1.Comparison of Nutritional Qualities and Antioxidant Properties of Ready–to-Eat Fruit-Enriched Corn Based Breakfast Cereals
Malaysian Journal of Nutrition 2012;18(3):373-382
Introduction: The study aimed to analyse the nutritional quality, antioxidant components and activity of three varieties of corn based ready-to- eat (RTE)
breakfast cereals (BFC) enriched with strawberry, banana and mango. Methods: Fruit-enriched corn based breakfast cereals manufactured in India were purchased and ground to obtain homogeneous samples for analysis. The contents of
moisture, protein, total fat, dietary fibre, iron, phosphorous, calcium, vitamin C, total carotene, thiamine, riboflavin, in vitro digestible protein, bioaccessible
calcium and iron, and digestible starch fractions were determined. The antioxidant components namely, polyphenols, flavonoids and antioxidant activity in different extracts were also determined using total antioxidant, free radical scavenging(2,2-diphenyl-1-picrylhydrazyl) and reducing power assays. Results: The protein and dietary fibre contents in all samples ranged between 4.0-4.6 and 6.4-7.6 g/100g respectively. Total iron and vitamin C ranged between 10.7-13.3 mg and
33.2-43.6 mg/100g respectively. Cereals with mango had high total carotene in comparison with other samples. In vitro digestible protein of the processed cereals
was low, while bioaccessible calcium (50.2-59.5%) and iron (8.5-15.1%) levels were high due to low oxalates and phytic acid contents. The starch profiles of the
breakfast cereals showed high rapidly available glucose and starch digestibility index. Fruit-enriched breakfast cereals showed high polyphenol content in
methanol extract (48.6-71.3 mg/100g) and high total antioxidant activity in aqueous extracts. Free radical scavenging and reducing power assay showed
high activity in 80% methanol extract. Conclusion: Fruit-enriched breakfast cereals have the potential to be a good source of iron, dietary fibre, vitamin C and total carotene. The fruit-enriched cereals also had high bioaccessible iron and antioxidant activity.
2.The Causal Relationship Between Infant Mortality Rate, Health Expenditure And Economic Growth In India
Prakash R. Kengnal ; Sharankumar Holyachi
International Journal of Public Health Research 2017;7(1):799-806
The Infant Mortality Rate defined as the risk for a live born child to die before its first birthday, is known to be one of the most sensitive and commonly used indicators of the social and economic development of a nation. This paper investigates the causal relationship between infant mortality rate, economic growth and private health expenditure [% Gross Domestic Product (GDP)] in India using the co-integration and Granger causality frameworks for the period from 1995 to 2013 using secondary data from various sources. We have examined the presence of a long-run equilibrium relationship using the bounds testing approach to co-integration within the Unrestricted Error- Correction Model (UECM). We have also examined the direction of causality between infant mortality rate, economic growth and private health expenditure (% GDP) in India using the Granger causality test within the Vector Error-Correction Model (VECM). As a summary of the empirical findings, we find the Infant Mortality Rate (IMR), Per-Capita Gross Domestic Product (PCGDP) and private health expenditure (% GDP) are co-integrated. The results of Granger Causality suggested that no short-run effect was existing between all the three variables. The error-correction term implies that the variable is non-explosive and long-run equilibrium relationship is attainable.
3.Antidiabetic and hypolipidemic activities of Dillenia indica extract in diabetic rats.
Sunil KUMAR ; Vipin KUMAR ; Om PRAKASH
Journal of Integrative Medicine 2011;9(5):570-4
Objective: The present study was carried out to investigate the antidiabetic and hypolipidemic activities of bioactive fraction (ethyl acetate fraction) of Dillenia indica methanolic extract in experimental diabetic Wistar rats. Methods: Type-1 diabetes was induced by single intraperitoneal injection of streptozotocin (60 mg/kg body weight), and type-2 diabetes was induced by single intraperitoneal injection of streptozotocin (60 mg/kg body weight), 15 min after the intraperitoneal injection of 120 mg/kg nicotinamide. The rats were treated by administering graded oral doses of isolated ethyl acetate fraction of methanolic extract of D. indica (DIEE), 200 and 400 mg/kg body weight, respectively, for 21 d. The blood glucose level was estimated at weekly intervals by glucometer. Serum cholesterol, triglycerides and high-density lipoprotein cholesterol (HDL-C) were also evaluated in normal and diabetic rats by an autoanalyzer. Results: In both experimental models, daily oral treatment with DIEE for 21 d resulted in a significant reduction in blood glucose (P<0.01), serum cholesterol (P<0.05) and triglycerides (P<0.05) levels whereas HDL-C level was found to be increased (P<0.05) as compared with the diabetic control group. Conclusion: DIEE at 400 mg/kg body weight has prominent antidiabetic effect in experimental type-1 and type-2 diabetes models in rats. It may therefore be used as an alternative remedy for the treatment of diabetes mellitus.
4.Antimicrobial activity of certain fresh water microalgae from Thamirabarani River, Tamil Nadu, South India
Prakash Wilfred Justella ; MarimuthuAntonisamy Johnson ; Jeeva Solomon
Asian Pacific Journal of Tropical Biomedicine 2011;(z2):170-173
Objective:To evaluate the antimicrobial potential of fresh water microalgae viz., Oscillatoria sancta (O. sancta) (Kuetz) Gomont., Lyngbya birgei (L. birgei) Smith G.M., Oedogonium echinospermum (O. echinospermum), Spirogyra decimina (S. decimina) (Muller) Kuetz., Spirogyra grantiana (S. grantiana) Transeau., Spirogyra crassa (S. crassa), Spirogyra biformis (S. biformis) Jao. and Spirogyra condensata (Vaucher) Kuetz against human bacterial pathogens. Methods:Antimicrobial study was carried out by disc diffusion method against the pathogens viz., Escherichia coli (E. coli) (ATCC 35218), Staphylococcus aureus (S. aureus) (ATCC 6538), Salmonella typhi (S. typhi) (MTCC 733), Proteus vulgaris (P. vulgaris), Proteus mirabilis (P. mirabilis) and Streptococcus pyogenes. Results: The methanolic extract of O. sancta showed the antibacterial activity against three pathogens viz., P. mirabilis, P. vulgaris and S. aureus with the inhibition zones of 10, 8 and 8 mm, respectively. The methanolic and ethanolic extracts of L. birgei exhibited the antibacterial activity against two pathogens i.e. P. mirabilis and P. vulgaris with the maximum zone of inhibition of 8 and 8 mm, respectively. The ethanolic extracts of O. echinospermum displayed the antibacterial activity against S. typhi and P. mirabilis with the maximum of zone of inhibition (7 mm). The methanolic extracts of S. decimina exhibited the antibacterial activity against S. aureus and P. mirabilis with the maximum zone of inhibition of 12 and 9 mm, respectively. The ethanolic extracts of S. grantiana showed the anti-bacterial activity against three organisms i.e. E. coli, P. vulgaris and P. mirabilis with the zone of inhibition of 9, 10 and 9 mm, respectively. The methanolic extracts of S. crassa exhibited the antibacterial activity against P. mirabilis with the maximum zone of inhibition (9 mm). The methanolic extracts of S. biformis exhibited the antibacterial activity against P. vulgaris with the maximum zone of inhibition (8 mm). Conclusions: These results give an indication of the presence of promising antibacterial compounds in the plants under studied. Further phytochemical studies are needed to elucidate the components responsible for antibacterial activity of these extracts against bacteria.
5.Pharmacognostic evaluation of stem bark of Pongamia pinnata (L.) Pierre
Dinesh KUMAR ; Ajay KUMAR ; Om PRAKASH
Asian Pacific Journal of Tropical Biomedicine 2012;(z2):543-546
Objective: To perform the pharmacognostic study of Pongamia pinnata (L.) Pierre (P. pinnata) stem bark. Method: The pharmacognostic studies were carried out in terms of organoleptic, macroscopic, microscopic, fluorescence analysis and physicochemical parameters. Results: The bark consisting of channelled, recurved, slightly quilled, usually 0.2-1 cm thick, lenticellate pieces with outer surface ash-grey to greyish-brown and internal surface yellowish-white to cream coloured having unpleasant odour and bitter taste. The main microscopic characterstics of the bark include phellem (5-20 or more layers of cork), phellogen (2-3 layered) followed by 10-15 layered phelloderm. Among other microscopic components were phloem parenchyma, phloem fibre and stone cells, traversed by wavy medullary rays. Further, physicochemical analysis of the bark power showed total ash, water soluble ash, acid insoluble ash and sulphated ash as 10.94, 1.96, 1.47 and 15.8 % w/w respectively. The alcohol and water soluble extractives values of the stem bark were 9.6 and 18.4 %w/w respectively. Conclusions: Various pharmacognostic characters observed in this study helps in botanical identification and standardization of P. pinnata L. in crude form.
6.An Ergonomic Approach For Designing A Seat For Fish Processing Workers
Prakash C. Dhara ; Pratibha Pradhan ; Mousumi Chatterjee
Malaysian Journal of Public Health Medicine 2016;Special Volume(1):14-21
The present study aimed to design a sitting stool for fish processing worker to reduce the postural stress during work. The study was conducted on 74 male and female fish processing workers selected randomly. The Musculoskeletal Disorder (MSD) of the subjects was assessed by the modified Nordic Questionnaire method. The body joint angles were measured by a digital goniometer. The results revealed that MSD was highly prevalent in lower back region in both male (78.57%) and female (93.47%) workers. The results of body joint angles suggested a high degree of forward bending during work. Efforts were made to design a sitting stool considering the human factors of the users to reduce the postural problems. The stool was designed by considering 5th and 95th percentile values of different anthropometric dimensions of the male and female workers. Paired comparison tests were employed to determine optimum dimensions of the stool for ensuring the compatibility of the physical characteristics of the stool with human body. From the results of paired comparison test and anthropometric characteristics of the users, physical dimensions of the sitting stool were settled for final designing. From the results, the height of the stool was determined separately for male and female workers. In the suggested design the height of the seat was 25cm for male and 20cm for female where the length and depth of the seat were 40cm and 32cm respectively for both sexes.A mechanical system was incorporated in the design so that the same stool could be used by the male and female workers. Subjective evaluation indicated that most of the subjects (>75%) rated the seat as good or very good. The joint angle study with suggested seat showed improved working posture.
7.Haemodialysis associated amyloidosis of the tongue: a case report6
Hans Prakash Sathasivama ; Lau Shin Hin
Archives of Orofacial Sciences 2013;8(2):65-68
Haemodialysis associated amyloidosis (HAA) is a complication of long-term haemodialysis caused by deposition of β2- microglobulin in tissues that most often presents clinically at osteoarticular sites. However, in very rare circumstances, patients do present initially with oral manifestations of HAA. In a normally functioning kidney, β2- microglobulin is cleared by glomerular filtration and is catabolized in the proximal tubules. This article describes a patient with oral manifestation of haemodialysis associated amyloidosis with an unusual presenting complaint of lingual dysaesthesia.
8.Effectiveness and safety of hydroxychloroquine compared to teneligliptin in uncontrolled T2DM patients as add-on therapy.
Amit KUMAR ; Akhouri Sukrit PRAKASH
Journal of the ASEAN Federation of Endocrine Societies 2019;34(1):87-91
OBJECTIVES: Hydroxychloroquine (HCQ) 400 mg is approved by the Drug Controller General of India (DCGI) and recommended by the Research Society for the Study of Diabetes in India (RSSDI) clinical practice recommendations 2017 as add-on therapy after metformin and sulfonylurea in Type 2 Diabetes (T2DM) patients. The aim of this observational study is to compare the efficacy and safety of hydroxychloroquine 400 mg and teneligliptin 20 mg when used as add-on therapy in Indian Type 2 DM patients who were inadequately controlled (HbA1c ?7.5%) with metformin 1000 mg and glimepiride 2 mg combination.
METHODOLOGY: This study is a prospective observational study to be conducted in 2 diabetic centres of Patna city between October 2017 and May 2018 involving 180 patients followed up for 6 months. One group (N=90) of patients received hydroxychloroquine 400 mg + metformin 1000 mg + glimepiride 2 mg, the other group (N=90) received teneligliptin 20 mg + metformin 1000 mg + glimepiride 2 mg. Efficacy was assessed by fasting blood glucose (FBG), post prandial blood glucose (PPBG) and glycated haemoglobin (HbA1c) reduction. Safety was evaluated by the number of hypoglycaemic events and changes in serum creatinine levels. Home based glucose monitoring was used to detect the hypoglycaemic events. Patients who had any type of retinopathy/maculopathy were excluded.
RESULTS: Mean age of entire population was 66 ± 8 years with mean 6 ± 2 years of DM with 102 males. Mean body weight was 71 ± 12 kg. Baseline HbA1c was 8.1 ± 0.3 in the hydroxychloroquine group and 8.2 ± 0.2 in the teneligliptin group.
At 24 weeks there were statistically significant reductions in mean HbA1c in the hydroxychloroquine group (1.1 ± 0.3) as compared to the teneligliptin group (0.82 ± 0.3) (P?0.001). The mean FBG and PPBG was 169 ± 18 mg/dl and 232 ± 18 mg/dl respectively in hydroxychloroquine group which was reduced to 121 ± 15 mg/dl and 161 ± 19 mg/dl at the end of 24 weeks. In the teneligliptin group, FBG and PPBG was 171 ± 16 mg/dl and 239 ± 21 mg/dl at baseline, which was reduced to 121 ± 15 mg/dl and 161 ± 19 mg/dl respectively in same period of time (P? 0.005). There were 4 incidences of hypoglycaemic events in the hydroxychloroquine group (4.4%) and 6 in the teneligliptin group (6.67%). No patients required medical assistance for hypoglycaemic events. There was no statistically significant change in body weight in both the groups. No marked changes in creatinine levels were found in patients in both the groups.
CONCLUSION: In conclusion, treatment with hydroxychloroquine 400 mg for 24 weeks reduces glycaemic parameters more aggressively than teneligliptin 20 mg in Indian type 2 diabetes patients.
Human ; Hydroxychloroquine
9.Formulation and evaluation of herbal antioxidant face cream of Nardostachys jatamansi collected from Indian Himalayan region
Mishra Prakash Abhay ; Saklani Sarla ; Milella Luigi ; Tiwari Priyanka
Asian Pacific Journal of Tropical Biomedicine 2014;(z2):679-682
Objective:To prepare and evaluate a herbal antioxidant face cream which is made by the ethanol extract of Nardostachys jatamansi (Valerianceae).
Methods: Antioxidant activity of ethanol extract was assessed by previously reported 2, 2-Diphenyl-1-picrylhydrazyl method. By discovering different types of formulations, such as oil in water, we were able to create several face creams respectively classified from F1 to F6, by incorporating different concentrations of stearic acid and acetyl alcohol. The evaluation of all formulations (F1 to F6) has been done by the analysis of different parameters like pH, viscosity, spread ability and stability.
Results: An ethanol fraction analyzed from a sample of Nardostachys jatamansi showed a significant antioxidant activity with an IC50 value of 58.39 μg/mL while for ascorbic acid the IC50 value was 46.68 μg/mL. Among the six formulations (F1-F6) F5 and F6 showed good spread ability, good consistency, homogeneity, appearance, pH;there is no proof of a separation phase and ease of removal. Also the formulations F5 and F6 showed no redness or edema or erythema and irritation during irritancy studies.
Conclusions:These formulations can be safely used on the skin. Hence, the study suggests that the composition of extract and the base of the cream F5 and F6 are more stable and safe, but it may produce synergistic action.
10.A preliminary evaluation of comparative effectiveness of riluzole in therapeutic regimen for irritable bowel syndrome
Mishra Prakash Surya ; Shukla Kumar Sunit ; Pandey Lal Bajrang
Asian Pacific Journal of Tropical Biomedicine 2014;(z1):335-340
Objective: To develop agents that are specifically effective in controlling the key disturbance of visceral hyperalgesia besides abating of associated multiple symptoms, and evaluate comparative effectiveness for IBS symptom relief for standard regimen (antispasmodic and probiotic) and add-on amitriptyine or riluzole regimens following two weeks administration.Methods:groups were studied. First group received standard treatment (mebeverine 200 mg twice daily and probiotic 200 mg twice daily). Second group received add-on amitriptyline 25 mg before bedtime, while the third group got add-on riluzole 50 mg twice daily. Overall gastrointestinal symptom rating scale improving symptoms and hospital anxiety depression scale improving associated psychological morbidity were employed as measures at induction and at two-week follow-up period. Individual symptom scores were also examined to define the outcome profiles.Results:108 patients with visceral hypersensitivity accompanying IBS, divided into three rating scale score, not the other two regimens. Pain relief was seen with both riluzole and amitriptyline regimens significantly superior to standard treatment regimen, but riluzole effect appeared specific and independent anxiolytic effect. Amitriptyline caused relief in diarrhea and did not benefit in constipation point to non-specific remedial role in IBS. Riluzole regimen resulted in significant reduction of overall gastrointestinal symptom Conclusions: Riluzole specifically relieves visceral hypersensitivity and is proved to be superior to current treatments in IBS patients. It appears a lead remedy based on glutamate transporter mechanisms in visceral hypersensititvity.