Objective: To observe the effects of swimming training and/or epigallocatechin gallate(EGCG) on the expression of myocardial interstitial protein and its relationship with transforming growth factor-beta(TGF-β)/Smads signaling pathway in type 2 diabetic rats.
Methods: Male SD rats(SPF grade, 6 weeks old) were fed with high-fat diet for 6 weeks and intraperitoneal injection of streptozotocin(STZ, 30 mg/kg). The rats were randomly divided into four groups: diabetic model group(D), diabetes EGCG group(DG), diabetes exercise group(DE), and diabetes exercise EGCG group(DEG), with 8 rats in each group, and 6 male SD rats in the same batch were added as the normal C group. The rats in the exercise group were given swimming training without load. The swimming time was 15 min/d in the first week, and the time was increased by 15 min a week until it was extended to 90 min/d. The rats in the exercise group were trained for 5 days a week. Rats in the EGCG group(100 mg/kg BW) were intragastrical administered for 7 days. Swimming training and/or EGCG intervention lasted for 12 weeks. 48 hours after the end of the intervention experiment, the rats were fasted overnight for 12 hours. Myocardial collagen I(Col I), collagen IV(Col IV) and fibronectin(FN) protein expression were detected by immunohistochemistry in some left ventricles, hydroxyproline(Hyp) content was detected by colorimetry, TGF-β_1 protein expression was detected by WB, Smad2 and Smad7 mRNA expression were detected by RT-PCR.
Results: The levels of blood glucose, Hyp content, TGF-beta1, Smad2 mRNA, Col I, Col IV, FN of the rats from D group were significantly higher than those of the rats from C group(P<0. 01), but the level of Smad7 mRNA was significantly lower than it of the rats from C group(P<0. 01). Compared with D group, blood glucose, TGF-β_1, Smad2 mRNA expression, Hyp content, Col I, Col IV, FN protein expression in DG group, DE group and DEG group were significantly decreased(P<0. 05 or P<0. 01), and the Smad7 mRNA expression increased significantly(P<0. 05 or P<0. 01). Compared with DG group, blood glucose, Smad2 mRNA expression, Hyp content, Col I, Col IV protein expression in DEG group were significantly decreased(P<0. 05 or P<0. 01), and the myocardial Smad7 mRNA expression was significantly increased(P<0. 05). Compared with DE group, the levels of blood glucose, TGF-β_1, Smad2 mRNA, Hyp content, Col I, Col IV protein expression were significantly decreased in the EGCG group(P<0. 05 or P<0. 01), and the expression of Smad7 mRNA was significantly increased(P<0. 05). Blood glucose, Smad2 mRNA expression, Hyp content, Col I, Col Ⅳ, FN protein expression in(DEG group were significantly higher than those in C group(P<0. 05 or P<0. 01).
Conclusion: 12 weeks swimming training and/or EGCG administration can reduce the expression of myocardial interstitial protein in type 2 diabetic rats, and the combined intervention effect is better.
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http://dx.doi.org/10.19813/j.cnki.weishengyanjiu.2021.01.015 | DOI Listing |
Exp Hematol Oncol
January 2025
Department of Hematology, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Myelodysplastic Syndromes (MDS) represent a group of heterogeneous myeloid clonal diseases derived from aberrant hematopoietic stem/progenitor cells. Enhancer of zeste homolog 2 (EZH2) is an important regulator in gene expression through methyltransferase-dependent or methyltransferase-independent mechanisms. Herein, we found EZH2 inhibition led to MDS cell pyroptosis through RNA Helicase A (RHA) down-regulation induced overexpression of S100A9, a key regulator of inflammasome activation and pyroptosis.
View Article and Find Full Text PDFJ Orthop Surg Res
January 2025
Linyi People's Hospital postgraduate training base of Guangzhou University of Traditional Chinese Medicine, Linyi, Shandong, 276000, China.
Background: The endoplasmic reticulum stress (ER stress) has been involved in various musculoskeletal disorders including non-traumatic osteonecrosis of femoral head (NT-ONFH).
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Methods: We enrolled NT-ONFH patients (n = 150) alongside healthy controls (HCs, n = 150).
J Exp Clin Cancer Res
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Department of General Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, 410008, China.
Background: Colorectal cancer (CRC) has high incidence and mortality rates, with severe prognoses during invasion and metastasis stages. Despite advancements in diagnostic and therapeutic technologies, the impact of the tumour microenvironment, particularly extracellular matrix (ECM) stiffness, on CRC progression and metastasis is not fully understood.
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BMC Pulm Med
January 2025
Department of Respiratory Medicine, Faculty of Life Sciences, Kumamoto University, Kumamoto 1-1-1 Honjo, Chuo-ku, 860-8556, Japan.
Background: Fibrotic types of interstitial lung abnormalities seen on high-resolution computed tomography scans, characterised by traction bronchiolectasis/bronchiectasis with or without honeycombing, are predictors of progression and poor prognostic factors of interstitial lung abnormalities. There are no reports on the clinical characteristics of fibrotic interstitial lung abnormalities on high-resolution computed tomography scans. Therefore, we aimed to examine these clinical characteristics and clarify the predictive factors of fibrotic interstitial lung abnormalities on high-resolution computed tomography scans.
View Article and Find Full Text PDFCell Commun Signal
January 2025
Laboratory of Veterinary Clinical Pharmacology, College of Veterinary Medicine, Inner Mongolia Agricultural University, No. 306, Zhaowuda Road, Hohhot, 010018, China.
Wound healing is a highly coordinated process driven by intricate molecular signaling and dynamic interactions between diverse cell types. Nod-like receptor pyrin domain-containing protein 3 (NLRP3) has been implicated in the regulation of inflammation and tissue repair; however, its specific role in skin wound healing remains unclear. This study highlights the pivotal role of NLRP3 in effective skin wound healing, as demonstrated by delayed wound closure and altered cellular and molecular responses in NLRP3-deficient (NLRP3) mice.
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