Duarte Poliana M, Miranda Tamires S, Marins Letícia M, Perez Erick G, Copes Liliana G, Tonietto Cristine B, Montalli Victor A M, Malta Fernando S, Napimoga Marcelo H
Department of Periodontology, Dental Research Division, UNG - Universidade Guarulhos, Guarulhos, SP, Brazil.
Department of Periodontology, College of Dentistry, University of Florida, Gainesville, FL, USA.
Braz Dent J. 2020 Nov-Dec;31(6):640-649. doi: 10.1590/0103-6440202003595.
The purpose of this investigation was to evaluate the effects of lithium chloride (LiCl) on the socket healing of estrogen-deficient rats. Seventy-two rats were allocated into one of the following groups: Control, Ovariectomy and LiCl (150 mg/kg/2 every other day orally) + Ovariectomy. Animals received LiCl or water from the 14th day post-ovariectomy, until the completion of the experiment. On the 21st day after ovariectomy, the first molars were extracted. Rats were euthanized on the 10th, 20th and 30th days following extractions. Bone healing (BH), TRAP positive cells and immunohistochemical staining for OPG, RANKL, BSP, OPN and OCN were evaluated. The Ovariectomy group presented decreased BH compared to the LiCl group at 10 days, and the lowest BH at 20 days (p<0.05). At 30 days, the Ovariectomy and LiCl-groups presented lower BH than that of the Control (p<0.05). The number of TRAP-stained cells was the lowest in the LiCl group at 20 days and the highest in the Ovariectomy group at 30 days (p<0.05). At 10 days of healing, the LiCl group demonstrated stronger staining for all bone markers when compared to the other groups, while the Ovariectomy group presented higher RANKL expression than that of the Control (p<0.05). LiCl enhanced bone healing in rats with estrogen deficiency, particularly in the initial healing phases. However, as data on the effects of lithium chloride on bone tissue are still preliminary, more studies related to its toxicity and protocol of administration are necessary before its application in clinical practice.
本研究的目的是评估氯化锂(LiCl)对雌激素缺乏大鼠牙槽窝愈合的影响。72只大鼠被分为以下几组之一:对照组、卵巢切除组和LiCl(150 mg/kg/每隔一天口服)+卵巢切除组。动物在卵巢切除术后第14天开始接受LiCl或水,直至实验结束。在卵巢切除术后第21天,拔除第一磨牙。在拔牙后的第10、20和30天对大鼠实施安乐死。评估骨愈合(BH)、抗酒石酸酸性磷酸酶(TRAP)阳性细胞以及骨保护素(OPG)、核因子κB受体活化因子配体(RANKL)、骨涎蛋白(BSP)、骨桥蛋白(OPN)和骨钙素(OCN)的免疫组织化学染色情况。卵巢切除组在10天时的骨愈合情况比LiCl组差,在20天时骨愈合程度最低(p<0.05)。在30天时,卵巢切除组和LiCl组的骨愈合程度均低于对照组(p<0.05)。TRAP染色细胞数量在LiCl组20天时最少,在卵巢切除组30天时最多(p<0.05)。在愈合10天时,LiCl组与其他组相比,所有骨标志物的染色更强,而卵巢切除组的RANKL表达高于对照组(p<0.05)。LiCl可促进雌激素缺乏大鼠的骨愈合,尤其是在愈合初期。然而,由于关于氯化锂对骨组织影响的数据仍处于初步阶段,在临床实践中应用之前,有必要进行更多关于其毒性和给药方案的研究。