Toxicological safety evaluation of Qin-Zhi-Zhu-Dan formula in rats during the treatment and recovery periods
Background: Qinzhi Zhudan Formula (QZZD), optimized from Angong Niuhuang Wan, consists of Radix Scutellariae, Fructus Gardeniae and Pulvis Fellis Suis. We had investigated the neuroprotective effects of QZZD and its active components, and demonstrated that it could treat cerebral ischemia and dement...
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Frontiers Media S.A.
2022-08-01
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| Series: | Frontiers in Pharmacology |
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| Online Access: | https://www.frontiersin.org/articles/10.3389/fphar.2022.987997/full |
| _version_ | 1798036675948969984 |
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| author | Wenxiu Xu Dan Chen Zehan Zhang Shuling Liu Congai Chen Chunyan Sun Wenchao Ni Xiangdong Kang Guojiao Shang Xueqian Wang Fafeng Cheng Qingguo Wang |
| author_facet | Wenxiu Xu Dan Chen Zehan Zhang Shuling Liu Congai Chen Chunyan Sun Wenchao Ni Xiangdong Kang Guojiao Shang Xueqian Wang Fafeng Cheng Qingguo Wang |
| author_sort | Wenxiu Xu |
| collection | DOAJ |
| description | Background: Qinzhi Zhudan Formula (QZZD), optimized from Angong Niuhuang Wan, consists of Radix Scutellariae, Fructus Gardeniae and Pulvis Fellis Suis. We had investigated the neuroprotective effects of QZZD and its active components, and demonstrated that it could treat cerebral ischemia and dementia through multiple pathways and mechanisms. Nevertheless, toxicological data on this formula still remains limited. In the study, we sought to examine the toxicological effects of QZZD during the treatment and recovery periods.Methods: We investigated potential toxicities of QZZD in Sprague-Dawley (SD) rats via 28-day gavage administration. SD rats were randomly divided into control group and treatment groups of A (0.5 g/kg/d QZZD), B (1.5 g/kg/d QZZD), and C (5.0 g/kg/d QZZD). The 56-day course includes treatment period (administration with water or QZZD once a day for 28 consecutive days) and recovery period (28 days). The rats received daily monitoring of general signs of toxicity and mortality, as well as weekly determination of body weight and food consumption. Moreover, the complete blood cell count, biochemistry, coagulation, and urine indicators, organ weights, and histopathological report were analyzed respectively at the end of the treatment and recovery periods.Results: There was no death related to the active pharmaceutical ingredients of QZZD during the treatment period. The maximum no observed adverse effect level (NOAEL) was 0.5 g/kg/d, which is approximately 16.7 times of the equivalent dose of clinical dose in rats. In group TB (1.5 g/kg/d QZZD) and TC (5.0 g/kg/d QZZD), there were adverse effects of blue coloring of tail skin, weight loss, a significant increase of total bilirubin (TBIL), blackening of liver and kidney in gross examination, hyperplasia of bile duct and karyomegaly of hepatocytes in histopathological examination. Besides, in females rats, the food consumption was reduced, while in male rats, there was decrease in triglycerides (TG) and slight increase in white blood cell (WBC) count and neutrophils. In group TC (5.0 g/kg/d QZZD), the indicators of red blood cell (RBC) count, hemoglobin (HGB) and hematocrit (HCT) were decreased slightly, while the platelet count (PLT) was increased. However, these changes were not considered to be toxicologically significant because they resolved during the recovery period.Conclusion: Overall, QZZD exhibited a good safety profile. The maximum no observed adverse effect level was 0.5 g/kg/d, and no target organs toxicity were identified. The present findings might confirm the safety of QZZD in clinical practices. |
| first_indexed | 2024-04-11T21:16:12Z |
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| language | English |
| last_indexed | 2024-04-11T21:16:12Z |
| publishDate | 2022-08-01 |
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| spelling | doaj.art-e2ab45ca30ca4f368fbbde193792ec8d2022-12-22T04:02:49ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122022-08-011310.3389/fphar.2022.987997987997Toxicological safety evaluation of Qin-Zhi-Zhu-Dan formula in rats during the treatment and recovery periodsWenxiu Xu0Dan Chen1Zehan Zhang2Shuling Liu3Congai Chen4Chunyan Sun5Wenchao Ni6Xiangdong Kang7Guojiao Shang8Xueqian Wang9Fafeng Cheng10Qingguo Wang11School of Traditional Chinese Medicine Department, Beijing University of Chinese Medicine, Beijing, ChinaSchool of Traditional Chinese Medicine Department, Beijing University of Chinese Medicine, Beijing, ChinaSchool of Traditional Chinese Medicine Department, Beijing University of Chinese Medicine, Beijing, ChinaSchool of Traditional Chinese Medicine Department, Beijing University of Chinese Medicine, Beijing, ChinaDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, ChinaDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, ChinaDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, ChinaSchool of Traditional Chinese Medicine Department, Beijing University of Chinese Medicine, Beijing, ChinaSchool of Traditional Chinese Medicine Department, Beijing University of Chinese Medicine, Beijing, ChinaSchool of Traditional Chinese Medicine Department, Beijing University of Chinese Medicine, Beijing, ChinaSchool of Traditional Chinese Medicine Department, Beijing University of Chinese Medicine, Beijing, ChinaSchool of Traditional Chinese Medicine Department, Beijing University of Chinese Medicine, Beijing, ChinaBackground: Qinzhi Zhudan Formula (QZZD), optimized from Angong Niuhuang Wan, consists of Radix Scutellariae, Fructus Gardeniae and Pulvis Fellis Suis. We had investigated the neuroprotective effects of QZZD and its active components, and demonstrated that it could treat cerebral ischemia and dementia through multiple pathways and mechanisms. Nevertheless, toxicological data on this formula still remains limited. In the study, we sought to examine the toxicological effects of QZZD during the treatment and recovery periods.Methods: We investigated potential toxicities of QZZD in Sprague-Dawley (SD) rats via 28-day gavage administration. SD rats were randomly divided into control group and treatment groups of A (0.5 g/kg/d QZZD), B (1.5 g/kg/d QZZD), and C (5.0 g/kg/d QZZD). The 56-day course includes treatment period (administration with water or QZZD once a day for 28 consecutive days) and recovery period (28 days). The rats received daily monitoring of general signs of toxicity and mortality, as well as weekly determination of body weight and food consumption. Moreover, the complete blood cell count, biochemistry, coagulation, and urine indicators, organ weights, and histopathological report were analyzed respectively at the end of the treatment and recovery periods.Results: There was no death related to the active pharmaceutical ingredients of QZZD during the treatment period. The maximum no observed adverse effect level (NOAEL) was 0.5 g/kg/d, which is approximately 16.7 times of the equivalent dose of clinical dose in rats. In group TB (1.5 g/kg/d QZZD) and TC (5.0 g/kg/d QZZD), there were adverse effects of blue coloring of tail skin, weight loss, a significant increase of total bilirubin (TBIL), blackening of liver and kidney in gross examination, hyperplasia of bile duct and karyomegaly of hepatocytes in histopathological examination. Besides, in females rats, the food consumption was reduced, while in male rats, there was decrease in triglycerides (TG) and slight increase in white blood cell (WBC) count and neutrophils. In group TC (5.0 g/kg/d QZZD), the indicators of red blood cell (RBC) count, hemoglobin (HGB) and hematocrit (HCT) were decreased slightly, while the platelet count (PLT) was increased. However, these changes were not considered to be toxicologically significant because they resolved during the recovery period.Conclusion: Overall, QZZD exhibited a good safety profile. The maximum no observed adverse effect level was 0.5 g/kg/d, and no target organs toxicity were identified. The present findings might confirm the safety of QZZD in clinical practices.https://www.frontiersin.org/articles/10.3389/fphar.2022.987997/fullsub-chronic toxicityscutellaria baicalensis extractgardenia extractpulvis fellis suisreversibility studyorgan coefficient |
| spellingShingle | Wenxiu Xu Dan Chen Zehan Zhang Shuling Liu Congai Chen Chunyan Sun Wenchao Ni Xiangdong Kang Guojiao Shang Xueqian Wang Fafeng Cheng Qingguo Wang Toxicological safety evaluation of Qin-Zhi-Zhu-Dan formula in rats during the treatment and recovery periods Frontiers in Pharmacology sub-chronic toxicity scutellaria baicalensis extract gardenia extract pulvis fellis suis reversibility study organ coefficient |
| title | Toxicological safety evaluation of Qin-Zhi-Zhu-Dan formula in rats during the treatment and recovery periods |
| title_full | Toxicological safety evaluation of Qin-Zhi-Zhu-Dan formula in rats during the treatment and recovery periods |
| title_fullStr | Toxicological safety evaluation of Qin-Zhi-Zhu-Dan formula in rats during the treatment and recovery periods |
| title_full_unstemmed | Toxicological safety evaluation of Qin-Zhi-Zhu-Dan formula in rats during the treatment and recovery periods |
| title_short | Toxicological safety evaluation of Qin-Zhi-Zhu-Dan formula in rats during the treatment and recovery periods |
| title_sort | toxicological safety evaluation of qin zhi zhu dan formula in rats during the treatment and recovery periods |
| topic | sub-chronic toxicity scutellaria baicalensis extract gardenia extract pulvis fellis suis reversibility study organ coefficient |
| url | https://www.frontiersin.org/articles/10.3389/fphar.2022.987997/full |
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