Effect of isoproterenol and thyroxine in herbal drug used as cardiac hypertrophy

Q4 Medicine
Arjesh Raj, S. Tyagi, R. Kumar, A. Dubey, Anurag C Hourasia
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引用次数: 21

Abstract

The impact of A. calamus extract and C. Pereira extract on heart hypertrophy caused by isoproterenol. A. calamus extract & C. Pereira extract on heart hypertrophy by thyroxine. MATERIAL AND METHOD a. Animal House Pharmacy School (Wistar rats), measuring 180-250 grammes, BIT Meerut (UP). One week before the research began, they were kept separately in polypropylene cages in a quarantine room. b. C. Pareira and A. calamus rhizomes from the School of Pharmacy at the Medicinal Garden, BIT, Merrut, UP, India. METHODS  Influence of C. Pareria Extract on Isoproterenol- induced cardiac hypertrophy in rats.  Influence of A. Calamus Extract on Isoproterenol- induced cardiac hypertrophy in rats. Influence of C. Pareria Extract on Thyroxine- induced cardiac hypertrophy in rats  Influence of A Calamus Extract on Thyroxine- induced cardiac hypertrophy in rats. RESULTS In comparison with control and C. Pareira and A. Calamus as well as amlodipine treated groups in the ISO treatment community, no major alteration was identified in the MAP. There was no MAP change in T4 compared with controls and groups C. pareira and amlodipine treated with T4. Significantly increased T4 (P < O.O1) HR administration against power.No significant change in HR was detected in C. Pareira and A. calamus. CONCULSION Cissampelos pareira and Acorn calamus effect in cardiac hypertrophy induced by isoproterenol Isoproterenol chronic administration (5 mg/lcg/day, 30 days), cardiac hypertrophy, cardiac weight ratio, angiotensin II, tumour factor necrosis, calcineurin, oxide/reactive nitrients, NaV K'^-ATPase, antioxidant and NaVK'^-ATPase, active component antioxidants Both of these changes in the therapy of Cissampelos pareira (100 and 200 mg/kg/day, 30 days) and Acorus calamus (100 and 200 mg/kg/day, 30 days) were substantially enhanced. Effect of thyroxin-induced cardiac hypertrophy on Cissampelos pareira and Acorus calamus The continuous thyroxine (0.1 mg/kg/day, for 30 days) was characterised by hypertropy of the heart and heart and body weight ratios, Angiotensin II, tumour necrosis factor, calcineurine, nitric oxide and thyrobarbituric acid, and a substantial decrease. Hypertrophy of the heart Cissampelos pareira (100 and 200 mg/kg/day) and Acorus calamus (100 and 200 mG/kg/day) have been decreased to almost normal in the next 30 days.
异丙肾上腺素和甲状腺素在中药治疗心肌肥厚中的作用
菖蒲提取物和菖蒲提取物对异丙肾上腺素所致心脏肥厚的影响。菖蒲提取物和佩雷拉提取物对甲状腺素致心脏肥厚的影响。a.动物之家药学院(Wistar大鼠),量180-250克,BIT Meerut (UP)。在研究开始前一周,他们被分别关在隔离室的聚丙烯笼子里。b. C. Pareira和A.菖蒲根状茎,产自印度北方邦梅鲁特BIT药用花园药学院。方法:枳实提取物对异丙肾上腺素所致大鼠心肌肥厚的影响。菖蒲提取物对异丙肾上腺素诱导大鼠心肌肥厚的影响。枳实提取物对甲状腺素致大鼠心肌肥厚的影响——菖蒲提取物对甲状腺素致大鼠心肌肥厚的影响。结果与对照组、异源性肾上腺素治疗组、异源性肾上腺素治疗组和氨氯地平治疗组相比,MAP未见明显变化。与对照组、帕雷拉组和氨氯地平组相比,T4 MAP无变化。HR给药对功率的影响显著增加T4 (P < 0.01)。赤芍和菖蒲的HR未见明显变化。结论异丙肾上腺素慢性给药(5 mg/lcg/d, 30 d)、心脏肥厚、心脏重量比、血管紧张素II、肿瘤因子坏死、钙调磷酸酶、氧化物/活性营养素、NaVK′^- atp酶、抗氧化剂和NaVK′^- atp酶、活性成分抗氧化剂均在异丙肾上腺素治疗(100和200 mg/kg/d)时发生变化。菖蒲(100和200 mg/kg/天,30天)显著提高。持续使用甲状腺素(0.1 mg/kg/d,连用30天),表现为心脏肥大,心重比、血管紧张素II、肿瘤坏死因子、钙调碱、一氧化氮、甲状巴比妥酸均显著降低。在接下来的30天内,山菖蒲(100和200 mg/kg/天)和菖蒲(100和200 mg/kg/天)的心脏肥厚已降至几乎正常。
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来源期刊
Journal of Cardiovascular Disease Research
Journal of Cardiovascular Disease Research Medicine-Cardiology and Cardiovascular Medicine
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