and AM4113 alleviated the observed swelling and inflammatory cells infiltration in different kidney structures. Moreover, AM6545 and AM4113 alleviated the observed histopathological alterations in kidney structure of MetS rats. MetS was associated with a ten-fold increase in urine uric acid while both compounds blocked this increase. Furthermore, AM6545 and AM4113 completely prevented the collagen deposition and the elevated expression of the TGFβ1 seen in MetS animals. In conclusion, AM6545 and AM4113, possess reno-protective effects by interfering with TGFβ1-mediated renal inflammation and fibrosis, via peripheral action. 相似文献
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58.
Nutthapoom Pathomthongtaweechai Sunhapas Soodvilai Rath Pichyangkura Chatchai Muanprasat 《Molecules (Basel, Switzerland)》2020,25(23)
Chitosan oligosaccharide (COS), a natural polymer derived from chitosan, exerts several biological activities including anti-inflammation, anti-tumor, anti-metabolic syndrome, and drug delivery enhancer. Since COS is vastly distributed to kidney and eliminated in urine, it may have a potential advantage as the therapeutics of kidney diseases. Polycystic kidney disease (PKD) is a common genetic disorder characterized by multiple fluid-filled cysts, replacing normal renal parenchyma and leading to impaired renal function and end-stage renal disease (ESRD). The effective treatment for PKD still needs to be further elucidated. Interestingly, AMP-activated protein kinase (AMPK) has been proposed as a drug target for PKD. This study aimed to investigate the effect of COS on renal cyst enlargement and its underlying mechanisms. We found that COS at the concentrations of 50 and 100 µg/mL decreased renal cyst growth without cytotoxicity, as measured by MTT assay. Immunoblotting analysis showed that COS at 100 µg/mL activated AMPK, and this effect was abolished by STO-609, a calcium/calmodulin-dependent protein kinase kinase beta (CaMKKβ) inhibitor. Moreover, COS elevated the level of intracellular calcium. These results suggest that COS inhibits cyst progression by activation of AMPK via CaMKKβ. Therefore, COS may hold the potential for pharmaceutical application in PKD. 相似文献
59.
Edson Hideaki Yoshida Murilo Melo Juste Dini Jessica Campanholi José Carlos Cogo Denise Grotto Stephen Hyslop 《Natural product research》2020,34(17):2533-2538
AbstractWe examined the ability of Bothrops jararaca venom (12.5?mg/kg) injected intraperitoneally (i.p.) to cause acute kidney injury (AKI) in rats. Blood urea and creatinine (AKI biomarkers, in g dL?1) were elevated after 2?h in venom-treated rats (urea: from 0.41?±?0.1 to 0.7?±?0.03; creatinine from 46.7?±?3.1 to 85?±?6.7; p?<?0.05; n?=?3 each), with no change in circulating reduced glutathione. Venom-treated rats survived for ~6?h, at which point platelets were reduced (×103 µL?1; from 763.8?±?30.2 to 52.5?±?18.2) whereas leukocytes and erythrocytes were slightly increased (from 4.7?±?0.3 to 6.6?±?0.1?×?103?µL?1 and from 8.38?±?0.1 to 9.2?±?0.09?×?106?µL?1, respectively; p?<?0.05); blood protein (5.2?±?0.4?g dL?1) and albumin (2.7?±?0.1?g dL?1) were normal, whereas blood and urinary urea and creatinine were increased. All parameters returned to normal with antivenom given 2?h post-envenomation. The i.p. injection of venom caused AKI similar to that seen with other routes of administration. 相似文献
60.
Iga Stryjak Natalia Warmuziska Joanna Bogusiewicz Kamil uczykowski Barbara Bojko 《Journal of separation science》2020,43(9-10):1867-1878
The limiting factor in conventional quality assessments of transplanted organs, namely the invasiveness of tissue sample collection, has prompted much research on the field of transplantology to focus on the development of alternative evaluation methods of organ quality. In the present project, we undertake the challenge to address the need for a new analytical solution for graft quality assessments by using a novel metabolomic diagnostic protocol based on low‐invasive solid‐phase microextraction. Solid‐phase microextraction probes of ca. 0.2 mm coated with 4 mm long mixed‐mode extraction phase were inserted into rabbit kidneys immediately following euthanasia and after 2, 4, 6, and 21 h of preservation. Liquid chromatography–mass spectrometry analysis of the extracts was performed with the use of a reversed phase column and a Q‐Exactive Focus mass spectrometer operated in positive ionization mode. Statistical analysis of significantly changing compounds revealed metabolic profile changes in kidneys induced by ischemia and oxidative stress as a function of the duration of cold storage. The most pronounced alterations were reflected in levels of essential amino acids and purine nucleosides. Our findings demonstrate that the proposed approach may be successfully used to monitor changes in the metabolic profile of organs over time of preservation. 相似文献