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1.
Clin Nutr ESPEN ; 33: 39-41, 2019 10.
Article in English | MEDLINE | ID: mdl-31451273

ABSTRACT

BACKGROUND & AIMS: Consumption of sugars in food and beverages has increased at an alarming rate. While excessive daily sugar intake has been well-associated as the onset of medical complications, additional sugars are still used in manufactured food products just to satisfy the consumers' needs. Hence, there is a need to develop sugar replacers that have low glycemic response without compromising the organoleptic characteristics of food products. This study aimed to determine if SUITENA™, a novel sweetener containing erythritol, xylitol, and Stevia, has low glycemic response upon consumption by human subjects. METHODS: Six human subjects were randomly chosen and were healthy at the point of experimentation. Capillary blood was collected via finger-prick method to monitor the glycemic response of every individual for 90 min after ingestion of sugar solution. RESULTS: It was found that the mean area under the curve (AUC) of the dextrose standard was 11.8-fold higher (p < 0.05) than the AUC of SUITENA™. SUITENA™ was not able to increase blood glucose level for up to 90 min while a spike in blood glucose level was observed from 15 min post-consumption of dextrose solution. We found that SUITENA™ has elicited a glycemic response 8% relative to the standard. Such low glycemic response has been reported by studies on other novel sugars. CONCLUSION: This preliminary finding suggested that SUITENA™ is a healthier alternative to fast sugars due to its low glycemic response. A larger sampling size is required to confirm the results.


Subject(s)
Glycemic Index , Polymers/administration & dosage , Research Subjects , Stevia/chemistry , Sugars/administration & dosage , Sweetening Agents/administration & dosage , Beverages , Blood Glucose , Diterpenes, Kaurane , Ethics , Food , Glucose , Glucosides , Humans , Malaysia , Plant Extracts , Single-Blind Method
2.
Neuropeptides ; 61: 87-93, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27823858

ABSTRACT

Germline deletion of the Prader-Willi syndrome (PWS) candidate gene Snord116 in mice leads to some classical symptoms of human PWS, notably reductions in body weight, linear growth and bone mass. However, Snord116 deficient mice (Snord116-/-) do not develop an obese phenotype despite their increased food intake and the underlying mechanism for that is unknown. We tested the phenotypes of germline Snord116-/- as well as neuropeptide Y (NPY) neuron specific Snord116lox/lox/NPYcre/+ mice at 30°C, the thermoneutral temperature of mice, and compared these to previous reports studies conducted at normal room temperature. Snord116-/- mice at 30°C still weighed less than wild type but had increased body weight gain. Importantly, food intake and energy expenditure were no longer different at 30°C, and the reduced bone mass and nasal-anal length observed in Snord116-/- mice at room temperature were also normalized. Mechanistically, the thermoneutral condition led to the correction of the mRNA expression of NPY and pro-opiomelanocortin (POMC), which were both previously observed to be significantly up-regulated at room temperature. Importantly, almost identical phenotypes and NPY/POMC mRNA expression alterations were also observed in Snord116lox/lox/NPYcre/+ mice, which lack the Snord116 gene only in NPY neurons. These data illustrate that mild cold stress is a critical factor preventing the development of obesity in Snord116-/- mice via the NPY system. Our study highlights that the function of Snord116 in the hypothalamus may be to enhance energy expenditure, likely via the NPY system, and also indicates that Snord116 function in mice is strongly dependent on environmental conditions such as cold exposure.


Subject(s)
Energy Metabolism/genetics , Homeostasis/genetics , Neurons/metabolism , Prader-Willi Syndrome/genetics , RNA, Small Nucleolar/genetics , Animals , Body Weight/genetics , Eating/genetics , Hypothalamus/metabolism , Mice , Mice, Knockout , Neuropeptide Y/genetics , Neuropeptide Y/metabolism , Prader-Willi Syndrome/metabolism , Pro-Opiomelanocortin/genetics , Pro-Opiomelanocortin/metabolism , RNA, Small Nucleolar/metabolism , Temperature
3.
J Laryngol Otol ; 124(5): 529-32, 2010 May.
Article in English | MEDLINE | ID: mdl-20163747

ABSTRACT

OBJECTIVE: To determine the prevalence and profile of patients who use complementary and alternative medicine, within a cohort of head and neck cancer patients. STUDY DESIGN: Cross-sectional survey. SUBJECTS AND METHODS: Ninety-three consecutive head and neck cancer patients being followed up at the department of otolaryngology head and neck surgery were surveyed using an interviewer-administered questionnaire. RESULTS: The prevalence of complementary and alternative medicine use was 67.8 per cent. Patients who used complementary and alternative medicine were more likely to be female, better educated and younger, compared with non-users. A total of 82.5 per cent (52/63) perceived complementary and alternative medicine to be effective, even though they were aware of the lack of research and endorsement by their physician regarding such medicine. CONCLUSION: The use of complementary and alternative medicine by head and neck cancer patients is common, regardless of efficacy or cost. Clinicians should routinely ask patients about their use of complementary and alternative medicine, to facilitate communication and enable appropriate use of such medicine.


Subject(s)
Complementary Therapies/statistics & numerical data , Head and Neck Neoplasms/therapy , Adolescent , Adult , Age Factors , Aged , Aged, 80 and over , Complementary Therapies/methods , Cross-Sectional Studies , Educational Status , Female , Humans , Male , Middle Aged , Sex Factors , Singapore , Young Adult
4.
Int J Stroke ; 2(2): 144-50, 2007 May.
Article in English | MEDLINE | ID: mdl-18705976

ABSTRACT

BACKGROUND: Epidemiological studies suggest that raised plasma concentrations of total homocysteine (tHcy) may be a common, causal and treatable risk factor for atherothromboembolic ischaemic stroke, dementia and depression. Although tHcy can be lowered effectively with small doses of folic acid, vitamin B(12) and vitamin B(6), it is not known whether lowering tHcy, by means of B vitamin therapy, can prevent stroke and other major atherothromboembolic vascular events. AIM: To determine whether the addition of B-vitamin supplements (folic acid 2 mg, B(6) 25 mg, B(12) 500 microg) to best medical and surgical management will reduce the combined incidence of stroke, myocardial infarction (MI) and vascular death in patients with recent stroke or transient ischaemic attack (TIA) of the brain or eye. DESIGN: A prospective, international, multicentre, randomised, double blind, placebo-controlled clinical trial. SETTING: One hundred and four medical centres in 20 countries on five continents. SUBJECTS: Eight thousand (6600 recruited as of 5 January, 2006) patients with recent (<7 months) stroke (ischaemic or haemorrhagic) or TIA (brain or eye). RANDOMISATION: Randomisation and data collection are performed by means of a central telephone service or secure internet site. INTERVENTION: One tablet daily of either placebo or B vitamins (folic acid 2 mg, B(6) 25 mg, B(12) 500 mug). PRIMARY OUTCOME: The composite of stroke, MI or death from any vascular cause, whichever occurs first. Outcome and serious adverse events are adjudicated blinded to treatment allocation. SECONDARY OUTCOMES: TIA, unstable angina, revascularisation procedures, dementia, depression. STATISTICAL POWER: With 8000 patients followed up for a median of 2 years and an annual incidence of the primary outcome of 8% among patients assigned placebo, the study will have at least 80% power to detect a relative reduction of 15% in the incidence of the primary outcome among patients assigned B vitamins (to 6.8%/year), applying a two-tailed level of significance of 5%. CONCLUSION: VITATOPS aims to recruit and follow-up 8000 patients between 1998 and 2008, and provide a reliable estimate of the safety and effectiveness of folic acid, vitamin B(12), and vitamin B(6) supplementation in reducing recurrent serious vascular events among a wide range of patients with TIA and stroke throughout the world.


Subject(s)
Ischemic Attack, Transient/prevention & control , Research Design , Stroke/prevention & control , Vitamin B Complex/therapeutic use , Humans , Secondary Prevention
5.
Neurosci Lett ; 398(1-2): 28-33, 2006 May 01.
Article in English | MEDLINE | ID: mdl-16443325

ABSTRACT

It has been well documented that oxidative stress is involved in stroke. Currently, many neuroprotective strategies have been targeted at molecules that are able to act as an oxidant to intervene with free-radical mediated apoptosis in the ischemic penumbra. In particular, natural products which contain antioxidant properties have undoubtedly efficacious for stroke treatment. In the current study, therapeutic effects of Ginkgo biloba extract (EGb) against cerebral protection in Wistar rats underwent middle cerebral artery occlusion (MCAO) was evaluated. A comparison study was conducted by using Losartan, an antihypertensive drug. Gene expression levels of pro-apoptotic genes (AT2 receptor, Fas, Bax and Bcl-xS) have shown to have significant reduction by EGb- and Losartan-treated groups as compared to vehicle group. Significant reduction of immunoreactivity of protein production of these genes, together with least nuclear green fluorescence observed in TUNEL, EGb, as an antioxidant drug, is concluded to have potent and promising therapeutic effect for stroke treatment.


Subject(s)
Angiotensin II Type 1 Receptor Blockers/therapeutic use , Antioxidants/therapeutic use , Cerebral Cortex/drug effects , Ginkgo biloba , Losartan/therapeutic use , Stroke/prevention & control , Animals , Apoptosis , Cerebral Cortex/metabolism , Cerebral Cortex/pathology , Immunohistochemistry , In Situ Nick-End Labeling , Infarction, Middle Cerebral Artery/metabolism , Infarction, Middle Cerebral Artery/pathology , Infarction, Middle Cerebral Artery/prevention & control , Male , Phytotherapy , Plant Extracts/therapeutic use , Rats , Rats, Wistar , Receptor, Angiotensin, Type 2/biosynthesis , Reverse Transcriptase Polymerase Chain Reaction , Stroke/metabolism , Stroke/pathology , bcl-2-Associated X Protein/biosynthesis , bcl-X Protein/biosynthesis , fas Receptor/biosynthesis
6.
Singapore Med J ; 46(2): 88-9, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15678291

ABSTRACT

A 35-year-old Chinese man presented with acute thyrotoxic periodic paralysis complicated by near-fatal cardiac arrhythmias due to persistent hypokalaemia, despite maximum potassium supplementation. He was eventually resuscitated with external cadioversion. In this unusual case of severe refractory hypokalaemia leading to ventricular fibrillation in a patient with underlying thyrotoxicosis, the potential dangers concerning the use of dextrose infusion and beta-adrenergic agent for resuscitation are highlighted.


Subject(s)
Hypokalemic Periodic Paralysis/etiology , Thyrotoxicosis/complications , Ventricular Fibrillation/etiology , Adult , Antithyroid Agents/administration & dosage , Glucose/adverse effects , Humans , Hypokalemic Periodic Paralysis/drug therapy , Male , Propylthiouracil/administration & dosage , Sweetening Agents/adverse effects , Thyrotoxicosis/drug therapy , Ventricular Fibrillation/drug therapy
7.
Cerebrovasc Dis ; 19(2): 110-6, 2005.
Article in English | MEDLINE | ID: mdl-15608435

ABSTRACT

BACKGROUND AND AIMS: It is uncertain what impact increasing voluntary folate fortification may be having on the statistical power of randomized trials testing the homocysteine hypothesis of atherothrombosis. The objective of this study was to determine whether there has been a change in folate status between 1998 and 2002 in stroke patients randomized into the VITAmins TO Prevent Stroke (VITATOPS) Study at a single center in Perth, Australia, and what impact this may have had on the magnitude of the homocysteine-lowering effect achieved over time with folic acid-based multivitamin therapy. METHODS: We conducted a randomized, double-blind, placebo-controlled study involving 285 patients with stroke or transient ischemic attack who were recruited between 1998 and 2002 and randomized to long-term folic acid 2.0 mg/day, pyridoxine 25 mg/day and cobalamin 0.5 mg/day (active VITATOPS medication) or placebo. Fasting plasma total homocysteine, red cell folate, serum cobalamin and serum pyridoxine levels were measured at baseline and 6 months, and the change in blood levels over 4 time quartiles and differences in levels between the two randomized treatments were examined. RESULTS: Between 1998 and 2002, there was a significant rise in baseline mean red cell folate levels over 4 time quartiles among the entire stroke cohort (723.3, 780.1, 922.6 and 1,023.7 nmol/l in the first, second, third and fourth quartiles, respectively; p < 0.0001), but this was not associated with a spontaneous reduction in mean baseline total homocysteine levels during the same time period (12.7, 14.3, 12.1 and 12.8 micromol/l in the first, second, third and fourth quartiles, respectively; p = 0.55). The homocysteine-lowering effect of the active VITATOPS trial medication at 6 months after randomization also did not change significantly between 1998 and 2002 (difference between randomized groups: -4.1, -4.1, -3.1 and -3.6 micromol/l in the first, second, third and fourth quartiles, respectively; p = 0.56). CONCLUSIONS: The homocysteine-lowering effect of the active VITATOPS trial medication has not attenuated significantly in the past 5 years despite increasing voluntary fortification of foods with folic acid as reflected by a progressive rise in baseline folate status. These data suggest that in the continuing absence of a program of mandatory folate fortification of food in populations served by centers participating in the VITATOPS trial, the study will remain adequately powered to test the homocysteine-lowering hypothesis for which it was designed.


Subject(s)
Folic Acid/blood , Homocysteine/blood , Homocysteine/drug effects , Pyridoxine/blood , Stroke/blood , Vitamin B 12/blood , Aged , Dietary Supplements , Female , Folic Acid/pharmacology , Follow-Up Studies , Hematinics/blood , Hematinics/pharmacology , Humans , Male , Middle Aged , Pyridoxine/pharmacology , Time Factors , Vitamin B 12/pharmacology
9.
Singapore Med J ; 42(3): 115-6, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11405562

ABSTRACT

We present a case of a man who developed gynaecomastia after ingestion of "Dong Quai" pills. "Dong Quai" is the Chinese name for the herb Angelica polymorpha var. sinensis which is widely used as a panacea for gynaecological problems, and it is also proclaimed as an invigorating tonic for both women and men. The pharmacological effects of "Dong Quai" are likely related to the phytoestrogen that it contains. This report highlights the potential adverse effects associated with its consumption in the male, especially for the processed "Dong Quai" pills which may contain significantly higher levels of phytoestrogen than its original herbal product.


Subject(s)
Drugs, Chinese Herbal/adverse effects , Gynecomastia/etiology , Adult , Angelica sinensis , Drugs, Chinese Herbal/therapeutic use , Gonadal Steroid Hormones/blood , Humans , Male , Medicine, Chinese Traditional
10.
Cancer Treat Rep ; 68(2): 409-10, 1984 Feb.
Article in English | MEDLINE | ID: mdl-6607770

ABSTRACT

Twenty-six evaluable patients with advanced soft tissue and bony sarcomas refractory to chemotherapy were treated with vincristine plus high-dose methotrexate and leucovorin rescue. A 14% response rate was observed among 14 patients presenting with refractory soft tissue sarcomas. No responses were observed among 12 patients with bony sarcoma. Toxic reaction with nausea, vomiting, nephrotoxicity, and myelosuppression was manageable. While this study did demonstrate activity of this regimen in doxorubicin-refractory patients, the duration of the responses was relatively brief. Thus, the clinical utility of such a regimen is questionable.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Methotrexate/administration & dosage , Sarcoma/drug therapy , Bone Neoplasms/drug therapy , Dose-Response Relationship, Drug , Drug Evaluation , Humans , Leucovorin/administration & dosage , Lung Neoplasms/drug therapy , Lung Neoplasms/secondary , Vincristine/administration & dosage
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