PURPOSE: The aim of this study was to explore the effects of various bone grafting substitutes (Osteosponge, Perioglas, Tutoplast, and Surgibone) on vascular smooth muscle tonus. METHODS: Bilateral carotid arteries were removed from rats and contraction/relaxation of isolated vessel rings were measured before and after contact with the biomaterials and then, for dose-dependent epinephrine and papaverin administrations, by a force displacement transducer. The data of each biomaterial group were collected by a computerized system and corresponding software at a sample rate of 1,000 kHz and were converted to contraction force. RESULTS: Vascular contraction forces were influenced in response to biomaterials tested except for Osteosponge (P < 0.05), although the differences between groups were insignificant (P > 0.05). There was a dose-dependent vascular response to epinephrine and papaverine administration upon biomaterial contact (P < 0.05). The dose-dependent vascular responses to epinephrine and papaverine administration were almost similar for all biomaterials tested (P < 0.05), suggesting that the biomaterials led to reversible effects on vascular contraction/relaxation behavior, which resulted in recovery. CONCLUSIONS: Osteosponge, Perioglas, Tutoplast, and Surgibone do not alter vascular smooth muscle tonus and vitality and therefore would, presumably, not jeopardize the angiogenesis of fresh blood vessels and full vascularization during tissue healing.
PURPOSE: The aim of this study was to explore the effects of various bone grafting substitutes (Osteosponge, Perioglas, Tutoplast, and Surgibone) on vascular smooth muscle tonus. METHODS: Bilateral carotid arteries were removed from rats and contraction/relaxation of isolated vessel rings were measured before and after contact with the biomaterials and then, for dose-dependent epinephrine and papaverin administrations, by a force displacement transducer. The data of each biomaterial group were collected by a computerized system and corresponding software at a sample rate of 1,000 kHz and were converted to contraction force. RESULTS: Vascular contraction forces were influenced in response to biomaterials tested except for Osteosponge (P < 0.05), although the differences between groups were insignificant (P > 0.05). There was a dose-dependent vascular response to epinephrine and papaverine administration upon biomaterial contact (P < 0.05). The dose-dependent vascular responses to epinephrine and papaverine administration were almost similar for all biomaterials tested (P < 0.05), suggesting that the biomaterials led to reversible effects on vascular contraction/relaxation behavior, which resulted in recovery. CONCLUSIONS: Osteosponge, Perioglas, Tutoplast, and Surgibone do not alter vascular smooth muscle tonus and vitality and therefore would, presumably, not jeopardize the angiogenesis of fresh blood vessels and full vascularization during tissue healing.
Authors: Jasmin Lienau; Hanna Schell; Georg N Duda; Petra Seebeck; Sarah Muchow; Hermann J Bail Journal: J Orthop Res Date: 2005-05 Impact factor: 3.494
Authors: Flávia A C Furlaneto; Maria J H Nagata; Stephen E Fucini; Tatiana M Deliberador; Tetuo Okamoto; Michel R Messora Journal: Clin Oral Implants Res Date: 2007-02-13 Impact factor: 5.977
Authors: Murat Cavit Cehreli; Mehmet Ali Onur; Zeynep Taş; Saime Sahin Journal: J Biomed Mater Res B Appl Biomater Date: 2004-08-15 Impact factor: 3.368
Authors: Zvi Schwartz; Moshe Goldstein; Einav Raviv; Ariel Hirsch; Don M Ranly; Barbara D Boyan Journal: Clin Oral Implants Res Date: 2007-04 Impact factor: 5.977