1.Clinical experience of high-flow nasal cannula oxygen therapy in severe COVID-19 patients.
Guojun HE ; Yijiao HAN ; Qiang FANG ; Jianying ZHOU ; Jifang SHEN ; Tong LI ; Qibin PU ; Aijun CHEN ; Zhiyang QI ; Lijun SUN ; Hongliu CAI
Journal of Zhejiang University. Medical sciences 2020;49(2):232-239
		                        		
		                        			
		                        			Acute respiratory failure due to acute hypoxemia is the major manifestation in severe coronavirus disease 2019 (COVID-19). Rational and effective respiratory support is crucial in the management of COVID-19 patients. High-flow nasal cannula (HFNC) has been utilized widely due to its superiority over other non-invasive respiratory support techniques. To avoid HFNC failure and intubation delay, the key issues are proper patients, timely application and improving compliance. It should be noted that elder patients are vulnerable for failed HFNC. We applied HFNC for oxygen therapy in severe and critical ill COVID-19 patients and summarized the following experiences. Firstly, to select the proper size of nasal catheter, to locate it at suitable place, and to confirm the nose and the upper respiratory airway unobstructed. Secondly, an initial ow of 60 L/min and 37℃ should be given immediately for patients with obvious respiratory distress or weak cough ability; otherwise, low-level support should be given first and the level gradually increased. Thirdly, to avoid hypoxia or hypoxemia, the treatment goal of HFNC should be maintained the oxygen saturation (SpO) above 95% for patients without chronic pulmonary disease. Finally, patients should wear a surgical mask during HFNC treatment to reduce the risk of virus transmission through droplets or aerosols.
		                        		
		                        		
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Betacoronavirus
		                        			;
		                        		
		                        			isolation & purification
		                        			;
		                        		
		                        			Cannula
		                        			;
		                        		
		                        			Coronavirus Infections
		                        			;
		                        		
		                        			therapy
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Oxygen
		                        			;
		                        		
		                        			administration & dosage
		                        			;
		                        		
		                        			Pandemics
		                        			;
		                        		
		                        			Pneumonia, Viral
		                        			;
		                        		
		                        			therapy
		                        			
		                        		
		                        	
2.Clinical experience of high-flow nasal cannula oxygen therapy in severe corona virus disease 2019 (COVID-19) patients.
Guojun HE ; Yijiao HAN ; Qiang FANG ; Jianying ZHOU ; Jifang SHEN ; Tong LI ; Qibin PU ; Aijun CHEN ; Zhiyang QI ; Lijun SUN ; Hongliu CAI
Journal of Zhejiang University. Medical sciences 2020;49(1):232-239
		                        		
		                        			
		                        			Acute respiratory failure due to acute hypoxemia is the major manifestation in severe coronavirus disease 2019 (COVID-19) induced by severe acute respiratory syndrome coronavirus 2 infection. Rational and effective respiratory support is crucial in the management of COVID-19 patients. High-flow nasal cannula (HFNC) has been utilized widely due to its superiority over other non-invasive respiratory support techniques. To avoid HFNC failure and intubation delay, the key issues are proper patients, timely application and improving compliance. It should be noted that elder patients are vulnerable for failed HFNC. We applied HFNC for oxygen therapy in severe and critical COVID-19 patients and summarized the following experiences. Firstly, to select the proper size of nasal catheter, to locate it at suitable place, and to confirm the nose and the upper respiratory airway unobstructed. Secondly, an initial flow of 60 L/min and 37℃ should be given immediately for patients with obvious respiratory distress or weak cough ability; otherwise, low-level support should be given first and the level gradually increased. Thirdly, to avoid hypoxia or hypoxemia, the treatment goal of HFNC should be maintained the oxygen saturation (SpO) above 95% for patients without chronic pulmonary disease. Finally, patients should wear a surgical mask during HFNC treatment to reduce the risk of virus transmission through droplets or aerosols.
		                        		
		                        		
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Betacoronavirus
		                        			;
		                        		
		                        			Cannula
		                        			;
		                        		
		                        			Coronavirus Infections
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			therapy
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Hypoxia
		                        			;
		                        		
		                        			etiology
		                        			;
		                        		
		                        			prevention & control
		                        			;
		                        		
		                        			therapy
		                        			;
		                        		
		                        			Masks
		                        			;
		                        		
		                        			Oxygen
		                        			;
		                        		
		                        			administration & dosage
		                        			;
		                        		
		                        			Oxygen Inhalation Therapy
		                        			;
		                        		
		                        			instrumentation
		                        			;
		                        		
		                        			standards
		                        			;
		                        		
		                        			Pandemics
		                        			;
		                        		
		                        			Pneumonia, Viral
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			therapy
		                        			
		                        		
		                        	
3.Inhibition of chemotherapy-related breast tumor EMT by application of redox-sensitive siRNA delivery system CSO-ss-SA/siRNA along with doxorubicin treatment.
Xuan LIU ; Xue-Qing ZHOU ; Xu-Wei SHANG ; Li WANG ; Yi LI ; Hong YUAN ; Fu-Qiang HU
Journal of Zhejiang University. Science. B 2020;21(3):218-233
		                        		
		                        			
		                        			Metastasis is one of the main reasons causing death in cancer patients. It was reported that chemotherapy might induce metastasis. In order to uncover the mechanism of chemotherapy-induced metastasis and find solutions to inhibit treatment-induced metastasis, the relationship between epithelial-mesenchymal transition (EMT) and doxorubicin (DOX) treatment was investigated and a redox-sensitive small interfering RNA (siRNA) delivery system was designed. DOX-related reactive oxygen species (ROS) were found to be responsible for the invasiveness of tumor cells in vitro, causing enhanced EMT and cytoskeleton reconstruction regulated by Ras-related C3 botulinum toxin substrate 1 (RAC1). In order to decrease RAC1, a redox-sensitive glycolipid drug delivery system (chitosan-ss-stearylamine conjugate (CSO-ss-SA)) was designed to carry siRNA, forming a gene delivery system (CSO-ss-SA/siRNA) downregulating RAC1. CSO-ss-SA/siRNA exhibited an enhanced redox sensitivity compared to nonresponsive complexes in 10 mmol/L glutathione (GSH) and showed a significant safety. CSO-ss-SA/siRNA could effectively transmit siRNA into tumor cells, reducing the expression of RAC1 protein by 38.2% and decreasing the number of tumor-induced invasion cells by 42.5%. When combined with DOX, CSO-ss-SA/siRNA remarkably inhibited the chemotherapy-induced EMT in vivo and enhanced therapeutic efficiency. The present study indicates that RAC1 protein is a key regulator of chemotherapy-induced EMT and CSO-ss-SA/siRNA silencing RAC1 could efficiently decrease the tumor metastasis risk after chemotherapy.
		                        		
		                        		
		                        		
		                        			Amines/chemistry*
		                        			;
		                        		
		                        			Antineoplastic Agents/adverse effects*
		                        			;
		                        		
		                        			Breast Neoplasms/pathology*
		                        			;
		                        		
		                        			Chitosan/chemistry*
		                        			;
		                        		
		                        			Doxorubicin/adverse effects*
		                        			;
		                        		
		                        			Drug Delivery Systems
		                        			;
		                        		
		                        			Epithelial-Mesenchymal Transition/drug effects*
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			MCF-7 Cells
		                        			;
		                        		
		                        			Neoplasm Metastasis/prevention & control*
		                        			;
		                        		
		                        			Oxidation-Reduction
		                        			;
		                        		
		                        			RNA, Small Interfering/administration & dosage*
		                        			;
		                        		
		                        			Reactive Oxygen Species/metabolism*
		                        			;
		                        		
		                        			rac1 GTP-Binding Protein/physiology*
		                        			
		                        		
		                        	
4.Chronic Intracerebroventricular Infusion of Metformin Inhibits Salt-Sensitive Hypertension via Attenuation of Oxidative Stress and Neurohormonal Excitation in Rat Paraventricular Nucleus.
Xiao-Jing YU ; Ya-Nan ZHAO ; Yi-Kang HOU ; Hong-Bao LI ; Wen-Jie XIA ; Hong-Li GAO ; Kai-Li LIU ; Qing SU ; Hui-Yu YANG ; Bin LIANG ; Wen-Sheng CHEN ; Wei CUI ; Ying LI ; Guo-Qing ZHU ; Zhi-Ming YANG ; Yu-Ming KANG
Neuroscience Bulletin 2019;35(1):57-66
		                        		
		                        			
		                        			Metformin (MET), an antidiabetic agent, also has antioxidative effects in metabolic-related hypertension. This study was designed to determine whether MET has anti-hypertensive effects in salt-sensitive hypertensive rats by inhibiting oxidative stress in the hypothalamic paraventricular nucleus (PVN). Salt-sensitive rats received a high-salt (HS) diet to induce hypertension, or a normal-salt (NS) diet as control. At the same time, they received intracerebroventricular (ICV) infusion of MET or vehicle for 6 weeks. We found that HS rats had higher oxidative stress levels and mean arterial pressure (MAP) than NS rats. ICV infusion of MET attenuated MAP and reduced plasma norepinephrine levels in HS rats. It also decreased reactive oxygen species and the expression of subunits of NAD(P)H oxidase, improved the superoxide dismutase activity, reduced components of the renin-angiotensin system, and altered neurotransmitters in the PVN. Our findings suggest that central MET administration lowers MAP in salt-sensitive hypertension via attenuating oxidative stress, inhibiting the renin-angiotensin system, and restoring the balance between excitatory and inhibitory neurotransmitters in the PVN.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Antioxidants
		                        			;
		                        		
		                        			therapeutic use
		                        			;
		                        		
		                        			Arterial Pressure
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			Hypertension
		                        			;
		                        		
		                        			chemically induced
		                        			;
		                        		
		                        			drug therapy
		                        			;
		                        		
		                        			Infusions, Intraventricular
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Metformin
		                        			;
		                        		
		                        			administration & dosage
		                        			;
		                        		
		                        			pharmacology
		                        			;
		                        		
		                        			Neurotransmitter Agents
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Oxidative Stress
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			Paraventricular Hypothalamic Nucleus
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			Rats
		                        			;
		                        		
		                        			Reactive Oxygen Species
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Sodium Chloride, Dietary
		                        			;
		                        		
		                        			pharmacology
		                        			
		                        		
		                        	
5.Effects of ZJ0273 on barley and growth recovery of herbicide-stressed seedlings through application of branched-chain amino acids.
Ling XU ; Jian-Yao SHOU ; Rafaqat Ali GILL ; Xiang GUO ; Ullah NAJEEB ; Wei-Jun ZHOU
Journal of Zhejiang University. Science. B 2019;20(1):71-83
		                        		
		                        			
		                        			In this study, we evaluated the effect of the herbicide propyl 4-(2-(4,6-dimethoxypyrimidin-2-yloxy)benzylamino) benzoate (ZJ0273) on barley growth and explored the potential to trigger growth recovery through the application of branched-chain amino acids (BCAAs). Barley plants were foliar-sprayed with various concentrations of ZJ0273 (100, 500, or 1000 mg/L) at the four-leaf stage. Increasing either the herbicide concentration or measurement time after herbicide treatment significantly impaired plant morphological parameters such as plant height and biomass, and affected physiological indexes, i.e. maximal photochemical efficiency (Fv/Fm), quantum yield of photosystem II (ФPSII), net photosynthetic rate (Pn), and chlorophyll meter value (soil and plant analyzer development (SPAD)). Cellular injury of herbicide-treated plants was also evidenced by increased levels of reactive oxygen species (ROS) and antioxidative enzyme activity. Elevated levels of herbicide significantly reduced the activity of acetolactate synthase (ALS)-a key enzyme in the biosynthesis of BCAAs. In a separate experiment, growth recovery in herbicide-stressed barley plants was studied using various concentrations of BCAAs (10, 50, 100, and 200 mg/L). Increasing BCAA concentration in growth media significantly increased the biomass of herbicide-stressed barley seedlings, but had no significant effect on non-stressed plants. Further, BCAAs (100 mg/L) significantly down-regulated ROS and consequently antioxidant enzyme levels in herbicide-stressed plants. Our results showed that exogenous application of BCAAs could reverse the inhibitory effects of ZJ0273 by restoring protein biosynthesis in barley seedlings.
		                        		
		                        		
		                        		
		                        			Amino Acids, Branched-Chain/administration & dosage*
		                        			;
		                        		
		                        			Antioxidants/metabolism*
		                        			;
		                        		
		                        			Benzoates/pharmacology*
		                        			;
		                        		
		                        			Biomass
		                        			;
		                        		
		                        			Chlorophyll/metabolism*
		                        			;
		                        		
		                        			Herbicides/pharmacology*
		                        			;
		                        		
		                        			Hordeum/metabolism*
		                        			;
		                        		
		                        			Photosynthesis/drug effects*
		                        			;
		                        		
		                        			Plant Leaves/metabolism*
		                        			;
		                        		
		                        			Reactive Oxygen Species/metabolism*
		                        			;
		                        		
		                        			Seedlings/metabolism*
		                        			
		                        		
		                        	
6.Clinical study of the oxygen drive aerosol inhalation with budesonide and ambroxol in the prevention of adult post-thoracotomy pneumonia.
Gang LI ; Jian Sheng WANG ; Si Da QIN ; Jia ZHANG ; Ning DU ; Jing ZHANG ; Xin SUN ; Hong REN
Journal of Peking University(Health Sciences) 2018;50(5):840-844
		                        		
		                        			OBJECTIVE:
		                        			To study the clinical effect of the oxygen drive aerosol in halation with budesonide and ambroxol in the prevention of adult post-thoracotomy pneumonia.
		                        		
		                        			METHODS:
		                        			This was a randomized, open and parallel controlled trial. We chose 80 cases of patients in the department of thoracic surgery in the First Affiliated Hospital of Xi'an Jiaotong University which fitted our criteria as the research object. The selected patients were randomly divided into the active group and the control group, and the active group underwent oxygen drive aerosol inhalation (2 mg budesonide combined 60 mg ambroxol) for 3 days before operation, and the control group without preoperative aerosol inhalation, and their postoperative therapy was the same.
		                        		
		                        			RESULTS:
		                        			The baseline data showed that the differences in sex, age, disease and smoking were not statistically significant between the two groups, P>0.05. The results of blood gas analysis before 12 hours of operation suggested that, the PaO₂and PaCO₂values of the active group were (88.40±9.40) mmHg and (38.30±6.10) mmHg; The PaO₂and PaCO₂ values of the control group were (85.09±7.18) mmHg and (41.21±3.15) mmHg. And the two groups' P values were 0.029 and 0.011, with statistical differences. There were 3 patients who developed postoperative pneumonia out of 40 patients in the active group, the incidence was 7.50%, but the incidence of control group was 25.00%. The P value was 0.034, with statistical differences. We also analyzed the influence of different diseases and surgical methods on postoperative pneumonia, and the results showed that in the active group and the control group, the incidence of postoperative pneumonia in the patients with esophageal cancer was lower than that in lung cancer patients, and there was a statistically significant difference (P<0.05). In the active group, the numbers of pulmonary deed resection, lobectomy and pulmonary sleeve resection were 2, 21 and 1 cases respectively, and the corresponding numbers in the control group were 2, 21 and 2. Among the two groups, the incidence of postoperative pneumonia in the patients with different surgical methods of lung cancer was statistically significant (P<0.05).
		                        		
		                        			CONCLUSION
		                        			If we implement respiratory preparation with budesonide plus ambroxol inhalation for 3 days before operation, we can greatly reduce the incidence of postoperative pneumonia?
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Aerosols
		                        			;
		                        		
		                        			Ambroxol/administration & dosage*
		                        			;
		                        		
		                        			Bronchodilator Agents/administration & dosage*
		                        			;
		                        		
		                        			Budesonide/administration & dosage*
		                        			;
		                        		
		                        			Drug Therapy, Combination
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Oxygen
		                        			;
		                        		
		                        			Pneumonia/prevention & control*
		                        			;
		                        		
		                        			Thoracotomy/adverse effects*
		                        			
		                        		
		                        	
7.A Case of a Herbicide Poisoning Induced Methemoglobinemia Patient Treated with High-dose Vitamin C.
Kyung Hoon SUN ; Jun Kew KIM ; Chang Yeon RYU ; Seo Jin KIM ; Hyeon Kyu JO ; Tae Ho YOO ; Yong Jin PARK ; Sun Pyo KIM
Journal of The Korean Society of Clinical Toxicology 2017;15(2):148-151
		                        		
		                        			
		                        			Methemoglobinemia is a condition in which the iron portion of hemoglobin, which binds to oxygen, is oxidized to produce methemoglobin, which increases blood concentration. There are many causes of methemoglobinemia, the most common being food, drugs, and chemicals. A 75-year-old male patient who had taken an herbicide did not notice any nonspecific symptoms. However, after 4 hours, his methemoglobin levels increased to 17.1%, while after 7 hours it increased to 26.5%, at which time intravenous administration of methylene blue 1 mg/kg (an antidote) was started. After a total of five doses of methylene blue at 1 mg/kg due to reactive methemoglobinemia for about 36 hours, the methemoglobin levels increased to 23.7%. Because no more methylene blue could be administered, 10 g of ascorbic acid (vitamin C) was administered intravenously. After 82 hours, ascorbic acid 10 g was administered six times for repeated reactive methemoglobinemia. No additional reactive methemoglobinemia was observed. The ventilator and endotracheal tube were successfully removed on day 5 after admission.
		                        		
		                        		
		                        		
		                        			Administration, Intravenous
		                        			;
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Ascorbic Acid*
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Iron
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Methemoglobin
		                        			;
		                        		
		                        			Methemoglobinemia*
		                        			;
		                        		
		                        			Methylene Blue
		                        			;
		                        		
		                        			Oxygen
		                        			;
		                        		
		                        			Poisoning*
		                        			;
		                        		
		                        			Ventilators, Mechanical
		                        			;
		                        		
		                        			Vitamins*
		                        			
		                        		
		                        	
8.Intravenous administration of piceatannol, an arginase inhibitor, improves endothelial dysfunction in aged mice.
Minh Cong NGUYEN ; Sungwoo RYOO
The Korean Journal of Physiology and Pharmacology 2017;21(1):83-90
		                        		
		                        			
		                        			Advanced age is one of the risk factors for vascular diseases that are mainly caused by impaired nitric oxide (NO) production. It has been demonstrated that endothelial arginase constrains the activity of endothelial nitric oxide synthase (eNOS) and limits NO generation. Hence, arginase inhibition is suggested to be vasoprotective in aging. In this study, we examined the effects of intravenous injection of Piceatannol, an arginase inhibitor, on aged mice. Our results show that Piceatannol administration reduced the blood pressure in aged mice by inhibiting arginase activity, which was associated with NO production and reactive oxygen species generation. In addition, Piceatannol administration recovered Ca²⁺/calmodulin-dependent protein kinase II phosphorylation, eNOS phosphorylation and eNOS dimer stability in the aged mice. The improved NO signaling was shown to be effective in attenuating the phenylephrine-dependent contractile response and in enhancing the acetylcholine-dependent vasorelaxation response in aortic rings from the aged mice. These data suggest Piceatannol as a potential treatment for vascular disease.
		                        		
		                        		
		                        		
		                        			Administration, Intravenous*
		                        			;
		                        		
		                        			Aging
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Arginase*
		                        			;
		                        		
		                        			Blood Pressure
		                        			;
		                        		
		                        			Injections, Intravenous
		                        			;
		                        		
		                        			Mice*
		                        			;
		                        		
		                        			Nitric Oxide
		                        			;
		                        		
		                        			Nitric Oxide Synthase Type III
		                        			;
		                        		
		                        			Phosphorylation
		                        			;
		                        		
		                        			Protein Kinases
		                        			;
		                        		
		                        			Reactive Oxygen Species
		                        			;
		                        		
		                        			Risk Factors
		                        			;
		                        		
		                        			Vascular Diseases
		                        			;
		                        		
		                        			Vasodilation
		                        			
		                        		
		                        	
9.Value of non-sexual penile erection for penile rehabilitation in men with erectile dysfunction.
Bo-Dong LÜ ; Wen-Zhi WANG ; Jun-Feng YAN ; Gao-Yue ZHANG
National Journal of Andrology 2017;23(8):675-679
		                        		
		                        			
		                        			Erectile dysfunction (ED) is a common male disease. Some related studies show that the prevalence of ED is nearly 52% in men aged 40 to 70 years and is increasing among younger males. Hypoxia is now considered to be an independent risk factor for ED and the mechanisms of hypoxia inducing ED are varied and complicated. Recently, an idea in penile rehabilitation has attracted much attention, which aims at improving erectile function by increasing oxygen supply to the cavernosum and reducing tissue fibrosis and apoptosis. The approaches to achieve non-sexual penile erection by increasing oxygen supply to the cavernosum, such as behavior therapy, medication, vacuum constriction device, and intracavernous injection, can simulate normal sexual erection and help patients with penile rehabilitation. This review focuses on the strategies for non-sexual penile erection in penile rehabilitation.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Erectile Dysfunction
		                        			;
		                        		
		                        			epidemiology
		                        			;
		                        		
		                        			etiology
		                        			;
		                        		
		                        			rehabilitation
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Hypoxia
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			therapy
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Oxygen
		                        			;
		                        		
		                        			administration & dosage
		                        			;
		                        		
		                        			Penile Erection
		                        			;
		                        		
		                        			Penis
		                        			;
		                        		
		                        			blood supply
		                        			;
		                        		
		                        			Risk Factors
		                        			
		                        		
		                        	
10.Vascular protective effects of aqueous extracts of Tribulus terrestris on hypertensive endothelial injury.
Yue-Hua JIANG ; Jin-Hao GUO ; Sai WU ; Chuan-Hua YANG
Chinese Journal of Natural Medicines (English Ed.) 2017;15(8):606-614
		                        		
		                        			
		                        			Angiotensin II (Ang II) is involved in endothelium injury during the development of hypertension. Tribulus terrestris (TT) is used to treat hypertension, arteriosclerosis, and post-stroke syndrome in China. The present study aimed to determine the effects of aqueous TT extracts on endothelial injury in spontaneously hypertensive rats (SHRs) and its protective effects against Ang II-induced injury in human umbilical vein endothelial cells (HUVECs). SHRs were administered intragastrically with TT (17.2 or 8.6 g·kg·d) for 6 weeks, using valsartan (13.5 mg·kg·d) as positive control. Blood pressure, heart rate, endothelial morphology of the thoracic aorta, serum levels of Ang II, endothelin-1 (ET-1), superoxide dismutase (SOD) and malonaldehyde (MDA) were measured. The endothelial injury of HUVECs was induced by 2 × 10 mol·L Ang II. Cell Apoptosisapoptosis, intracellular reactive oxygen species (ROS) was assessed. Endothelial nitric oxide synthase (eNOS), ET-1, SOD, and MDA in the cell culture supernatant and cell migration were assayed. The expression of hypertension-linked genes and proteins were analyzed. TT decreased systolic pressure, diastolic pressure, mean arterial pressure and heart rate, improved endothelial integrity of thoracic aorta, and decreased serum leptin, Ang II, ET-1, NPY, and Hcy, while increased NO in SHRs. TT suppressed Ang II-induced HUVEC proliferation and apoptosis and prolonged the survival, and increased cell migration. TT regulated the ROS, and decreased mRNA expression of Akt1, JAK2, PI3Kα, Erk2, FAK, and NF-κB p65 and protein expression of Erk2, FAK, and NF-κB p65. In conclusion, TT demonstrated anti-hypertensive and endothelial protective effects by regulating Erk2, FAK and NF-κB p65.
		                        		
		                        		
		                        		
		                        			Angiotensin II
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Antihypertensive Agents
		                        			;
		                        		
		                        			administration & dosage
		                        			;
		                        		
		                        			Apoptosis
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			Blood Pressure
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			Endothelium, Vascular
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Human Umbilical Vein Endothelial Cells
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Hypertension
		                        			;
		                        		
		                        			drug therapy
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			physiopathology
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			NF-kappa B
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Nitric Oxide Synthase Type III
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Oxidative Stress
		                        			;
		                        		
		                        			drug effects
		                        			;
		                        		
		                        			Plant Extracts
		                        			;
		                        		
		                        			administration & dosage
		                        			;
		                        		
		                        			Proto-Oncogene Proteins c-akt
		                        			;
		                        		
		                        			genetics
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Rats
		                        			;
		                        		
		                        			Rats, Inbred SHR
		                        			;
		                        		
		                        			Rats, Inbred WKY
		                        			;
		                        		
		                        			Reactive Oxygen Species
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Tribulus
		                        			;
		                        		
		                        			chemistry
		                        			
		                        		
		                        	
            
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