Thirteen-Week Study of PM014 Subchronic Oral Toxicity in Rats

PM014 is a modified herbal formula based on Chung-Sang-Bo-Ha-Tang, which is a well-known prescription drug used for curing various inflammatory pulmonary diseases. We previously showed that PM014 attenuated lung inflammation in a murine model of chronic obstructive pulmonary disease (COPD). The obje...

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Main Authors: Hwan-Suck Chung, Hyunil Lee, Hyunsu Bae
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:Evidence-Based Complementary and Alternative Medicine
Online Access:http://dx.doi.org/10.1155/2014/189673
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spelling doaj-7505a1eb429a472bbba67249452835f52020-11-24T22:23:15ZengHindawi LimitedEvidence-Based Complementary and Alternative Medicine1741-427X1741-42882014-01-01201410.1155/2014/189673189673Thirteen-Week Study of PM014 Subchronic Oral Toxicity in RatsHwan-Suck Chung0Hyunil Lee1Hyunsu Bae2Department of Physiology, College of Korean Medicine, Kyung Hee University, No. 1 Hoeki-Dong, Dongdaemoon-gu, Seoul 130-701, Republic of KoreaDepartment of Physiology, College of Korean Medicine, Kyung Hee University, No. 1 Hoeki-Dong, Dongdaemoon-gu, Seoul 130-701, Republic of KoreaDepartment of Physiology, College of Korean Medicine, Kyung Hee University, No. 1 Hoeki-Dong, Dongdaemoon-gu, Seoul 130-701, Republic of KoreaPM014 is a modified herbal formula based on Chung-Sang-Bo-Ha-Tang, which is a well-known prescription drug used for curing various inflammatory pulmonary diseases. We previously showed that PM014 attenuated lung inflammation in a murine model of chronic obstructive pulmonary disease (COPD). The objective of the present study was to evaluate the chronic oral toxicity of PM014 in rats. PM014 was administered to rats orally once daily at doses of 0, 750, 1500, and 3000 mg/kg/day for 13 weeks. The PM014 treatment did not result in any toxicologically significant changes between the control and treatment groups in body weight, clinical signs, food consumption, dermatological and serum biochemical parameters, organ weight ratio, or histopathology. We concluded that no PM014-related toxicity was detected even at the highest doses investigated in this repeated dose oral toxicity study. Based on our results, the no-observed-adverse-effect level (NOAEL) of PM014 was 3000 mg/kg/day in both genders. These results might provide supportive evidence of the safety of PM014 to develop a new drug.http://dx.doi.org/10.1155/2014/189673
collection DOAJ
language English
format Article
sources DOAJ
author Hwan-Suck Chung
Hyunil Lee
Hyunsu Bae
spellingShingle Hwan-Suck Chung
Hyunil Lee
Hyunsu Bae
Thirteen-Week Study of PM014 Subchronic Oral Toxicity in Rats
Evidence-Based Complementary and Alternative Medicine
author_facet Hwan-Suck Chung
Hyunil Lee
Hyunsu Bae
author_sort Hwan-Suck Chung
title Thirteen-Week Study of PM014 Subchronic Oral Toxicity in Rats
title_short Thirteen-Week Study of PM014 Subchronic Oral Toxicity in Rats
title_full Thirteen-Week Study of PM014 Subchronic Oral Toxicity in Rats
title_fullStr Thirteen-Week Study of PM014 Subchronic Oral Toxicity in Rats
title_full_unstemmed Thirteen-Week Study of PM014 Subchronic Oral Toxicity in Rats
title_sort thirteen-week study of pm014 subchronic oral toxicity in rats
publisher Hindawi Limited
series Evidence-Based Complementary and Alternative Medicine
issn 1741-427X
1741-4288
publishDate 2014-01-01
description PM014 is a modified herbal formula based on Chung-Sang-Bo-Ha-Tang, which is a well-known prescription drug used for curing various inflammatory pulmonary diseases. We previously showed that PM014 attenuated lung inflammation in a murine model of chronic obstructive pulmonary disease (COPD). The objective of the present study was to evaluate the chronic oral toxicity of PM014 in rats. PM014 was administered to rats orally once daily at doses of 0, 750, 1500, and 3000 mg/kg/day for 13 weeks. The PM014 treatment did not result in any toxicologically significant changes between the control and treatment groups in body weight, clinical signs, food consumption, dermatological and serum biochemical parameters, organ weight ratio, or histopathology. We concluded that no PM014-related toxicity was detected even at the highest doses investigated in this repeated dose oral toxicity study. Based on our results, the no-observed-adverse-effect level (NOAEL) of PM014 was 3000 mg/kg/day in both genders. These results might provide supportive evidence of the safety of PM014 to develop a new drug.
url http://dx.doi.org/10.1155/2014/189673
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