Literature DB >> 23302645

Intrathecal ketamine and pregabalin at sub-effective doses synergistically reduces neuropathic pain without motor dysfunction in mice.

Hyung Sun Lim1, Jae-Min Kim, Jae-Gyun Choi, Young Kwon Ko, Yong Sup Shin, Beyong Hwa Jeon, Jin Bong Park, Jang-Hern Lee, Hyun-Woo Kim.   

Abstract

Peripheral or central nerve injury often leads to neuropathic pain. Although ketamine and pregabalin are first line options for the treatment of neuropathic pain, their clinical application is limited due to side effects such as sedation, dizziness and somnolence. We designed this study to determine whether the intrathecal (i.t.) co-treatment with ketamine and pregabalin at sub-effective low doses would elicit a sufficient pain relief without producing side effect in a neuropathic pain mouse model. At day 7 after chronic constriction injury (CCI) of sciatic nerve, dose dependent effects of i.t. ketamine (3, 10, 30, 100 µg) or i.t. pregabalin (10, 30, 100 µg) on mechanical allodynia and thermal hyperalgesia were measured. For combination treatment, 3 or 10 µg of ketamine and 30 µg of pregabalin were selected because these doses of drugs were not effective on neuropathic pain. Interestingly, combined i.t. treatment groups (ketamine 3 µg+pregabalin 30 µg and ketamine 10 µg+pregabalin 30 µg) produced strong analgesia on neuropathic pain although these doses of ketamine and pregabalin alone are not effective. Moreover, rota rod test revealed that normal motor function was not affected by combined treatment while i.t. ketamine at doses above 10 µg showed a significant motor dysfunction. Results of this study suggested that i.t. co-treatment with ketamine and pregabalin at sub-effect low doses may be a useful therapeutic method for the treatment of neuropathic pain patients.

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Year:  2013        PMID: 23302645     DOI: 10.1248/bpb.b12-00760

Source DB:  PubMed          Journal:  Biol Pharm Bull        ISSN: 0918-6158            Impact factor:   2.233


  7 in total

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Authors:  Amitabh Gulati; Vinay Puttanniah; Joseph Hung; Vivek Malhotra
Journal:  Curr Pain Headache Rep       Date:  2014-02

Review 2.  Intrathecal drug delivery for chronic pain management-scope, limitations and future.

Authors:  M Czernicki; G Sinovich; I Mihaylov; B Nejad; S Kunnumpurath; G Kodumudi; N Vadivelu
Journal:  J Clin Monit Comput       Date:  2014-08-31       Impact factor: 2.502

3.  A comparison of intrathecal magnesium and ketamine in attenuating remifentanil-induced hyperalgesia in rats.

Authors:  Jiehao Sun; Hai Lin; Xiaona Feng; Jiaojiao Dong; Emmanuel Ansong; Xuzhong Xu
Journal:  BMC Anesthesiol       Date:  2016-09-06       Impact factor: 2.217

4.  NMDA receptor antagonists attenuate intrathecal morphine-induced pruritus through ERK phosphorylation.

Authors:  Le Shen; Weijia Wang; Siyu Li; Jing Qin; Yuguang Huang
Journal:  Mol Brain       Date:  2018-06-28       Impact factor: 4.041

5.  Deepening the Mechanisms of Visceral Pain Persistence: An Evaluation of the Gut-Spinal Cord Relationship.

Authors:  Elena Lucarini; Carmen Parisio; Jacopo J V Branca; Cristina Segnani; Chiara Ippolito; Carolina Pellegrini; Luca Antonioli; Matteo Fornai; Laura Micheli; Alessandra Pacini; Nunzia Bernardini; Corrado Blandizzi; Carla Ghelardini; Lorenzo Di Cesare Mannelli
Journal:  Cells       Date:  2020-07-24       Impact factor: 6.600

6.  Analgesic effect of recombinant GABAergic precursors releasing ω-conotoxin MVIIA in a model of peripheral nerve injury in rats.

Authors:  Stanislava Jergova; Melissa Hernandez; Jacqueline Sagen
Journal:  Mol Pain       Date:  2022-04       Impact factor: 3.370

7.  Inhibition of glycogen synthase kinase-3β prevents remifentanil-induced hyperalgesia via regulating the expression and function of spinal N-methyl-D-aspartate receptors in vivo and vitro.

Authors:  Yize Li; Haiyun Wang; Keliang Xie; Chunyan Wang; Zhuo Yang; Yonghao Yu; Guolin Wang
Journal:  PLoS One       Date:  2013-10-16       Impact factor: 3.240

  7 in total

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