Evidence map›Paper›PMID 36042482›Full record

ArticleChinese medicine2022

Traditional Chinese Medicine Fufang-Zhenzhu-Tiaozhi capsule prevents renal injury in diabetic minipigs with coronary heart disease.

Lixia Song, Ke Wang, Jianying Yin, Yiqi Yang, Bo Li, Dongxing Zhang, Hong Wang, Weixuan Wang, Wenjing Zhan, Caijuan Guo and 6 more

Open access · goldAbstract read
In one paragraph

Article in Chinese medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 2 institutions in 1 country.

Lixia Song *Guangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Ke Wang *Guangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Jianying Yin *Guangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Yiqi Yang *Guangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Bo LiGuangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Dongxing ZhangGuangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Hong WangGuangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Weixuan WangGuangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Wenjing ZhanKey Laboratory of Glucolipid Metabolic Disorder, Ministry of Education of China, Guangdong, China.
Caijuan GuoGuangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Zhanhui GuGuangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Lexun WangGuangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Zhihuan ZengDepartment of Cardiovascular Diseases, the First Affiliated Hospital of Guangdong Pharmaceutical University, Guangdong, China.
Weijian BeiGuangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China. 13660020495@139.com.ORCID http://orcid.org/0000-0002-5135-3274
Xianglu RongGuangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China.
Jiao GuoGuangdong Metabolic Disease Research Center of Integrated Chinese and Western Medicine, Guangdong, China. gyguoyz@163.com.
Ministry of Education of the People's Republic of China · CNFirst Affiliated Hospital of Guangdong Pharmaceutical University · CN

Funding

Basic and Applied Basic Research Foundation of Guangdong Province 2019A1515110123Basic and Applied Basic Research Foundation of Guangdong Province 2021A1515012553Guangdong Provincial TCM Administration Department Grant 20151269Innovative Strong School Project of Guangdong Pharmaceutical University 2018KQNCX130Medical Science and Technology Foundation of Guangdong Province A2019531National Natural Science Foundation of China 81530102the international cooperation base for the prevention and treatment of metabolic diseases 2016B050501003
6 · The paper itself

Abstract

backgroundRenal injury is one of the common microvascular complications of diabetes, known as diabetic kidney disease (DKD) seriously threatening human health. Previous research has reported that the Chinese Medicine Fufang-Zhenzhu-Tiaozhi (FTZ) capsule protected myocardia from injury in diabetic minipigs with coronary heart disease (DM-CHD). And we found significant renal injury in the minipigs. Therefore, we further investigated whether FTZ prevents renal injury of DM-CHD minipig and H

methodsDM-CHD model was established by streptozotocin injection, high fat/high-sucrose/high-cholesterol diet combined with balloon injury in the coronary artery. Blood lipid profile, fasting blood glucose (FBG), and SOD were measured with kits. The levels of blood urea nitrogen (BUN), serum creatinine (Scr), urine trace albumin (UALB), urine creatinine (UCR) (calculate UACR), cystatin (Cys-C), and β-microglobulin (β-MG) were measured by ELISA kits to evaluate renal function. TUNEL assay was performed to observe the apoptosis. qPCR was used to detect the mRNA expression levels of HO-1, NQO1, and SOD in kidney tissue. The protein expressions of Nrf2, HO-1, NQO1, Bax, Bcl-2, and Caspase 3 in the kidney tissue and HK-2 cells were detected by western blot. Meanwhile, HK-2 cells were induced by H

resultsIn DM-CHD minipigs, blood lipid profile and FBG were elevated significantly, and the renal function was decreased with the increase of BUN, Scr, UACR, Cys-c, and β-MG. A large number of inflammatory and apoptotic cells in the kidney were observed accompanied with lower levels of SOD, Bcl-2, Nrf2, HO-1, and NQO1, but high levels of Bax and Cleaved-caspase 3. FTZ alleviated glucose-lipid metabolic disorders and the pathological morphology of the kidney. The renal function was improved and the apoptotic cells were reduced by FTZ administration. FTZ could also enhance the levels of SOD, Nrf2, HO-1, and NQO1 proteins to promote antioxidant effect, down-regulate the expression of Bax and Caspase3, as well as up-regulate the expression of Bcl-2 to inhibit cell apoptosis in the kidney tissue and HK-2 cells.

conclusionsWe concluded that FTZ prevents renal injury of DM-CHD through activating anti-oxidative capacity to reduce apoptosis and inhibiting inflammation, which may be a new candidate for DKD treatment.

Indexed as

ApoptosisDiabetesFufang-Zhenzhu-Tiaozhi (FTZ)Oxidative stressRenal injury

Identifiers

PMID36042482
PMCPMC9429629
OpenAlexW4293568953

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.