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Estudio2019

Effect of caffeine on ovariectomy-induced osteoporosis in rats

Xu H, Liu T, Hu L, Li J, Gan C, Xu J, Chen F, Xiang Z, Wang X, Sheng J

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 40 citas

Cómo se estudió

Diseño
Estudio en animales (clasificado por nuestro filtro de IA)
Estudiado en
Animales
Resultado principal
Marcadores de salud y funcionamiento

Quién lo pagó

Financiación
Financiación independiente
Gobierno
Major Scientific and Technological Special Project of Yunnan Province
Gobierno
Young Academic and Technological Leaders of Yunnan Province
Universidad u hospital
Academic Leaders of Yunnan Province

Según 3 financiadores declarados.

Publicación

Publicado
2019-02-21 · Biomed Pharmacother · vol. 112 · pág. 108650
Editorial
Elsevier BV
Citado
67 citas · más que el 91% de estudios similares · 2.5× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
52 trabajos
Acceso
Acceso abierto (revista) · CC-BY-NC-ND
Áreas de investigación
Bone health and treatments · Bone health and osteoporosis research · Cancer Risks and Factors
Palabras clave
Ovariectomized rat, Caffeine, Endocrinology, Internal medicine, Osteoporosis, Raloxifene, Alkaloid, Xanthine, Calcium, Medicine, Bone mineral, In vivo, Chemistry, Estrogen, Biology, Estrogen receptor, Biochemistry
MeSH
animals, humans, rats, rats, wistar, osteoporosis, postmenopausal, caffeine, phosphodiesterase inhibitors, organ size, ovariectomy, bone density, dose-response relationship, drug, female, lipid metabolism

10 autores

  • Huanhuan Xu🇨🇳Yunnan Agricultural University; Tea Research Institute
  • Titi Liu🇨🇳Yunnan Agricultural University; Tea Research Institute
  • Lihong Hu🇨🇳Yunnan Agricultural University; Tea Research Institute
  • Li Jin🇨🇳Yunnan Agricultural University; Tea Research Institute
  • Chunxia Gan🇨🇳Yunnan Agricultural University; Tea Research Institute
  • Jing Xu🇨🇳Yunnan Agricultural University; Tea Research Institute
  • Fei Chen🇨🇳Yunnan Agricultural University; Tea Research Institute
  • Zemin Xiang🇨🇳 · autor de correspondenciaYunnan Agricultural University; Tea Research Institute
  • Xuanjun Wang🇨🇳 · autor de correspondenciaYunnan Agricultural University; Tea Research Institute
  • Jun Sheng🇨🇳 · autor de correspondenciaYunnan Agricultural University; Tea Research Institute

Resumen

El texto original del estudio, en el idioma en que se publicó.

Caffeine (1,3,7-trimethylxanthine) is a naturally occurring plant xanthine alkaloid present in many commonly consumed beverages worldwide, including tea, coffee, and cocoa. Although moderate caffeine intake is generally considered to exert positive effects on human health, its effect on bone metabolism remains controversial. The aim of this study was to systematically evaluate the pharmacological effect of long-term administration of caffeine on ovariectomy-induced postmenopausal osteoporosis in female rats. A sham operation or ovariectomy was performed to establish the ovariectomy rat model. The ovariectomized (OVX) rats were divided into five subgroups: OVX with vehicle (model), OVX with raloxifene hydrochloride (RLX, positive control; 4 mg/kg body weight/day), and OVX with low-, medium-, and high-dose caffeine (9.6, 19.2, and 38.4 mg/kg of body weight/day, respectively). Their corresponding treatments were administered intragastrically for 13 weeks. In-vivo studies showed that treatment with caffeine effectively improved the lipid profiles and increased the concentration of calcium in the serum of OVX rats. Medium- or high-dose treatment with caffeine significantly decreased the activities of alkaline and acid phosphatases in OVX rats. In addition, treatment with caffeine (at any dose) did not adversely affect organ weights, organ coefficients, femoral length, bone mineral density, biomechanical properties, or bone microarchitecture in OVX rats. Collectively, our study demonstrated that caffeine did not exert a damaging effect on the skeletal system of OVX rats.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial (CC BY-NC-ND).

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