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在小鼠体内长效、高浓度丁丙诺啡溶液的药代动力学和疗效。

Pharmacokinetics and Efficacy of a Long-lasting, Highly Concentrated Buprenorphine Solution in Mice.

机构信息

Laboratory Animal Resources, Office of the Vice President for Research, Colorado State University, Fort Collins, Colorado;, Email:

Laboratory Animal Resources, Office of the Vice President for Research, Colorado State University, Fort Collins, Colorado.

出版信息

J Am Assoc Lab Anim Sci. 2021 Jan 1;60(1):64-71. doi: 10.30802/AALAS-JAALAS-20-000049. Epub 2020 Sep 29.

Abstract

Buprenorphine is a commonly used opioid for mitigating pain in laboratory mice after surgical procedures; however, the dosing interval necessary for standard buprenorphine may require treatment every 4 to 6 h to maintain an adequate plane of analgesia. An alternative formulation that provides prolonged plasma concentration with long-lasting effects would be beneficial in achieving steady-state analgesia. We evaluated a long-lasting and highly concentrated formulation of buprenorphine (Bup-LHC) in mice. Pharmacokinetic analysis was performed to assess plasma concentrations in male C57BL/6J (B6) and female CD1 mice after subcutaneous injection of 0.9 mg/kg. The Bup-LHC formulation provided plasma drug levels that exceeded the therapeutic level for at least 12 h in male B6 mice and was below therapeutic levels by 8 h in female CD1 mice. An experimental laparotomy model was used to assess analgesic efficacy. Female CD1 mice were treated with either Bup-LHC (0.9 mg/kg) or saline at 1 h before undergoing an ovariectomy via a ventral laparotomy. At 3, 6, 12, 24, and 48 h after surgery, pain was assessed based on the following behaviors: orbital tightness, grooming, wound licking, rearing, arched posture, ataxia, piloerection, nest building, and general activity. At 3 and 6 h after surgery, Bup-LHC-treated mice had significantly less wound licking and orbital tightness and considerably higher activity levels than did saline-treated mice. At 12 h, wound licking, orbital tightness and activity in Bup-LHC-treated mice were no longer significantly different from those of saline-treated mice. The results of this study suggest that Bup-LHC at 0.9 mg/kg provides sufficient plasma concentrations for analgesia in mice for 6 to 12 h after administration, as demonstrated behaviorally for at least 6 h after surgery.

摘要

丁丙诺啡是一种常用于减轻手术后实验室小鼠疼痛的阿片类药物;然而,标准丁丙诺啡的给药间隔可能需要每 4 到 6 小时治疗一次,以维持足够的镇痛水平。一种提供延长的血浆浓度和持久效果的替代制剂将有利于实现稳定的镇痛状态。我们评估了丁丙诺啡的一种长效和高浓度制剂(Bup-LHC)在小鼠中的效果。进行了药代动力学分析,以评估皮下注射 0.9mg/kg 后雄性 C57BL/6J(B6)和雌性 CD1 小鼠的血浆浓度。Bup-LHC 制剂在雄性 B6 小鼠中提供的血浆药物水平至少超过治疗水平 12 小时,而在雌性 CD1 小鼠中则在 8 小时内低于治疗水平。使用实验性剖腹手术模型评估镇痛效果。雌性 CD1 小鼠在接受经腹剖腹卵巢切除术之前 1 小时接受 Bup-LHC(0.9mg/kg)或生理盐水治疗。手术后 3、6、12、24 和 48 小时,根据以下行为评估疼痛:眼眶紧闭、梳理、舔伤口、站立、拱形姿势、共济失调、毛发竖起、筑巢和一般活动。手术后 3 和 6 小时,Bup-LHC 治疗的小鼠舔伤口和眼眶紧闭的次数明显减少,活动水平明显高于生理盐水治疗的小鼠。在 12 小时时,Bup-LHC 治疗的小鼠舔伤口、眼眶紧闭和活动水平与生理盐水治疗的小鼠不再有显著差异。这项研究的结果表明,Bup-LHC 在 0.9mg/kg 时在给药后 6 至 12 小时内为小鼠提供了足够的血浆浓度用于镇痛,至少在手术后 6 小时内通过行为学得到证实。

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