the endothelin system has an important role in bone modelling during orthodontic tooth movement (otM); however, little is known about the involvement of endothelin B receptors (et B) in this process. the aim of this study was to evaluate the role of et B in bone modelling during otM using et B knockout rats (et B-KO). Thirty-two male rats were divided into 4 groups (n = 8 per group): the ET B-Ko appliance group, et B-Ko control group, wild type (et B-Wt) appliance group, and et B-Wt control group. the appliance consisted of a super-elastic closed-coil spring placed between the first and second left maxillary molar and the incisors. Tooth movement was measured on days 0 and 35, and maxillary alveolar bone volume, osteoblast, and osteoclast volume were determined histomorphometrically on day 35 of OTM. Next, we determined the serum endothelin 1 (ET-1) level and gene expression levels of the osteoclast activity marker cathepsin K and osteoblast activity markers osteocalcin and dentin matrix acidic phosphoprotein 1 (DMP1) on day 35. The ET B-KO appliance group showed significantly lower osteoblast activity, diminished alveolar bone volume and less otM than the et B-Wt appliance group. our results showed that et B is involved in bone modelling in the late stage of otM. Endothelin 1 (ET-1) plays an important role in the regulation of bone metabolism in physiological as well as in pathophysiological processes 1-4. It has a known role in the maintenance of bone homeostasis and the regulation of osteoblastic function. ET-1 stimulates the proliferation, differentiation and activity of osteoblasts 5,6 and inhibits osteoblast apoptosis, promoting osteoblastic growth 7. ET-1 acts through both endothelin A (ET A) and endothelin B (ET B) receptors. Specifically, it has been shown that the ET-1/ET A axis is an important regulator of osteoblast activity; targeted inactivation of ET A in mature osteoblasts induced lower tibial trabecular bone volume in vivo 8. However, less is known about the role of ET B in osteogenesis. In one study, treatment with the dual ET A and ET B antagonist Macitentan showed decreased vertebral bone mass in mice, potentially from decreased osteoblast activity as well as from the increased osteoclast activity 9. Several studies also indicate the involvement of endothelins during orthodontic tooth movement (OTM) 10-12. Orthodontic movement is a consequence of applying a force to the teeth. It is a mechanism that involves the biomechanical adaptation of the alveolar process and supporting periodontium. Alterations in the vascularity within the periodontal ligament (PDL), the connective tissue that connects a tooth to its surrounding alveolar bone, may trigger responses at the cellular level, such as alveolar bone modelling 13,14. During OTM areas of pressure and tension are formed in the PDL. At pressure areas, which appear in the direction of the application of force,