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当归补血汤通过调节β-羟丁酸代谢和抑制氧化应激缓解环磷酰胺引起的骨髓抑制。

Danggui Buxue decoction alleviates cyclophosphamide-induced myelosuppression by regulating β-hydroxybutyric acid metabolism and suppressing oxidative stress.

机构信息

School of Pharmacy, Xinxiang Medical University, Xinxiang, P. R. China.

Xinxiang Key Laboratory of Clinical Psychopharmacology, Xinxiang Medical University, Xinxiang, P. R. China.

出版信息

Pharm Biol. 2023 Dec;61(1):710-721. doi: 10.1080/13880209.2023.2201606.

Abstract

CONTEXT

Danggui Buxue Decoction (DBD) is an effective complementary medicine in alleviating myelosuppression after chemotherapy (MAC). However, its mechanism of action is elusive.

OBJECTIVE

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.

MATERIALS AND METHODS

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).

RESULTS

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%).

DISCUSSION AND CONCLUSIONS

DBD, a traditional Chinese medicine, alleviates MAC by intervening in β-OHB metabolism and oxidative stress.

摘要

背景

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。

目的

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。

材料和方法

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)。

结果

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。

讨论与结论

DBD 作为一种中药,通过干预β-OHB 代谢和氧化应激缓解 MAC。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e4a/10132245/d84823e1f807/IPHB_A_2201606_F0001_C.jpg

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