Gu Jianhong, Liu Dan, Gong Anqing, Zhao Xinrui, Zhou Jiatao, Wang Panting, Xia Han, Song Ruilong, Ma Yonggang, Zou Hui, Memon Muhammad Azhar, Yuan Yan, Liu Xuezhong, Bian Jianchun, Liu Zongping, Tong Xishuai
College of Veterinary Medicine, Joint International Research Laboratory of Agriculture and Agri-Product Safety of the Ministry of Education of China, Yangzhou University, Yangzhou 225009, China.
Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, China.
Vet Sci. 2025 Mar 31;12(4):317. doi: 10.3390/vetsci12040317.
Cadmium (Cd) is a toxic, non-essential metal that primarily enters animal bodies through the digestive and respiratory systems, leading to damage to multiple organs and tissues. Cd can accumulate in cartilage and induce damage to chondrocytes. Procyanidins (PAs), also known as concentrated tannic acid or oligomeric proanthocyanidins (OPCs), exhibit diverse biological and pharmacological activities. However, the mechanism of OPCs alleviates Cd-induced damage to chondrocytes in chickens remains to be further explored in vitro. Chondrocytes were isolated from both ends of the tibia of 17-day-old SPF chicken embryos, and then subsequently treated with various concentrations of Cd (0, 1, 2.5, 5, and 10 μmol/L) or OPCs (0, 5, 10, 20, and 40 μmol/L) to investigate the mechanism underlying extracellular matrix (ECM) degradation and damage. Cd reduced cell viability, glycosaminoglycan (GAG) secretion, and ECM degradation in chondrocytes by decreasing the expression of type II collagen alpha 1 (COL2A1) and aggrecan (ACAN) while increasing the release of cartilage oligomeric matrix protein (COMP), along with elevated levels of matrix-degrading enzymes, such as matrix metalloproteinases 1 (MMP1), MMP10, and MMP13, and a disintegrin and metalloproteinase with thrombospondin motifs 4 (ADAMTS4) and ADAMTS5. Cd induced phosphorylation of extracellular signal-regulated kinases 1/2 (ERK1/2) and the expression of matrix-degrading enzymes, impairing ECM synthesis, an effect that could be alleviated by ERK1/2 inhibitor U0126. Chondrocytes were treated with 5 μmol/L Cd and 10 μmol/L OPCs, and it was found that OPCs inhibited the activation of the ERK1/2 signaling pathway and the expression of matrix-degrading enzymes, while promoting ECM synthesis and alleviating Cd-induced ECM damage in chickens. This study provides a theoretical basis for clinical research on OPCs with respect to the prevention and treatment of Cd-induced chondrogenic diseases in poultry.
镉(Cd)是一种有毒的非必需金属,主要通过消化系统和呼吸系统进入动物体内,导致多个器官和组织受损。Cd可在软骨中蓄积并诱导软骨细胞损伤。原花青素(PAs),也称为浓缩单宁酸或低聚原花青素(OPCs),具有多种生物学和药理活性。然而,OPCs减轻Cd诱导的鸡软骨细胞损伤的机制仍有待在体外进一步探索。从17日龄SPF鸡胚胫骨两端分离软骨细胞,随后用不同浓度的Cd(0、1、2.5、5和10μmol/L)或OPCs(0、5、10、20和40μmol/L)处理,以研究细胞外基质(ECM)降解和损伤的潜在机制。Cd通过降低II型胶原α1(COL2A1)和聚集蛋白聚糖(ACAN)的表达,同时增加软骨寡聚基质蛋白(COMP)的释放,以及提高基质降解酶如基质金属蛋白酶1(MMP1)、MMP10和MMP13,以及含血小板反应蛋白基序的解聚素和金属蛋白酶4(ADAMTS4)和ADAMTS5的水平,降低软骨细胞的活力、糖胺聚糖(GAG)分泌和ECM降解。Cd诱导细胞外信号调节激酶1/2(ERK1/2)磷酸化和基质降解酶的表达,损害ECM合成,而ERK1/2抑制剂U0126可减轻这种效应。用5μmol/L Cd和10μmol/L OPCs处理软骨细胞,发现OPCs抑制ERK1/2信号通路的激活和基质降解酶的表达,同时促进ECM合成并减轻Cd诱导的鸡ECM损伤。本研究为OPCs预防和治疗家禽Cd诱导的软骨生成性疾病的临床研究提供了理论依据。