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Pharmacokinetics and pharmacodynamics of rhubarb anthraquinones extract in normal and disease rats.
Biomed Pharmacother. 2017 Jul; 91:425-435.BP

Abstract

BACKGROUND

Anthraquinones extract from Rheum palmatum L. (rhubarb) including rhein, emodin, aloe-emodin, chrysophanol, physcion and sennoside A, has been widely used in China to treat various diseases.

OBJECTIVE

This study was designed to explore the pharmacokinetic and pharmacodynamic properties of rhubarb anthraquinones extract in diabetic nephropathy and acute liver injury rats.

METHODS

The diabetic nephropathy and acute liver injury rats were induced by intraperitoneal injection with streptozotocin (STZ) and carbon tetrachloride (CCL4), respectively. The rats were treated with different doses of rhubarb anthraquinones extract (37.5, 75 and 150mg/kg) as administration groups. For pharmacokinetics, the drug concentrations of rhubarb anthraquinones consisting of rhein, emodin, aloe-emodin, chrysophanol, physcion and sennoside A were determined. For pharmacodynamics, the anti-diabetic nephropathy and hepatoprotective effects were assessed under different dosage regimens.

RESULTS

The rhein, emodin, aloe-emodin, chrysophanol were considered as pharmacokinetic markers at three doses of rhubarb anthraquinones extract. In diabetic nephropathy rats, no obvious pharmacokinetic change of the four ingredients was observed compared with control rats. However, the plasma exposures of the four ingredients increased in acute liver injury rats compared with control rats. The serum creatinine (SCr), blood urea nitrogen (BUN) and urine protein (UP) values in diabetic nephropathy rats decreased compared with those in the model group, which suggested that rhubarb anthraquinones extract displayed certain therapeutic and preventive effects against the diabetic nephropathy. However, rhubarb anthraquinones extract cannot ameliorate the CCL4-induced liver injury under the three different dosage regimens.

CONCLUSION

There was no significant pharmacokinetic difference after a single oral administration of rhubarb anthraquinones extract between control and diabetic nephropathy rats. However, apparent pharmacokinetic differences were observed between control and liver injury rats. Also, rhubarb anthraquinones extract had beneficial effects on diabetic nephropathy rats, while no marked effect on liver injury rats under the same dosage regimens.

Authors+Show Affiliations

State Key Laboratory of Natural Medicines, Key Lab of Drug Metabolism & Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, China.State Key Laboratory of Natural Medicines, Key Lab of Drug Metabolism & Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, China.State Key Laboratory of Natural Medicines, Key Lab of Drug Metabolism & Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, China.State Key Laboratory of Natural Medicines, Key Lab of Drug Metabolism & Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, China.State Key Laboratory of Natural Medicines, Key Lab of Drug Metabolism & Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, China.State Key Laboratory of Natural Medicines, Key Lab of Drug Metabolism & Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, China. Electronic address: hhp_770505@hotmail.com.State Key Laboratory of Natural Medicines, Key Lab of Drug Metabolism & Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, China. Electronic address: cpu_haokun@aliyun.com.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

28475921

Citation

Li, Peijin, et al. "Pharmacokinetics and Pharmacodynamics of Rhubarb Anthraquinones Extract in Normal and Disease Rats." Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie, vol. 91, 2017, pp. 425-435.
Li P, Lu Q, Jiang W, et al. Pharmacokinetics and pharmacodynamics of rhubarb anthraquinones extract in normal and disease rats. Biomed Pharmacother. 2017;91:425-435.
Li, P., Lu, Q., Jiang, W., Pei, X., Sun, Y., Hao, H., & Hao, K. (2017). Pharmacokinetics and pharmacodynamics of rhubarb anthraquinones extract in normal and disease rats. Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie, 91, 425-435. https://doi.org/10.1016/j.biopha.2017.04.109
Li P, et al. Pharmacokinetics and Pharmacodynamics of Rhubarb Anthraquinones Extract in Normal and Disease Rats. Biomed Pharmacother. 2017;91:425-435. PubMed PMID: 28475921.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Pharmacokinetics and pharmacodynamics of rhubarb anthraquinones extract in normal and disease rats. AU - Li,Peijin, AU - Lu,Qianfeng, AU - Jiang,Wenjiao, AU - Pei,Xue, AU - Sun,Yilin, AU - Hao,Haiping, AU - Hao,Kun, Y1 - 2017/05/02/ PY - 2017/2/21/received PY - 2017/4/21/revised PY - 2017/4/24/accepted PY - 2017/5/6/pubmed PY - 2018/3/27/medline PY - 2017/5/6/entrez KW - Acute liver injury rats KW - Diabetic nephropathy rats KW - Pharmacodynamics KW - Pharmacokinetics KW - Rhubarb anthraquinones extract SP - 425 EP - 435 JF - Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie JO - Biomed Pharmacother VL - 91 N2 - BACKGROUND: Anthraquinones extract from Rheum palmatum L. (rhubarb) including rhein, emodin, aloe-emodin, chrysophanol, physcion and sennoside A, has been widely used in China to treat various diseases. OBJECTIVE: This study was designed to explore the pharmacokinetic and pharmacodynamic properties of rhubarb anthraquinones extract in diabetic nephropathy and acute liver injury rats. METHODS: The diabetic nephropathy and acute liver injury rats were induced by intraperitoneal injection with streptozotocin (STZ) and carbon tetrachloride (CCL4), respectively. The rats were treated with different doses of rhubarb anthraquinones extract (37.5, 75 and 150mg/kg) as administration groups. For pharmacokinetics, the drug concentrations of rhubarb anthraquinones consisting of rhein, emodin, aloe-emodin, chrysophanol, physcion and sennoside A were determined. For pharmacodynamics, the anti-diabetic nephropathy and hepatoprotective effects were assessed under different dosage regimens. RESULTS: The rhein, emodin, aloe-emodin, chrysophanol were considered as pharmacokinetic markers at three doses of rhubarb anthraquinones extract. In diabetic nephropathy rats, no obvious pharmacokinetic change of the four ingredients was observed compared with control rats. However, the plasma exposures of the four ingredients increased in acute liver injury rats compared with control rats. The serum creatinine (SCr), blood urea nitrogen (BUN) and urine protein (UP) values in diabetic nephropathy rats decreased compared with those in the model group, which suggested that rhubarb anthraquinones extract displayed certain therapeutic and preventive effects against the diabetic nephropathy. However, rhubarb anthraquinones extract cannot ameliorate the CCL4-induced liver injury under the three different dosage regimens. CONCLUSION: There was no significant pharmacokinetic difference after a single oral administration of rhubarb anthraquinones extract between control and diabetic nephropathy rats. However, apparent pharmacokinetic differences were observed between control and liver injury rats. Also, rhubarb anthraquinones extract had beneficial effects on diabetic nephropathy rats, while no marked effect on liver injury rats under the same dosage regimens. SN - 1950-6007 UR - https://www.unboundmedicine.com/medline/citation/28475921/Pharmacokinetics_and_pharmacodynamics_of_rhubarb_anthraquinones_extract_in_normal_and_disease_rats_ DB - PRIME DP - Unbound Medicine ER -