School of Pharmacy, Xinxiang Medical University, Xinxiang, P. R. China.
Xinxiang Key Laboratory of Clinical Psychopharmacology, Xinxiang Medical University, Xinxiang, P. R. China.
Pharm Biol. 2023 Dec;61(1):710-721. doi: 10.1080/13880209.2023.2201606.
Danggui Buxue Decoction (DBD) is an effective complementary medicine in alleviating myelosuppression after chemotherapy (MAC). However, its mechanism of action is elusive.
To illustrate that regulating β-hydroxybutyric acid (β-OHB) metabolism and suppressing oxidative stress could be a potential mechanism of action for DBD in alleviating MAC.
After HPLC quantification and dose testing (3, 6 and 10 g/kg, gavage) of DBD, Sprague-Dawley rats were divided into control, cyclophosphamide (CTX) (30 mg/kg CTX for 5 days, intraperitoneal administration) and CTX + DBD groups (6 g/kg DBD for 14 days, gavage). Blood cell counts, thigh bone histological examination, β-OHB levels, oxidative stress indices and HDAC1 activity were tested. The biological function of β-OHB was verified (hBMSC cells were incubated in culture mediums that contained 40 μM CTX and β-OHB in 0, 1, 2.5, 5, 10 mM) and (MAC rat model, 3 g/kg β-OHB for 14 days, gavage).
Rats in the CTX + DBD group showed upregulated blood cell counts (118-243%), β-OHB levels (495 nmol/mL in blood, 122 nmol/mg in marrow supernatant) and downregulated HDAC1 activity (59%), and oxidative stress indices (60-85%). , 5 mM β-OHB improved hBMSC cell migration (123%) and proliferation (131%). , rats treated with 3 g/kg β-OHB showed upregulated blood cell counts (121-182%) and downregulated HDAC1 activity (64%) and oxidative stress indices (65-83%).
DBD, a traditional Chinese medicine, alleviates MAC by intervening in β-OHB metabolism and oxidative stress.
当归补血汤(DBD)是一种缓解化疗后骨髓抑制(MAC)的有效辅助药物。但其作用机制尚不清楚。
阐述调节β-羟丁酸(β-OHB)代谢和抑制氧化应激可能是 DBD 缓解 MAC 的潜在作用机制。
采用高效液相色谱法(HPLC)定量和剂量测试(3、6 和 10 g/kg,灌胃)DBD 后,将 Sprague-Dawley 大鼠分为对照组、环磷酰胺(CTX)组(CTX 30 mg/kg,连续 5 天腹腔注射)和 CTX+DBD 组(DBD 6 g/kg,连续 14 天灌胃)。检测血细胞计数、大腿骨组织学检查、β-OHB 水平、氧化应激指标和 HDAC1 活性。验证了β-OHB 的生物学功能(在含有 40 μM CTX 和β-OHB 的 0、1、2.5、5、10 mM 的培养基中孵育 hBMSC 细胞)和(MAC 大鼠模型,灌胃 3 g/kgβ-OHB,连续 14 天)。
CTX+DBD 组大鼠的血细胞计数(118-243%)、β-OHB 水平(血液中 495 nmol/mL,骨髓上清液中 122 nmol/mg)和 HDAC1 活性(59%)均升高,氧化应激指标(60-85%)降低。,5 mMβ-OHB 可提高 hBMSC 细胞迁移(123%)和增殖(131%)。,灌胃 3 g/kgβ-OHB 的大鼠血细胞计数(121-182%)升高,HDAC1 活性(64%)和氧化应激指标(65-83%)降低。
DBD 作为一种中药,通过干预β-OHB 代谢和氧化应激缓解 MAC。