TY - JOUR
T1 - NGF prevention of neurotoxicity induced by cisplatin, vincristine and taxol depends on toxicity of each drug and NGF treatment schedule
T2 - In vitro study of adult rat sympathetic ganglion explants
AU - Hayakawa, Kazuhiro
AU - Itoh, Takayuki
AU - Niwa, Hisayoshi
AU - Mutoh, Tatsuro
AU - Sobue, Gen
N1 - Funding Information:
We thank Dr. Shigeki Sawada, Mr. Taneo Fukuta, Dr. Satoru Hosokawa, Dr. Jun-ichi Nakanowatari and Dr. Fumio Sagami for their helpful advice, and Mr. Nobuhiro Hibino, Eisai, for technical assistance. A part of this study was supported by grants from the Ministry of Health and Welfare of Japan, and from the Uehara Memorial Research Foundation.
Copyright:
Copyright 2007 Elsevier B.V., All rights reserved.
PY - 1998/6/1
Y1 - 1998/6/1
N2 - The simultaneous administration of nerve growth factor (NGF) has been found to prevent experimental neuropathies induced by anti-cancer drugs such as cisplatin, vincristine and taxol. However, it is clinically important to know whether NGF is beneficial once the neuropathy is already manifest. We established a bioassay system to examine the preventive effects of NGF in various treatment schedules. NGF significantly prevented the inhibition of neurite outgrowth by vincristine and taxol regardless of treatment schedules. The pre-treatment and co-treatment schedules were effective against cisplatin, but the post-treatment schedule was not. With regard to the neurite and nerve cell population densities, only the cisplatin group treated with NGF showed lower values than the control. These results indicate that NGF-treatment is effective for the toxic sympathetic nerve injury induced by vincristine and taxol regardless of the treatment schedule, but is not protective against cisplatin-induced nerve cell injury.
AB - The simultaneous administration of nerve growth factor (NGF) has been found to prevent experimental neuropathies induced by anti-cancer drugs such as cisplatin, vincristine and taxol. However, it is clinically important to know whether NGF is beneficial once the neuropathy is already manifest. We established a bioassay system to examine the preventive effects of NGF in various treatment schedules. NGF significantly prevented the inhibition of neurite outgrowth by vincristine and taxol regardless of treatment schedules. The pre-treatment and co-treatment schedules were effective against cisplatin, but the post-treatment schedule was not. With regard to the neurite and nerve cell population densities, only the cisplatin group treated with NGF showed lower values than the control. These results indicate that NGF-treatment is effective for the toxic sympathetic nerve injury induced by vincristine and taxol regardless of the treatment schedule, but is not protective against cisplatin-induced nerve cell injury.
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U2 - 10.1016/S0006-8993(98)00305-9
DO - 10.1016/S0006-8993(98)00305-9
M3 - Article
C2 - 9622663
AN - SCOPUS:0032102171
SN - 0006-8993
VL - 794
SP - 313
EP - 319
JO - Brain Research
JF - Brain Research
IS - 2
ER -