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A pilot study of dental pharmacotherapy for alveolar bone regeneration 牙槽骨再生的牙科药物治疗的初步研究
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2017-01-01 DOI: 10.11263/JSOTP.17.13
M. Kawai, M. Kawai, Fumihiko Kohno, M. Sakumoto, Ayumi Taeda, N. Shiotsu, Toshio Yamamoto, K. Ohura
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引用次数: 0
Mucogingival surgery: where we stand today. 黏膜龈手术:我们的现状。
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2011-08-01 DOI: 10.1080/19424396.2011.12221930
Vivek K Bains, Vivek Gupta, G P Singh, Rhythm Bains

Mucogingival problems are developmental and acquired aberrations in the morphology, position, and/or the amount of gingiva surrounding teeth. According to an academic report by American Academy of Periodontology, mucogingival therapy should be advocated for gingival augmentation and to create adequate vestibular depth in areas with insufficient attached gingiva. This paper provides an overview on mucogingival surgical procedures from its inception to the current time.

黏膜龈问题是牙齿周围牙龈的形态、位置和/或数量的发育和后天畸变。根据美国牙周病学会的一份学术报告,黏膜龈治疗应提倡用于牙龈增量,并在附着龈不足的区域创造足够的前庭深度。本文概述了粘龈手术从开始到现在的发展过程。
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引用次数: 0
Triacylated lipopeptide, a component of Gram-positive bacteria, induces osteoclastogenesis in the absence of RANKL and resorbs calvarial bone in vivo through Toll-like receptor 2 三酰化脂肽是革兰氏阳性菌的一种成分,在缺乏RANKL的情况下诱导破骨细胞发生,并通过toll样受体2在体内吸收颅骨骨
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2010-04-01 DOI: 10.11263/JSOTP.29.9
Keiko Suzuki, S. Yamada
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引用次数: 2
Analysis of the stability and microbiological safety of aznol saline gargle in hospital preparations widely used for the treatment of oral cancer patients with oral mucositis 广泛用于治疗口腔癌合并口腔黏膜炎患者的医院制剂中氮盐含漱液的稳定性和微生物安全性分析
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2008-12-01 DOI: 10.11263/JSOTP1982.27.143
M. Ushiyama, R. Ikeda, T. Nitta, Yusuke Tazitsu, A. Miyawaki, Tatsuya Yamaguchi, Y. Shimodouzono, K. Ushinohama, R. Matsui, K. Sugihara, N. Nakamura, Katsushi Yamada
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引用次数: 1
Results of medicine revaluation in the odontology department 齿科药物重估结果分析
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2008-12-01 DOI: 10.11263/JSOTP1982.27.151
Yoshio Saito
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引用次数: 0
A possible therapeutic for gingival overgrowth caused by calcium channel blockers 一种治疗钙通道阻滞剂引起的牙龈过度生长的可能方法
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2008-08-01 DOI: 10.11263/JSOTP1982.27.103
H. Matsumoto, R. Takeuchi, M. Ono, Y. Akimoto, A. Fujii
In the present study, the results of characters in nifedipine responders (NIFr) and nifedipine non-responders (NIFn) are summarized, and the possibility of using tenidap and 18ƒ¿ -glycyrrhetinic acid (18ƒ¿-GA) as a therapeutic for gingival overgrowth caused by calcium channel blockers is investigated. 18ƒ¿-GA inhibited cell proliferation and G1/S transition were induced in NIFr cells. It was also shown that cell cycle control proteins were down-stream targets in the growth-inhibition activity of 18ƒ¿-GA in NIFr cells. Tenidap discharges intracellular Ca2+ store, resulting in a depletion of intracellular Ca2+ store in NIFr cells. It also inhibits cell growth, DNA and collagen syntheses, lowered intracellular pH, and enhanced matrix metalloproteinase-1 formation in NIFr cells. These results suggest that 18ƒ¿-GA and tenidap might be effective for the prevention of gingival overgrowth caused by calcium channel blockers.
本研究总结硝苯地平应答者(NIFr)和硝苯地平无应答者(NIFn)的特征,并探讨了使用tenidap和18f¿-甘草次酸(18f¿-GA)治疗钙通道阻滞剂引起的牙龈过度生长的可能性。18f¿-GA抑制NIFr细胞增殖,诱导G1/S转变。在NIFr细胞中,细胞周期控制蛋白是18f¿-GA生长抑制活性的下游靶点。Tenidap释放细胞内Ca2+储存,导致NIFr细胞内Ca2+储存的消耗。它还抑制细胞生长,DNA和胶原合成,降低细胞内pH值,并增强NIFr细胞中基质金属蛋白酶-1的形成。上述结果提示,18f¿-GA和tenidap可有效预防钙通道阻滞剂引起的牙龈过度生长。
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引用次数: 0
A randomized controlled trial comparison between ropivacaine and 2% lidocaine containing adrenalin for inferior alveolar nerve block during implant surgery 一项随机对照试验比较罗哌卡因和2%利多卡因含肾上腺素在种植手术中用于下牙槽神经阻滞
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2008-08-01 DOI: 10.11263/JSOTP1982.27.125
S. Ogura, K. Shinohara, Katsuhisa Sunada, H. Takamori, Kiminari Nakamura
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引用次数: 1
Study on the mechanism of collagen metabolism in phenytoin-induced gingival overgrowth 苯妥英诱导牙龈过度生长中胶原代谢机制的研究
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2008-08-01 DOI: 10.11263/JSOTP1982.27.86
Takahiro Kato
Gingival overgrowth is a serious adverse effect associated with the administration of phenytoin (PHT), with PHT-induced gingival overgrowth characterized by a massive accumulation of extracellular matrix components, especially collagen, in gingival connective tissues. However, the etiology of such collagen accumulation is still largely unknown. We examined the effects of PHT on the collagen degradation process leading to collagen accumulation in human gingival fibroblasts (HGF). PHT causes an impaired degradation of collagen by suppression of enzymatic degradation with MMPs/TIMP-1 and ƒ¿2 ƒÀ1 integrin mediated endocytosis. These synergistic effects may cause collagen accumulation, leading to gingival overgrowth. It has also been reported that dental plaque is the most important factor to enhance deterioration caused by PHT-induced
牙龈过度生长是与苯妥英(PHT)相关的严重不良反应,PHT诱导的牙龈过度生长以牙龈结缔组织中细胞外基质成分(尤其是胶原)的大量积累为特征。然而,这种胶原堆积的病因在很大程度上仍然是未知的。我们研究了PHT对导致人牙龈成纤维细胞(HGF)胶原积累的胶原降解过程的影响。PHT通过抑制MMPs/TIMP-1和整合素介导的内吞作用来抑制酶降解,从而导致胶原降解受损。这些协同作用可能导致胶原蛋白积聚,导致牙龈过度生长。也有报道称牙菌斑是促进pht引起的恶化的最重要因素
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引用次数: 0
Current status of treatment modalities for drug-induced gingival overgrowth 药物性牙龈过度生长的治疗现状
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2008-08-01 DOI: 10.11263/JSOTP1982.27.68
Koichi Ito
Gingival hyperplasia (overgrowth) is a well-documented unwanted effect, associated with phenytoin, the calcium channel blockers, and cyclosporin. The pathogenesis of drug-induced gingival hyperplasia is uncertain. However, the identification of risk factors associated with both the prevalence and severity of drug-induced gingival hyperplasia is important for all parties involved with this unwanted effect. Prevalence of gingival hyperplasia with phenytoin, the calcium channel blockers, and cyclosporin is approximately 50%, 10-20%, and 8-70%, respectively. The inflammatory components of drug-induced gingival hyperplasia can be managed effectively for the majority of patients with a plaque control program and nonsurgical periodontal therapy including oral hygiene instruction, scaling and root planing coupled with continued periodontal maintenance procedures. After reevaluation, some patients may need surgical periodontal therapy and maintenance procedures. Maintenance therapy including appropriate oral home care appear to be effective in controlling the drug-induced gingival hyperplasia and in maintaining clinical improvements for a long time.
牙龈增生(过度生长)是一种有充分证据的不良影响,与苯妥英、钙通道阻滞剂和环孢素有关。药物性牙龈增生的发病机制尚不明确。然而,确定与药物性牙龈增生的患病率和严重程度相关的危险因素对所有涉及这种不良影响的各方都很重要。苯妥英、钙通道阻滞剂和环孢素牙龈增生的患病率分别约为50%、10-20%和8-70%。对于大多数患者来说,通过菌斑控制计划和非手术牙周治疗,包括口腔卫生指导、洗牙和牙根规划以及持续的牙周维护程序,可以有效地控制药物引起的牙龈增生的炎症成分。在重新评估后,一些患者可能需要手术牙周治疗和维持程序。包括适当的口腔家庭护理在内的维持治疗在控制药物性牙龈增生和长期保持临床改善方面是有效的。
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引用次数: 0
Medical lawsuits judged by using drug package inserts as criteria for the judicial decisions 以药品说明书为裁判标准的医疗诉讼
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2008-08-01 DOI: 10.11263/JSOTP1982.27.116
Yohko Kaku, K. Enami, M. Fukumoto, M. Yamaguchi, K. Shibutani
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引用次数: 1
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Oral Therapeutics and Pharmacology
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