Tocotrienol as a Protecting Agent against Glucocorticoid-Induced Osteoporosis: A Mini Review of Potential Mechanisms

Molecules. 2022 Sep 9;27(18):5862. doi: 10.3390/molecules27185862.

Abstract

Glucocorticoid-induced osteogenic dysfunction is the main pathologyical mechanism underlying the development of glucocorticoid-induced osteoporosis. Glucocorticoids promote adipogenic differentiation and osteoblast apoptosis through various pathways. Various ongoing studies are exploring the potential of natural products in preventing glucocorticoid-induced osteoporosis. Preclinical studies have consistently shown the bone protective effects of tocotrienol through its antioxidant and anabolic effects. This review aims to summarise the potential mechanisms of tocotrienol in preventing glucocorticoid-induced osteoporosis based on existing in vivo and in vitro evidence. The current literature showed that tocotrienol prevents oxidative damage on osteoblasts exposed to high levels of glucocorticoids. Tocotrienol reduces lipid peroxidation and increases oxidative stress enzyme activities. The reduction in oxidative stress protects the osteoblasts and preserves the bone microstructure and biomechanical strength of glucocorticoid-treated animals. In other animal models, tocotrienol has been shown to activate the Wnt/β-catenin pathway and lower the RANKL/OPG ratio, which are the targets of glucocorticoids. In conclusion, tocotrienol enhances osteogenic differentiation and bone formation in glucocorticoid-treated osteoblasts while improving structural integrity in glucocorticoid-treated rats. This is achieved by preventing oxidative stress and osteoblast apoptosis. However, these preclinical results should be validated in a randomised controlled trial.

Keywords: anti-inflammatory; antioxidant; bone; osteoblasts; osteoporosis; steroids.

Publication types

  • Review

MeSH terms

  • Anabolic Agents* / pharmacology
  • Animals
  • Antioxidants / metabolism
  • Biological Products* / pharmacology
  • Glucocorticoids / adverse effects
  • Osteoblasts
  • Osteogenesis
  • Osteoporosis* / chemically induced
  • Osteoporosis* / drug therapy
  • Osteoporosis* / metabolism
  • Rats
  • Tocotrienols* / chemistry
  • Tocotrienols* / pharmacology
  • beta Catenin / metabolism

Substances

  • Anabolic Agents
  • Antioxidants
  • Biological Products
  • Glucocorticoids
  • Tocotrienols
  • beta Catenin