ABSTRACT
This study aimed to explore the effects of Shenyuan granules on the Klotho/FGFR23/Egr1 signaling pathway and calcium-phosphorus metabolism in diabetic mice models with impairment of renal function. Streptozotocin-induced diabetic nephropathy (DN) mice models were randomly divided into three groups: Shenyuan granules group (n=10), model control group (n=10), and blank control group (n=10). Corresponding drugs were given by gavage for 8 weeks. Blood glucose and serum creatinine (SCr), urea nitrogen (BUN), calcium (Ca), phosphorus (P) and mLAB were detected before and after administration. Moreover, RT-qPCR was performed to detect the expression of CYP24 and CYP27 mRNA in kidney tissue. Blood FGF23 was detected by ELISA. Western-blot and immunohistochemistry were performed to detect the expressions of Klotho, FGFR1, Egr1, CYP24, CYP27, ERK1/2 and p-ERK1/2. Compared with the blank control group, in the model control group serum FGF23,P, SCr and 24-hour proteinuria levels increased (P<0.05), serum Ca significantly decreased (P<0.05), expressionss of Egr1, CYP24, CYP27 and p-ERK1/2 were up-regulated (P<0.05), and the expressions of Klotho and FGFR1 were down-regulated (P<0.05). After treatment, compared with the model control group, in the Shenyuan granule group serum FGF23, P, SCr levels decreased (P<0.05), serum Ca increased (P<0.05), expressions of Egr-1, CYP24, CYP27 and p-ERK1/2 were down-regulated (P<0.05), and the expressions of Klotho and FGFR1 were up-regulated (P<0.05). Shenyuan granules may partly intervene in the expressions of CYP24 and CYP27 through the Klotho/FGF23/Egr1 signaling pathway, thereby improving calcium and phosphorus metabolism and alleviating renal injury in diabetic nephropathy.
Subject(s)
Calcium/metabolism , Diabetic Nephropathies/drug therapy , Drugs, Chinese Herbal/pharmacology , Phosphorus/metabolism , Signal Transduction , Animals , Cytochrome P450 Family 24/metabolism , Cytochrome P450 Family 27/metabolism , Diabetes Mellitus, Experimental/drug therapy , Early Growth Response Protein 1/metabolism , Fibroblast Growth Factor-23 , Fibroblast Growth Factors/metabolism , Glucuronidase/metabolism , Kidney/pathology , Klotho Proteins , MiceABSTRACT
BACKGROUND: The enlarged mediastinal lymph nodes caused by tuberculosis (TB) and chronic lymphocytic leukaemia (CLL) are similar, sometimes resulting in misdiagnosis of the two diseases. OBJECTIVE: To determine the differential characteristics of enlarged mediastinal lymph nodes caused by TB and CLL using multidetector-row computed tomography (MDCT). MATERIALS AND METHODS: We conducted a retrospective analysis for the anatomical distribution and enhancement patterns of mediastinal lymph nodes on MDCT in 67 consecutive patients with newly diagnosed untreated TB (58%) and CLL (42%). RESULTS: Concerning the main anatomic distribution of lymph nodes, TB involved the 4R (n = 32, 82%) and 10R (n = 27, 69%) regions more often than CLL (n = 16, 57%; n = 12, 43%, respectively). Contrast region 1 had a greater tendency to be affected in CLL (n = 16, 57%) than TB (n = 11, 28%). TB showed peripheral enhancement in 28 cases (72%), frequently with a multilocular appearance, compared to CLL, which showed no peripheral enhancement in these cases. Homogeneous enhancement was more commonly seen in CLL than in TB (82% vs. 10%, P < 0.01). CONCLUSION: The distribution and enhancement pattern of enlarged lymph nodes on MDCT was useful in differentiating TB and CLL.
Subject(s)
Leukemia, Lymphocytic, Chronic, B-Cell/diagnostic imaging , Lymph Nodes/diagnostic imaging , Multidetector Computed Tomography , Tuberculosis, Lymph Node/diagnostic imaging , Adult , Aged , Diagnosis, Differential , Female , Humans , Male , Mediastinum , Middle Aged , Predictive Value of Tests , Retrospective StudiesABSTRACT
2-Aminopyridines 1a-c and 1-aminoisoquinoline with 1-chloromethylbenzotriazole give 2-amino-1-[alpha-benzotriazol-1-ylmethyl]pyridinium chlorides 2a-c and 1-amino-2-(alpha-benzotriazol-1-ylmethyl)isoquinolinium++ + chloride 12, respectively. Compounds 2a-c and 12 react with aryl aldehydes 3a-h to afford imidazolo[1,2-a]pyridines 7a-k and imidazolo[2, 1-a]isoquinolines 13a,b in good yields.