Intrathecal pramoxine causes long-lasting spinal sensory and motor block in rats

Author:

Chou An-Kuo12,Chiu Chong-Chi34,Han Ming-Ming5,Chen Yu-Wen67,Wang Jhi-Joung6,Hung Ching-Hsia89ORCID

Affiliation:

1. Department of Anesthesiology, China Medical University Hospital, Taichung, Taiwan

2. School of Medicine, College of Medicine, China Medical University, Taichung, Taiwan

3. Department of General Surgery, Chi Mei Medical Center, Tainan and Liouying, Taiwan

4. Department of Electrical Engineering, Southern Taiwan University of Science and Technology, Tainan, Taiwan

5. Department of Anesthesiology, Anhui Provincial Hospital, Anhui Medical University, Hefei, China

6. Department of Medical Research, Chi-Mei Medical Center, Tainan, Taiwan

7. Department of Physical Therapy, College of Health Care, China Medical University, Taichung, Taiwan

8. Department of Physical Therapy, College of Medicine, National Cheng Kung University, Tainan, Taiwan

9. Institute of Allied Health Sciences, College of Medicine, National Cheng Kung University, Tainan, Taiwan

Abstract

Abstract Objectives The objective of this experiment was to investigate spinal anaesthetic effects of pramoxine and its comparison with bupivacaine, a long-lasting local anaesthetic. Methods After intrathecal injection, three neurobehavioural assessments, which consisted of nociceptive, proprioceptive and motor block, were constructed in rats. The effects of bupivacaine and pramoxine (four doses of each drug) in a dose-related manner were conducted to obtain the ED50 (50% effective dose). Pramoxine potency and duration at provoking spinal nociceptive, proprioceptive and motor block were compared with those of bupivacaine. Key findings We manifested that pramoxine provoked dose-relatedly spinal blockades of nociception, proprioception and motor function. Based on the ED50, the rank potency at producing spinal nociceptive, proprioceptive and motor block was bupivacaine (0.90 (0.82–1.02), 1.00 (0.92–1.08) and 1.16 (1.02–1.34) μmol/kg) greater (P < 0.01 for the differences) than pramoxine (15.47 (14.04–17.05), 16.46 (15.06–17.99), and 17.77 (16.48–19.15) μmol/kg). The spinal block duration created by bupivacaine was not predominantly different (P > 0.05 for the differences) from that created by pramoxine at the equipotent doses (ED75, ED50 and ED25). Conclusions Our preclinical experiment indicated that pramoxine elicited a dose-related spinal block, was less potent than bupivacaine and had a similar duration of spinal block compared with bupivacaine.

Funder

Ministry of Science and Technology in Taiwan

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

Reference36 articles.

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2. The safety of pramoxine hydrochloride when used as a topical (surface) anesthetic;Fisher;Cutis,1998

3. Clinical evaluation of a topical anaesthetic preparation (pramoxine hydrochloride and hydrocortisone) in post-episiotomy pain relief;Hanretty;Br J Clin Pract,1984

4. Local anesthetic activity of pramoxine hydrochloride (tronothane);Blanpin;Anesth Analg (Paris),1957

5. Pharmacology of local anesthetics;Jackson;Ophthalmol Clin North Am,2006

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