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      Evaluation of Acute and Chronic Toxicities of the Water Extract from Ziziphus attopensis Pierre

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          Abstract

          We studied an acute and chronic oral toxicity of the extract from Ziziphus attopensis (ZA) in male and female SD rats according to the OECD guidelines. After a single oral administration of ZA 5 g/kg body weight, measurement of the body and organs, necropsy, and health monitoring were performed. The body and organ weights and behavior were not changed relative to the control rats indicating that ZA does not produce acute toxicity. The chronic toxicity was determined by oral feeding both male and female rats daily with ZA at the doses of 1, 2, 4, and 8 g/kg body weight for 180 days. Body weight changes, hematological and biochemical parameters, organ weights, gross finding, and histopathology examination were monitored during the experimental period. The results did not show any differences from the control groups. Analyses of these results with the information of signs, behavior, and health monitoring can lead to a conclusion that the long-term oral administration of ZA for 180 days does not cause chronic toxicity.

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          Is Open Access

          Effect of bee venom on some blood and biochemical parameters in formaldehyde induced arthritis male rats in comparison with prednisolone drug

          Background Bee venom(BV) has been used to treat and reduce chronic inflammatory diseases such as rheumatoid arthritis(RA), pain, skin diseases and to treat cancerous tumors. The aim of this study was to investigate the effects of bee venom on some blood and biochemical parameters in male albino rats with Arthritis and compare it with prednisolone drug. Materials & methods: (42) mature male albino rats (135-150) gm, divided into (7) groups, (6) male rats for each group. The experiment was continued for (14) days and included: the first group (negative control) was injected by (0.1ml/animal) from physiological normal saline (0.9% Nacl),the second group(Arthritis group) was injected by (0.1ml/animal) formaldehyde, the third group (normal group) was injected by bee venom(i.p) (1mg / kg of B.W), the fourth group (normal group) was treated orally with prednisolone (5mg / kg of B.W), the fifth group (Arthritis group) was injected by bee venom(i.p) (1mg / kg of B.W), the sixth group (Arthritis group) was treated orally by prednisolone (5 mg / kg of B.W) and seventh group (Arthritis group) was injected by bee venom (1 mg/ kg of B.W) and treated orally with prednisolone (5mg / kg of B.W). Results : Our results showed that 2 nd group (Arthritis) significantly increased (p≤ 0.05) in the number of WBCs and platelets compared with control group, while the 3 rd and 4 th groups showed a significant decrease in WBCs and PLT compared with 2 nd group. The 5 th , 6 th and 7 th groups showed a significant decrease (P≤0.05) in the number of WBCs and platelets compared with 2 nd group. On the other hand, the present study demonstrated a significant decrease (p≤ 0.05) in RBCs, hemoglobin (Hb) and hematocrit (HCT) in the 2 nd group (Arthritis group) compared with control group, while the 3 rd and 4 th groups showed a significant increase in RBCs, Hb and HCT compared with 2 nd group. The 5 th , 6 th and 7 th groups showed increase (p≤ 0.05) in RBCs, Hb and HCT compared with 2 nd group. The results showed also, a significant increase in levels of cholesterol, triglycerides, LDL and a significant decrease in HDL level in 2 nd group compared with control group, while 3 rd ,4 th , 5 th , 6 th and 7 th groups showed a significant decrease (P≤0.05) in cholesterol, triglycerides, LDL and a significant increase in HDL level compared with 2 nd group. Conclusion : We conclude from the present study that bee venom attenuates development of Arthritis by improving some Blood and Biochemical parameters.
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            Preliminary toxicity and phytochemical studies of the stem bark aqueous extract of Musanga cecropioides in rats.

            These studies were designed to determine the preliminary oral toxicity profile of the crude aqueous stem bark extract of Musanga cecropioides (MCW) in adult Sprague-Dawley rats and its active chemical constituents by way of phytochemistry. The acute oral toxicity study was conducted using limit dose test of Up and Down Procedure according to the OECD/OCDE Test Guidelines on Acute Oral Toxicity (AOT425statPgm, version: 1.0) at a limit dose of 3,000 mg/kg body weight/oral route. Repeat dose oral toxicity studies were conducted by daily oral dosing of 750 mg/kg body weight of MCW dissolved in 1 ml of 0.9% saline and 1 ml of 0.9% saline to rats in the test and control groups, respectively, for 28 days. On day 29, blood samples for bioassays were collected by cardiac puncture under diethyl ether anesthesia. The phytochemical analysis was conducted using standard procedures. The LD(50) estimate of the extract was calculated to be greater than 3,000 mg/kg body weight/oral route. The extract caused a significant (P<0.05) decrease in weight gain, differential eosinophil count and increase in serum creatinine but did not affect the organ weights, other serum electrolytes (Na(+), K(+), HCO(3)(-)), liver enzymes and other hematological indices in test rats. Its phytochemical analysis showed it contains saponins, flavonoids, alkaloids, tannins, phlobatannins, glycosides, reducing sugars and anthraquinones. These results show that the aqueous extract of Musanga cecropioides is relatively safe toxicologically when administered orally. Thus, its use in folkloric medicine as an oral antihypertensive is relatively safe when used over the tested period.
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              Estimation of acute oral toxicity in rats by determination of the approximate lethal dose rather than the LD50.

              The approximate lethal dose (ALD) to rats following oral administration of nine chemicals was determined. The ALD (lowest dose at which death was produced) for each chemical was used to define the general order of toxicity as being either extremely, highly, moderately, slightly, or practically non-toxic. For each of the nine chemicals tested, the category indicated by the ALD was identical with the category determined in the more extensive LD50 studies. In this study, an average of 6.8 rats was needed to determine the ALD while an average of 56.3 rats was needed to determine the LD50.
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                Author and article information

                Journal
                ISRN Pharmacol
                ISRN Pharmacol
                ISRN.PHARMACOLOGY
                ISRN Pharmacology
                International Scholarly Research Network
                2090-5165
                2090-5173
                2012
                20 March 2012
                : 2012
                : 789651
                Affiliations
                1Division of Pharmacology, Department of Preclinical Science, Faculty of Medicine, Thammasat University, Pathumthani 12120, Thailand
                2Division of Physiology, Department of Preclinical Science, Faculty of Medicine, Thammasat University, Pathumthani 12120, Thailand
                3Department of Animal Science, Faculty of Agricultural Technology, Chiang Mai Rajabhat University, Chiang Mai 50300, Thailand
                4Department of Pharmacology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand
                Author notes
                *Seewaboon Sireeratawong: seewaboon@ 123456gmail.com

                Academic Editors: H. Cerecetto and A. Pittaluga

                Article
                10.5402/2012/789651
                3317065
                22474597
                e97a34a4-49de-4d7b-88c3-992b4145c325
                Copyright © 2012 Seewaboon Sireeratawong et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 November 2011
                : 19 December 2011
                Categories
                Research Article

                Pharmacology & Pharmaceutical medicine
                Pharmacology & Pharmaceutical medicine

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