Paclitaxel inhibits post-traumatic recurrent laryngeal nerve regeneration into the posterior cricoarytenoid muscle in a canine model.
Paclitaxel inhibits post-traumatic recurrent laryngeal nerve regeneration into the posterior cricoarytenoid muscle in a canine model.
复制标题
在犬模型中,紫杉醇抑制创伤后喉返神经再生为后环杓肌。
DOI:
10.1002/lary.26058
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发表时间:
2017
期刊:
影响因子:
--
通讯作者:
Paniello,RandalC
中科院分区:
文献类型:
--
作者:
Park,AndreaM;Bhatt,NeelK;Paniello,RandalC
Objectives/HypothesisTo investigate the efficacy of paclitaxel, a potent microtubule inhibitor with a more favorable therapeutic index as compared with vincristine, in preventing post‐traumatic nerve regeneration of the recurrent laryngeal nerve into the posterior cricoarytenoid muscle in a canine laryngeal model.Study DesignExperimental animal study.MethodsForty‐nine canine hemilaryngeal specimens were divided into five experimental groups. Under general anesthesia, a tracheostomy, recurrent laryngeal nerve (RLN) transection and repair, and laryngeal adductory pressures (LAP) were measured pre–RLN injury. The approach to the posterior cricoarytenoid (PCA) muscle for neurotoxin injection was transoral or open transcervical, at 0 or 3 months. At 6 months, postinjury LAPs were measured and the animals were sacrificed at 6 months to allow for laryngeal harvesting and analysis.ResultsPaclitaxel demonstrated increased mean laryngeal adductory pressures (70.6%) as compared with saline control (55.5%). The effect of paclitaxel was the same as observed with vincristine at 0 months and with a delayed injection at 3 months. There was no difference between transoral or open injection groups.ConclusionsPCA muscle injection with paclitaxel resulted in improved strength of laryngeal adduction. This effect was similar to that of vincristine at both 0 and 3 months following nerve injury. A single intramuscular injection of paclitaxel was well tolerated. Additional human studies are needed to determine the degree of clinical benefit of this intervention.Level of EvidenceNALaryngoscope, 127:651–655, 2017
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DOI:
10.1111/j.1749-6632.1982.tb22124.x
发表时间:
1982-01-01
影响因子:
5.2
作者:
KUSHNER, I
通讯作者:
KUSHNER, I
DOI:
10.1073/pnas.84.23.8619
发表时间:
1987
影响因子:
11.1
作者:
Warren,RS;Donner,DB;StarnesJr,HF;Brennan,MF
通讯作者:
Brennan,MF
DOI:
10.1152/ajpendo.1984.247.3.e405
发表时间:
1984
期刊:
The American journal of physiology
影响因子:
--
作者:
Carpentier,YA;Jeevanandam,M;Robin,AP;Nordenstrom,J;Burr,RE;Leibel,RL;Hirsch,J;Elwyn,DH;Kinney,JM
通讯作者:
Kinney,JM
影响因子:
15.9
作者:
SIMMONS, PS;MILES, JM;HAYMOND, MW
通讯作者:
HAYMOND, MW
DOI:
10.1001/archsurg.1987.01400240042007
发表时间:
1987
期刊:
Archives of surgery (Chicago, Ill. : 1960)
影响因子:
--
作者:
Warren,RS;StarnesJr,HF;Gabrilove,JL;Oettgen,HF;Brennan,MF
通讯作者:
Brennan,MF