Bone protection effects of a novel Chinese herbal formula, taikong yangxin prescription, in hindlimb unloaded rats against bone deterioration.
- Author:
Chun-hay KO
1
;
Wing-sum SIU
1
;
Chung-lap CHAN
1
;
Chi-man KOON
1
;
Kwok-pui FUNG
1
;
Yong-zhi LI
2
;
Ying-hui LI
2
;
Ping-chung LEUNG
3
Author Information
- Publication Type:Journal Article
- Keywords: Chinese herbal medicine; micro-computerized tomography; osteoporosis peripheral quantitative computed tomography; tail-suspension rat model
- MeSH: Animals; Biomechanical Phenomena; drug effects; Bone Density; drug effects; Bone and Bones; diagnostic imaging; drug effects; Drugs, Chinese Herbal; administration & dosage; pharmacology; Femur; Male; Rats; Rats, Sprague-Dawley; Tibia; Tomography Scanners, X-Ray Computed; Weightlessness; X-Ray Microtomography
- From: Chinese journal of integrative medicine 2015;21(10):759-764
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo investigate the protective effects of a Chinese herbal formula, taikong yangxin prescription (TKYXP) against bone deterioration in a hindlimb unloaded (tail-suspension) rat model.
METHODSThirty-two male Sprague-Dawley rats were divided into 4 groups: tail-suspension group fed with 2.5 g•kg(-1)•day(-1) of TKYXP extract (high dose), tail-suspension group fed with 1.25 g•kg(-1)•day(-1) (low dose), tail-suspended group treated with water placebo (placebo control group) and non tail-suspended group. The effects of TKYXP on bone were assessed using peripheral quantitative computed tomography (pQCT), microcomputerized tomography (micro-CT) and three-point bending biomechanical test on the femur in vivo.
RESULTSTKYXP had a significant protective effect against bone loss induced by tail-suspension on day 28, as shown in the reduction in bone mineral density (BMD) loss, preservation of bone micro-architecture and biomechanical strength. The administration ofhigh dose TKYXP could significantly reduce the total BMD loss by 4.8% and 8.0% at the femur and tibia regions, respectively, compared with the placebo control group (P<0.01) on day 28. Its bone protective effect on the femur was further substantiated by the increases of the trabecular BMD (by 6.6%), bone volume fraction (by 20.9%), trabecular number (by 9.5%) and thickness (by 11.9%) as compared with the placebo control group.
CONCLUSIONTKYXP may protect the bone under weightless influence from gradual structural deterioration in the tail-suspension model.