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      Acute, chronic, and genotoxic studies on the protopine total alkaloids of the Macleaya cordata (willd.) R. Br. in rodents

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          Abstract

          The protopine alkaloids are widely distributed within the opium poppy family and have a wide range of pharmacological effects. MPTA is a product of the protopine total alkaloids extracted from the Macleaya cordata (Willd.) R. Br. Previously, we reported good anti-inflammatory activity of MPTA as well as oral acute and sub-chronic toxicity studies in rats. In order to perform a systematic toxicological safety assessment of MPTA, oral acute toxicity, genotoxicity (bone marrow cell chromosome aberration test, sperm abnormality test, bone marrow cell micronucleus test, and rat teratogenicity test), and chronic toxicity in mice were performed in this study. In the oral acute toxicity test, the LD 50 in ICR mice was 481.99 mg/kg, with 95% confidence limits ranging from 404.27 to 574.70 mg/kg. All three mutagenicity tests tested negative in the range of 60.25–241.00 mg/kg. The results of the teratogenicity test in rats showed no reproductive or embryonic developmental toxicity at only 7.53 mg/kg, which can be considered as a no observed effect level (NOEL) for the teratogenicity test. Therefore, MPTA is safe for use at the doses tested, but attention should be paid to the potential risk to pregnant animals and the safety evaluation and toxicity mechanisms in target animals should be further investigated.

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          Most cited references45

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          Pathophysiological aspects of nephropathy caused by non-steroidal anti-inflammatory drugs

          Abstract Non-steroidal anti-inflammatory drugs (NSAIDs) are commonly used medications associated with nephrotoxicity, especially when used chronically. Factors such as advanced age and comorbidities, which in themselves already lead to a decrease in glomerular filtration rate, increase the risk of NSAID-related nephrotoxicity. The main mechanism of NSAID action is cyclooxygenase (COX) enzyme inhibition, interfering on arachidonic acid conversion into E2 prostaglandins E2, prostacyclins and thromboxanes. Within the kidneys, prostaglandins act as vasodilators, increasing renal perfusion. This vasodilatation is a counter regulation of mechanisms, such as the renin-angiotensin-aldosterone system works and that of the sympathetic nervous system, culminating with compensation to ensure adequate flow to the organ. NSAIDs inhibit this mechanism and can lead to acute kidney injury (AKI). High doses of NSAIDs have been implicated as causes of AKI, especially in the elderly. The main form of AKI by NSAIDs is hemodynamically mediated. The second form of NSAID-induced AKI is acute interstitial nephritis, which may manifest as nephrotic proteinuria. Long-term NSAID use can lead to chronic kidney disease (CKD). In patients without renal diseases, young and without comorbidities, NSAIDs are not greatly harmful. However, because of its dose-dependent effect, caution should be exercised in chronic use, since it increases the risk of developing nephrotoxicity.
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            Aspirin use during pregnancy and the risk of bleeding complications: A Swedish population-based cohort study.

            Aspirin is offered to pregnant women to prevent preeclampsia, a severe obstetrical complication. Large studies of nonpregnant populations have consistently shown that aspirin prophylaxis increases the risk of hemorrhagic complications. However, there have not been any population-based studies investigating this in a pregnant population.
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              Protopine reduces the inflammatory activity of lipopolysaccharide-stimulated murine macrophages.

              Protopine is an isoquinoline alkaloid contained in plants in northeast Asia. In this study, we investigated whether protopine derived from Hypecoum erectum L could suppress lipopolysaccharide (LPS)-induced inflammatory responses in murine macrophages (Raw 264.7 cells). Protopine was found to reduce nitric oxide (NO), cyclooxygenase-2 (COX-2), and prostaglandin E(2) (PGE(2)) production by LPS-stimulated Raw 264.7 cells, without a cytotoxic effect. Pre-treatment of Raw 264.7 cells with protopine reduced the production of pro-inflammatory cytokines. These inhibitory effects were caused by blocking phosphorylation of mitogen-activated protein kinases (MAP kinases) and also blocking activation of a nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB).
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                Author and article information

                Contributors
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                28 September 2022
                2022
                : 13
                : 987800
                Affiliations
                [1] 1 College of Veterinary Medicine , Hunan Agricultural University , Changsha, China
                [2] 2 Key Laboratory of Chinese Veterinary Medicine in Hunan Province , Hunan Agricultural University , Changsha, China
                [3] 3 College of Veterinary Medicine , China Agricultural University , Beijing, China
                [4] 4 College of Veterinary Medicine , Shanxi Agricultural University , Jinzhong, China
                [5] 5 Hunan MICOLTA Biological Resources Co.,Ltd , Changsha, China
                Author notes

                Edited by: Fareeha Anwar, Riphah International University (Lahore), Pakistan

                Reviewed by: Qurat Ul Ain, Riphah International University (Lahore), Pakistan

                Uzma Saleem, Government College University, Pakistan

                *Correspondence: Zi-hui Yang, yangzihui_2021@ 123456hunau.edu.cn ; Jian-guo Zeng, zengjianguo@ 123456hunau.edu.cn

                This article was submitted to Predictive Toxicology, a section of the journal Frontiers in Pharmacology

                Article
                987800
                10.3389/fphar.2022.987800
                9554591
                36249819
                0f4d8f82-c271-426f-96d0-f8e6a85a162d
                Copyright © 2022 Dong, Tang, Ma, Tan, Tang, Li, Yang and Zeng.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 06 July 2022
                : 06 September 2022
                Categories
                Pharmacology
                Original Research

                Pharmacology & Pharmaceutical medicine
                macleaya cordata (willd.) r. br.,protopine alkaloids,acute toxicity,chronic toxicity,mutagenicity,teratogenicity,reproductive toxicity,embryonic developmental toxicity

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