@article {2120, title = {The Effect of Syzygium Polyanthum (Wight) Walp. Extract on Glutathione, Tumour Necrosis Factor-Alpha, Spdl1, And Degraff Follicles Expression in PCOS Rat Models}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {791-800}, type = {Original Article}, chapter = {791}, abstract = {

Background: Polycystic ovary syndrome (PCOS) is an endocrine and reproductive disorder affecting 5\% to 13\% of women of reproductive age. Approximately 80\% of women with PCOS underwent infertility cases. Many studies have shown an association between PCOS and low-grade inflammation. Syzygium polyanthum (S. polyanthum) contains antioxidants and has antiinflammation activity. Objectives: This study aims to investigate the effectiveness of S. polyanthum leaf on glutathione, tumour necrosis factoralpha (TNF-α), sPDL1, and DeGraff follicle expression in PCOS rat models. Materials and Methods: The female Wistar rats were divided into five groups (n = 5), K0 (normal control), K1 (PCOS group), and three treatment groups which received three different doses of S. polyanthum extract. The treatment group consisted of PCOS rat models with S. polyanthum extract supplementation of 150 mg/KgBW (P1), 300 mg/KgBW (P2), and 450 mg/KgBW (P3). Results: S. polyanthum leaf extract significantly decreased TNF-α expression in the treatment group. The highest TNF-α, GSH, and sPDL1 concentration was found in the P3 group (3.83{\textpm}0.123, 273.12{\textpm}12.4 ng/ml, and 3.25 ng/ml, respectively). Moreover, the number of follicles was statistically significant in the P1, P2, and P3 groups (2.0, 3.0, and 3.50, respectively). The number of follicles in the P1, P2, and P3 groups was higher than in the positive control; however, it was lower in the negative control (K0) (p\<0.05). Conclusion: S. polyanthum extract was significantly effective in decreasing TNF-α expression, as well as a significant increase GSH, sPDL1 and DeGraff foliclle count in PCOS rat model.

}, keywords = {DeGraff follicle count, GSH, sPDL1, Syzygium polyanthum, TNF-.}, doi = {10.5530/pj.2023.15.154}, author = {Renny Aditya and Budi Santoso and Widjiati} } @article {1398, title = {Cardioprotective Role of Partharishtam on Isopreterenol Induced Myocardial Infarction in Animal Model}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {591-595}, type = {Research Article}, chapter = {591}, abstract = {

Myocardial infarction (MI) is one of the key causes of high death rate globally. We report the cardio protective effect of an Ayurvedic polyherbal formulation Partharishtam on isoproterenol induced myocardial infarction on albino rats. Administration of Isoproterenol to normal albino rat triggers MI evident from the significant changes in key biomolecules tested in blood serum and cardiac tissues. The cardio protective role of Partharishtam was compared with a standard medicine, Propranolol on some of the known identifying markers of MI such as, Troponin I and T, creatine phosphokinase serum (CPK-S), creatine phosphokinase myoglobulin isozyme fraction (CPK-MB) and oxidative enzymes like super oxide dismutase (SOD), reduced glutathione (GSH) and catalase. There was an appreciable decrease in the levels of Troponin 1 and T, CPK-S and CPK-MB after the treatment of Partharishtam on Isoproterenol induced MI rats. In vivo anti-oxidative enzyme studies also revealed the increase in the levels of SOD, GSH and catalase to near normalcy after the treatment of Partharishtam in MI rats, which is very much comparable to the commonly used drug Propranolol to treat MI patients. Histopathological analysis confirmed the cardio protective properties of Partharistham in rat model. We did not find any side effects or toxicity of Partharishtam when tested on the normal rats. Thus, polyherbal formulation Partharishtam could be considered as safe medicine for MI.

}, keywords = {Catalase, Creatine phosphokinase, GSH, Isoproterenol, Myocardial Infarction, Partharishtam, Polyherbal, Propranolol, SOD, Troponin I, Troponin T}, doi = {10.5530/pj.2021.13.74}, author = {G. Narayanan and K Prabhu and Anath Bandhu Chaudhury and Mudiganti Ram Krishna Rao and V S Kalai Selvi and N S Muthiah and Sruthi Dinakar} } @article {107, title = {Study of Protective Action of Spondias pinnata Bark extract on Rat Liver and Kidney against Etoposide Induced Chemical Stress}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {09/2015}, pages = {24-27}, type = {Original Article}, chapter = {24}, abstract = {

Introduction: System injury, manifested as metabolic dysfunction is a common side effect of chemotherapy. Chemical stress on hepatic and kidney cells can be evaluated by biochemical analysis, including serum aminotransferases, glutathione levels and extent of lipid peroxidation. Combined treatment of chemotherapy along with the natural products such as phytochemicals may be a newer approach to reduce the side effects and betterment of chemotherapy. Objective: The present study was conducted to assay kidney and liver associated parameters on animals exposed to etoposide, and the protective effect of different doses of Spondias pinnata bark extract on normal cells. In this study, total 24 male Wistar rats (either sex) aged between 60 to 90 days were considered. Each groups consisted of six rats. Levels of Alanine and Aspartate aminotransferases were estimated using semi-auto analyser and GSH, GST, TAO and LPx by spectrophotometry. Results and Conclusion: Data analyzed using Graph Pad 5.0. Variation in the analyzed parameters were found between control, chemotherapy and Spondias pinnata groups.\  Results of the study show that significant increase in TBARS levels indicative of etoposide induced oxidative stress could be prevented by the treatment with S. pinnata. GST levels also support the preventive action of S. pinnata against etoposide induced stress. However, TAO and transaminases remain unaltered in the study groups.

}, keywords = {Etoposide, GSH, GST, LPx, Spondias pinnata.}, doi = {10.5530/pj.2016.1.5}, author = {Beena Shetty and Gayathri Rao and Abhineetha and Niha Banu and Preethika and Sudarshan Reddy} }