Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
1.
Chinese Journal of Experimental Traditional Medical Formulae ; (24): 32-37, 2022.
Article in Chinese | WPRIM | ID: wpr-940483

ABSTRACT

ObjectiveTo observe the intervention of modified Sanrentang on the lipopolysaccharide-induced proliferation of rat glomerular mesangial cells, the phosphatidylinositol-3 kinase(PI3K)/protein kinase B(PKB/Akt)/nuclear factor kappa B(NF-κB) signaling pathway, and to investigate its mechanism in improving kidney inflammation in rats with immunoglobulin A nephropathy(IgAN). MethodThe 18 rats were divided into 3 groups by serum pharmacology method: normal group, high-dose and low-dose (20.70,10.35 g·kg-1·d-1) groups with 6 rats in each group. Modified Sanrentang high- and low-dose groups were intragastric with the corresponding solution of modified Sanrentang, and normal group was intragastric with equal volume of distilled water. After 5 days of intragastric administration, blood samples were collected to prepare drug-containing serum. Rat mesangial (HBZY-1) were divided into five groups of normal group, LPS 10 mg·L-1 in the model group, benazepril(50 μmol·L-1), modified Sanrentang high- and low-dose group. Preclude the use of methyl thiazolyl tetrazolium(MTT) method detect the proliferation activity of HBZY-1 cells, enzyme-linked immunosorbent assay(ELISA) was used to determine the content of each group type Ⅳ collagen(ColⅣ),Western blot and Real-time fluorescence quantitative polymerase chain reaction(Real-time PCR) were used to detect protein and mRNA expression levels of PI3K/Akt/NF-κB signaling pathway. ResultAs compared with the normal group, MTT assay showed that exposure to LPS significantly enhanced the proliferative activity, the ColⅣ was increased significantly of HBZY-1 cells(P<0.01), p-Akt, p-p65 was increased significantly (P<0.01). Compared with the model group, the proliferation and ColⅣ of rat chronic glomerulonephritis cells induced by LPS by inhibiting PI3K/Akt/NF-κB signaling pathway(P<0.01), and the phosphorylation of Akt was significantly inhibited(P<0.01), the expression levels of NF-κB p65 was reduced in modified Sanrentang high-dose group(P<0.01). ConclusionModified Sanrentang could inhibit cell proliferation and the content of ColⅣ in rat mesangial cells induced by LPS, and its mechanism might be related to suppression of PI3K/Akt signaling pathway.

2.
Chinese Journal of Experimental Traditional Medical Formulae ; (24): 16-22, 2022.
Article in Chinese | WPRIM | ID: wpr-940346

ABSTRACT

ObjectiveTo study the effect and mechanism of Wuwei Xiaoduyin in treating rat renal mesangial cells (HBZY-1) induced by lipopolysaccharide (LPS) through the nuclear factor-κB (NF-κB) signaling pathway. MethodRat HBZY-1 cells were randomly assigned into the normal group, model group, benazepril (50 μmol·L-1) group, and high- and low-dose (2.75 and 0.69 g·kg-1) Wuwei Xiaoduyin groups. The normal group, model group, and benazepril group were treated with 10% normal rat serum, and the Wuwei Xiaoduyin groups with 10% medicated serum. Except the normal group, the other four groups were treated with LPS (100 ng·mL-1) for modeling in vitro. The changes of cell morphology were observed under optical microscope. The expression of NF-κB p65 was detected by immunofluorescence (IF) method. Methyl thiazolyl tetrazolium (MTT) colorimetry was employed to detect cytotoxicity and cell proliferation. The levels of interleukin-1β (IL-1β), intercellular adhesion molecule-1 (ICAM-1), laminin (LN), and fibronectin (FN) in cell supernatant were determined by enzyme-linked immunosorbent assay (ELISA). The mRNA levels of IL-1β, FN, and NF-κB p65 were measured by real-time fluorescence quantitative PCR. The protein levels of phosphorylated inhibitor of NF-κB kinase β (p-IKKβ), phosphorylated NF-κB inhibitor (p-IκBα), and NF-κB p65 were determined by Western blot. ResultCompared with the normal group, the modeling increased cell proliferation (P<0.01), elevated the levels of IL-1β, ICAM-1, LN, and FN in cell supernatant (P<0.01), and up-regulated the mRNA levels of IL-1β, FN, and NF-κB p65 (P<0.01) and the protein levels of p-IKKβ, p-IκBα, and NF-κB p65 (P<0.01). Such changes were recovered by benazepril and Wuwei Xiaoduyin (P<0.05, P<0.01). ConclusionWuwei Xiaoduyin can mitigate the inflammatory injury of renal mesangial cells induced by LPS by inhibiting the NF-κB signaling pathway.

3.
Chinese Journal of Experimental Traditional Medical Formulae ; (24): 15-22, 2021.
Article in Chinese | WPRIM | ID: wpr-906480

ABSTRACT

Objective:To observe the effect of Wuwei Xiaoduyin on the nuclear factor-<italic>κ</italic>B (NF-<italic>κ</italic>B) signaling pathway in immunoglobulinA nephropathy(IgAN) rats, and to explore its mechanism of action in the treatment of IgA nephropathy. Method:The 40 SD rats were randomly divided into control group, model group, benazepril group (10 mg·kg·d<sup>-1</sup>) and Wuwei Xiaoduyin group (2.75 g·kg·d<sup>-1</sup>), with 10 rats in each group. The IgA nephropathy rat model was established by intragastric administration of bovine serum albumin (BSA), subcutaneous injection of carbon tetrachloride (CCl<sub>4</sub>) and tail vein injection of lipopolysaccharide (LPS) for 9 weeks. The rats in each group were given corresponding doses of drugs by gavage, while the rats in the control group and model group were given the same amount of normal saline for successive 28 days. The levels of 24-hour urinary protein (UTP), serum creatinine (SCr), blood urea nitrogen (BUN) and serum albumin (ALB) were detected. The contents of tumor necrosis factor-<italic>α</italic> (TNF-<italic>α</italic>), interleukin-1<italic>β</italic> (IL-1<italic>β</italic>) and interleukin-6 (IL-6) in serum were detected by enzyme-linked immunosorbent assay (ELISA), the hematoxylineosin staining (HE), immunofluorescence and transmission electron microscopy were used to observe the renal pathological changes, the expressions of IL-6, I<italic>κ</italic>B kinase <italic>β</italic> (IKK<italic>β</italic>), phosphorylated I<italic>κ</italic>B kinase <italic>β</italic> (p-IKK<italic>β</italic>), NF-<italic>κ</italic>B inhibitor protein <italic>α</italic> (I<italic>κ</italic>B<italic>α</italic>), phosphorylated NF-<italic>κ</italic>B inhibitor protein <italic>α</italic> (p-I<italic>κ</italic>B<italic>α</italic>), NF-<italic>κ</italic>B p65 and p-NF-<italic>κ</italic>B p65 were detected by immunohistochemistry (IHC), real-time PCR (RT-PCR) and Western blot, respectively. Result:Compared with the control group, the level of UTP in the model group significantly increased (<italic>P</italic><0.01), cultured glomerular mesangial cells proliferated, mesangial matrix and electronic dense deposit increased, mesentery thickened. A large amount of IgA was deposited in the glomerular mesangial area and showed irregular particles and mass distribution, the levels of TNF-<italic>α</italic>, IL-1<italic>β</italic>, IL-6 in serum significantly increased (<italic>P</italic><0.01), the expression levels of IL-6, IKK<italic>β</italic>, p-IKK<italic>β, </italic>NF-<italic>κ</italic>B p65 and p-NF-<italic>κ</italic>B p65 in renal tissue significantly increased (<italic>P</italic><0.01).Compared with the model group, the levels of UTP in each administration group significantly decreased (<italic>P</italic><0.01), and the renal tissue injury alleviated, the levels of TNF-<italic>α</italic>, IL-1<italic>β</italic>, IL-6 in serum significantly decreased (<italic>P</italic><0.01), the expressions of IL-6, IKK<italic>β</italic>, p-IKK<italic>β</italic>, I<italic>κ</italic>B<italic>α</italic>, p-I<italic>κ</italic>B<italic>α</italic>, NF-<italic>κ</italic>B p65 and p-NF-<italic>κ</italic>B p65 in the renal tissue significantly decreased (<italic>P</italic><0.01). There were no significant differences in serum creatinine, blood urea nitrogen and serum albumin among the groups. Conclusion:Wuwei Xiaoduyin can reduce proteinuria in IgA nephropathy rats, and its mechanism may be related to the inhibition of NF-<italic>κ</italic>B signaling pathway and the over expression of related inflammatory factors.

4.
China Journal of Orthopaedics and Traumatology ; (12): 568-572, 2021.
Article in Chinese | WPRIM | ID: wpr-888317

ABSTRACT

OBJECTIVE@#To explore the clinical effect of manual reduction combined with homemade splint external fixation in the treatment of metacarpal fractures.@*METHODS@#A retrospective analysis was performed in 126 patients with metacarpal fracture treated by manual reduction and homemade splint external fixation in the emergency department of our hospital from January 2018 to December 2018, including 102 male, 24 female, ranging in age from 9 to 73 year old, with an average of (33.2±14.3)years old. During the treatment, the X-ray was re-examined regularly, and the external fixation was continued or adjusted according to the X-ray situation. The X-ray showed callus growth. After the fracture was stable, the external fixation was removed to continue functional exercise. The TAM scoring standardwas used to evaluate the hand function, and the fracture healing and complications were summarized.@*RESULTS@#Of the 126 patients, 6 patients were treated with operation because of fracture displacement during the treatment. The other 120 patients were treated with this method and all of them got bony healing. The healing time was (6.3±1.8) weeks. The follow up time ranged from 2 to 12 months, with a mean of (4.4±2.2) months. At the latest follow up, TAM score was used to evaluate the hand function:excellent in 105 cases, good in 13 cases, fair in 2 cases and poor in 0 case. Shortening deformity was found in 7 cases and angulation deformity in 3 cases.@*CONCLUSION@#Manual reduction combined with homemade splint external fixation in the treatment of metacarpal fractures can achieve good clinical results. Homemade splint is easy to obtain materials and low cost, and it is an effective method worthy of clinical promotion.


Subject(s)
Adolescent , Adult , Aged , Child , Female , Humans , Male , Middle Aged , Young Adult , External Fixators , Fracture Fixation , Fracture Fixation, Internal , Metacarpal Bones , Retrospective Studies , Splints , Treatment Outcome
5.
China Journal of Chinese Materia Medica ; (24): 2707-2709, 2012.
Article in Chinese | WPRIM | ID: wpr-338036

ABSTRACT

Traditional Chinese medicine injection(TCMI) is a new preparation developing recent years, which is spreading because of the significant effect. Doctors acquire information of medicine from the prospectuses mainly. But due to many reasons, there are a lot of shortcomings such as lack of items, unknown of composition, the narrow scope, etc. Unreasonable drug use in field and dose happened frequently. Adverse reactions are often reported. They restricted the use of TCMI severely. We must pay attention to the market evaluation of TCMI, and improve the prospectuses gradually on the basis of clinical evidence. One hand, the use of drugs can be reference to it. On the other hand, it can avoid unreasonable use of drugs. We have done it in order to contribute to the clinical application of TCMI.


Subject(s)
Humans , Drug Interactions , Drugs, Chinese Herbal , Injections , Medicine, Chinese Traditional , Product Surveillance, Postmarketing
6.
Chinese Journal of Physical Medicine and Rehabilitation ; (12)2003.
Article in Chinese | WPRIM | ID: wpr-683387

ABSTRACT

Objective To set up a new method of mild hypothermia via lateral ventricle in rabbits following traumatic brain injury (TBI). Methods Twenty-one New Zealand rabbits were used for this study. TBI was pro- duced with all the rabbits in anesthesia by using free-falling impact model. Animals were randomly divided into three groups: a TBI group, a mild hypothermia group (by perfusion of 25℃Ringer's solution via the lateral ventricle) and a control group. The contents of water and total sodium, potassium of the brain region close to traumatic brain tissue were detected and pathological changes were observed in three groups. Results The number of the injured neurons was increased significantly in both TBI group and mild hypothermia group than that in control group at 72 h after TBI (P

SELECTION OF CITATIONS
SEARCH DETAIL