Fat reducing effects of Nelumbo nucifera leaf extract in overweight patients

2021 ◽  
pp. 1-6
Author(s):  
Luyi Ye ◽  
Xiaolin Wang ◽  
Tomonobu Konno ◽  
Xiangyu Gong ◽  
Hao Ding ◽  
...  
2015 ◽  
Vol 6 (3) ◽  
pp. 409-415 ◽  
Author(s):  
G. Premanand ◽  
N. Shanmugam ◽  
N. Kannadasan ◽  
K. Sathishkumar ◽  
G. Viruthagiri

Author(s):  
Enuo Liu ◽  
Hiroshi Tsuboi ◽  
Shuuji Ikegami ◽  
Tomonori Kamiyama ◽  
Yukio Asami ◽  
...  

Antioxidants ◽  
2019 ◽  
Vol 8 (9) ◽  
pp. 329 ◽  
Author(s):  
Mon-Yuan Yang ◽  
Tung-Wei Hung ◽  
Chau-Jong Wang ◽  
Tsui-Hwa Tseng

Leaf extract of Nelumbo nucifera (NLE) has been demonstrated to possess anti-atherosclerosis, improve alcohol-induced steatohepatitis, prevent high-fat diet-induced obesity, and inhibit the proliferation and metastasis of human breast cancer cells. This study determines the chemopreventive role of NLE against 2-acetylaminofluorene (AAF)-induced hepatocellular carcinoma (HCC) in rats. AAF was used to induce hepatocarcinogenesis in rats through genetic and nongenetic effects. After administration for 12 weeks, NLE (0.5–2%) supplementation orally inhibited AAF (0.03%)-induced hepatic fibrosis which appears during the development of premalignant lesions in rats. After the 6-month experiment, NLE supplementation resulted in decreasing AAF-induced serum parameters of hepatic injury, including the level of triglycerides, total cholesterol, alpha-fetoprotein (AFP), and inflammatory mediator interleukin (IL)-6 and tumor necrosis factor (TNF)-α as well as the activities of alanine aminotransferase (ALT), aspartate aminotransferase (AST), and gamma-glutamyl transferase (γGT). NLE supplementation also reduced AAF-induced lipid peroxidation and 8-hydroxy-2′-deoxyguanosine (8-OHdG) formation in the rat liver. Hepatic histopathological investigation revealed that NLE supplementation attenuated the AAF-induced HCC and glutathione S-transferase-Pi (GST-Pi) expression. Furthermore, NLE supplementation increased the expression of transcription factor, nuclear factor erythroid 2-related factor 2 (Nrf2) and its downstream targets, including catalase, glutathion peroxidase (GPx), and superoxide dismutase 1 (SOD-1) in the rat liver. Our findings indicate that NLE supplementation inhibited AAF-induced hepatocarcinogenesis by enhancing antioxidative potential and alleviating inflammation in rats.


2010 ◽  
Vol 108 (3) ◽  
pp. 693-702 ◽  
Author(s):  
Thirunavukkarasu Santhoshkumar ◽  
Abdul Abdul Rahuman ◽  
Govindasamy Rajakumar ◽  
Sampath Marimuthu ◽  
Asokan Bagavan ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (10) ◽  
pp. 3023
Author(s):  
Singeun Kim ◽  
Ki-Bae Hong ◽  
Kyungae Jo ◽  
Hyung Joo Suh

Current pharmacological treatments for insomnia carry several and long-term side effects. Therefore, natural products without side effects are warranted. In this study, the sleep-promoting activity of the lotus leaf (Nelumbo nucifera) extract was assessed using ICR mice and Sprague Dawley rats. A pentobarbital-induced sleep test and electroencephalogram analysis were conducted to measure sleep latency time, duration, and sleep architecture. The action mechanism of the extract was evaluated through ligand binding experiments. A high dose (300 mg/kg) of the ethanolic lotus leaf extract significantly increased sleep duration compared to the normal group (p < 0.01). Administration of low (150 mg/kg) and high doses (300 mg/kg) of the extract significantly increased sleep quality, especially the relative power of theta waves (p < 0.05), compared to the normal group. Furthermore, caffeine and lotus leaf extract administration significantly recovered caffeine-induced sleep disruption (p < 0.001), and the sleep quality was similar to that of the normal group. Additionally, ligand binding assay using [3H]-flumazenil revealed that quercetin-3-O-glucuronide contained in the lotus leaf extract (77.27 μg/mg of extract) enhanced sleep by binding to GABAA receptors. Collectively, these results indicated that the lotus leaf extract, particularly quercetin-3-O-glucuronide, exhibits sleep quantity- and quality-enhancing activity via the GABAergic pathway.


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