Refine your search
Collections
Co-Authors
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
Venkatnarayanan, R.
- Acute and Subacute Toxicity study of Milnacipran Hydrochloride in Wistar rats by Oral Route
Abstract Views :295 |
PDF Views:0
Authors
D. Benito Johnson
1,
R. Suresh
1,
Prakash Rao Prathima
1,
R. Venkatnarayanan
1,
P. M. Ashir Ahammad
1
Affiliations
1 Department of Pharmacology, R.V.S. College of Pharmaceutical Sciences, Sulur, Coimbatore, Tamil Nadu, IN
1 Department of Pharmacology, R.V.S. College of Pharmaceutical Sciences, Sulur, Coimbatore, Tamil Nadu, IN
Source
Research Journal of Pharmacology and Pharmacodynamics, Vol 5, No 1 (2013), Pagination: 51-57Abstract
Toxicity of a substance is nothing but unwanted or series of adverse events that was initiated after administration of particular chemical, physical or biological agent. Acute toxicity study aim is to determine the occurred toxic manifestation of the administered test substance after expose to animals in one or more doses for a period of 14 days. The study provides the information or determination of therapeutic index, i.e. T.I. = LD50/ ED 50. Sub-acute toxicity testing evaluates the toxic effects of drug on repeated exposure and also provides the information on delayed and cumulative effect of the chemicals on the tissues or other biochemical mechanisms Depression is one of the most common psychiatric disorders. The symptoms of depression are often subtle and unrecognized both by patients and by physicians. Major depression remains difficult to treat, despite the wide array of registered antidepressant. Milnacipran is indicated for the treatment of major depressive disorder and management of fibromyalgia. Milnacipran inhibits norepinephrine and serotonin reuptake in a 3:1 ratio, in practical use this means a balanced (equal) action upon both transmitter.Keywords
Milancipran, Depression, Acute Toxicity, Sub-Acute ToxicityReferences
- Psychology and the National Institute of Mental Health: A Historical Analysis of Science, Practice, and Policy, Edited by Wade E. Pickren, PhD and Stanley F. Schneider, PhD, American Psychological Association, 2004.
- The sensitivity and specificity of the Major Depression Inventory, using the Present State Examination as the index of diagnostic validity… Journal of affective disorders, 66(2–3): 2001, 159–64.
- The internal and external validity of the Major Depression Inventory in measuring severity of depressive states... Psychological medicine, 33(2): 2003, 351– 356.
- Shaffer D, Gould MS, Fisher P, Trautman P, Moreau D, Kleinman M, Flory M, Psychiatric Diagnosis in Child and Adolescent Sucide. Archives of general psychiatry, 53(4): 1996, 339-348.
- March J, Silva S, Petrycki S, Curry J, Wells K, Fiarbank J, Burns B, Bomino M, Mcnulty S, Vitiello B, Severe J. Treatment for Adolescent with Depression Study (TADS) Team. Journal of the American Medical Association, 292(7): 2004, 807-820.
- HP Rang, MM Dale, JM Ritter, RJ Flower; RANG and DALE’s Pharmacology. 6thedition. New Delhi: Elsevier; P.557-574, 2007.
- The complete drug reference by Martindale (13th edition) Pharmaceutical press, Page no- 372-375,409, 2005.
- Hussam A. Yacoub, DO, MS, William G. Johnson, MD and Nizar Souayah, MD; Serotonin Syndrome After Administration of Milnacipran For Fibromyalgia; American Academy of Neurology; Neurology 23, 2010, Vol. 74.
- Moret C, Charveron M, Finberg JP, Couzinier JP, Briley M. "Biochemical profile of midalcipran (F 2207), 1-phenyl-1- diethyl-aminocarbonyl-2-aminomethyl-cyclopropane (Z) hydrochloride, a potential fourth generation antidepressant drug". Neuropharmacology 24 (12): 1985, 1211– 9.
- Briley M, Prost JF, Moret C. "Preclinical pharmacology of Milnacipran". International clinical psychopharmacology 11 Suppl 4: 1996. 9–14.
- R Michael Gendreau, Michael D Thorn, Judy F Gendreau, Jay D Kranzler; Efficacy of Milnacipran in patients with fibromyalgia, The Journal of Rheumatology ;Vol. 32 no. 10 , 2011, 1975-1985.
- Spencer C.M.; Wilde M.I; Milnacipran: A Review of its Use in Depression; Volume 56, Number 3, 1998, Page. 405-427(23).
- Mike Briley; Clinical experience with dual action antidepressants in different chronic pain syndromes; Human Psycho and Experimental Pharmacology; Article first published online: 20 SEP 2004, DOI: 10.1002/hup.621
- Anna M Redmond, John P Kelly, Brian E Leonard, The Determination of the Optimal Dose of Milnacipran in the Olfactory Bulbectomized Rat Model of Depression; Pharmacology Biochemistry and Behavior; Volume 62, Issue 4, April 1999, Pages 619–623.
- S.Neil Vaishnavi, Charles B Nemeroff, Susan J Plott, Srinivas G Rao, Jay Kranzler, Milnacipran: a comparative analysis of human monoamine uptake and transporter binding affinity; Biological Psychiatry; Volume 55, Issue 3, 1 February 2004, Pages 320–322.
- Wound Healing and Anti Bacterial Activity of the Leaves Extracts of Jasminum grandiflorum Linn
Abstract Views :243 |
PDF Views:1
Authors
T. Raja Sekharan
1,
M. Syam Mohan
2,
P. Natarajan
3,
A. S. William
3,
Arputha Sundar
3,
A. Thanga Thirupathi
3,
R. Venkatnarayanan
4
Affiliations
1 Department of Pharmaceutics , Sankaralingam Bhuvaneswari College of Pharmacy, Anaikuttam – 626 130, Sivakasi, Tamil Nadu, IN
2 UPM Makna Cancer Research Lab, Serdang - 43400, Selangor, MY
3 Sankaralingam Bhuvaneswari College of Pharmacy, Anaikuttam – 626 130, Sivakasi, Tamil Nadu, IN
4 RVS College of Pharmaceutical Sciences, Sulur, Coimbatore-641 402, Tamil Nadu, IN
1 Department of Pharmaceutics , Sankaralingam Bhuvaneswari College of Pharmacy, Anaikuttam – 626 130, Sivakasi, Tamil Nadu, IN
2 UPM Makna Cancer Research Lab, Serdang - 43400, Selangor, MY
3 Sankaralingam Bhuvaneswari College of Pharmacy, Anaikuttam – 626 130, Sivakasi, Tamil Nadu, IN
4 RVS College of Pharmaceutical Sciences, Sulur, Coimbatore-641 402, Tamil Nadu, IN
Source
Research Journal of Pharmacology and Pharmacodynamics, Vol 2, No 6 (2010), Pagination: 388-391Abstract
Petroleum ether, Chloroform, Ethanol and Aqueous extracts of Jasminum grandiflorum Linn leaves were tested for wound healing and antibacterial activity. Investigation were undertaken to screen the wound healing activity of different extracts of the leaves of Jasminum grandiflorum Linn on excision wound models in albino rats. The aqueous extracts shows significance wound healing activity when compared to the standard (Povidone iodine ointments). Other extract also shows wound healing activity but the wound contraction was less when compared to aqueous extracts and standard. For Salmonella typhi the zone of inhibition for petroleum ether extract is equal and for chloroform extract it is more active compared to that of the standard (Ciprofloxacin disc 5mcg/disc). Ethanolic extract is more active against Staphylococcus aureus than other microorganisms. Aqueous extract is more effective against Streptococcus pyogen and less active against Proteus when compared to the standard.Keywords
Jasminum Grandiflorum Linn; Antibacterial Activity, Wound Healing Activity.References
- Priya Joy and Patric Raja D. Anti-Bacterial Activity Studies of Jasminum grandiflorum and Jasminum sambac. Ethnobotanical Leaflets, 2008, 12: 481-483.
- Kulkarni PH and Ansari S. The Ayurvedic Plants: Indian Medical Science Series No. 132. Sri Satguru Publication, New Delhi, 2004,191.
- Sharma PC, Yelne MB and Dennis TJ. Database on Medicinal Plants Used in Ayurveda. CCRAS, New Delhi, 2005, 332-345.
- Brinda S, Ulla WS, George V, Pushpangadan P and Rajasekharan S. Angiotensin converting enzyme inhibitors from Jasminum azoricum and Jasminum grandiflorum, Planta Med, 1998, 64: 246-250.
- Sadhu SK, Khan MS, Ohtsuki T and Ishibashi M. Secoiridoids component from Jasminum grandiflorum, Phytochem, 2007, 68: 1718-21.
- Divakar NG, Subramanian V, Sugumaran M and Vaidyanathan CS. Indole oxygenase from the leaves of Jasminum grandiflorum, Plant Science Letter, 1979, 15: 177-180.
- Zhao GQ, Xia JJ and Dong JX. Glycosides from leaves of Jasminum grandiflorum var officinale, Acta Pharmaceutica Sinica, 2007, 42: 1066-9.
- Villegas LF, Fernandez ID, Maldonado H, Torres R, Zavaleta A, Vaisberg AJ and Hammond GB. Evaluation of the woundhealing activity of selected traditional medicinal plants from Peru. J Ethnopharmacol, 1997, 55: 193-200.
- Tsuchiya H Sato M, Miyazaki T, Fujiwara S, Tanigaki S, Ohyama M. et al. Comparative study on the antibacterial activity of phytochemical flavanones against methicillinresistant Staphylococcus aureus. J Ethnopharmacol, 1996, 50: 27-34.
- In Vivo Anti-Snake Venom Activity of Methanol Extract of Leaves of Orthosiphon stamineus in Mice
Abstract Views :274 |
PDF Views:0
Authors
Affiliations
1 Department of Pharmacology, R.V.S. College of Pharmaceutical Sciences, Sulur, Coimbatore-641402, Tamilnadu, IN
2 Department of Pharmacognosy, R.V.S. College of Pharmaceutical Sciences, Sulur, Coimbatore, Tamilnadu, IN
3 Department of Pharmaceutical Chemistry, R.V.S. College of Pharmaceutical Sciences, Sulur, Coimbatore Tamilnadu, IN
4 Department of Pharmacognosy, R.V.S. College of Pharmaceutical Sciences, Sulur, Coimbatore Tamilnadu, IN
1 Department of Pharmacology, R.V.S. College of Pharmaceutical Sciences, Sulur, Coimbatore-641402, Tamilnadu, IN
2 Department of Pharmacognosy, R.V.S. College of Pharmaceutical Sciences, Sulur, Coimbatore, Tamilnadu, IN
3 Department of Pharmaceutical Chemistry, R.V.S. College of Pharmaceutical Sciences, Sulur, Coimbatore Tamilnadu, IN
4 Department of Pharmacognosy, R.V.S. College of Pharmaceutical Sciences, Sulur, Coimbatore Tamilnadu, IN
Source
Research Journal of Pharmacology and Pharmacodynamics, Vol 6, No 3 (2014), Pagination: 126-128Abstract
Aim of this study was to evaluate the in vivo anti-snake venom activity of leaves of Orthosiphon stamineus were studied against Cobra (Naja Naja) venom. The in vivo study was carried out by using Swiss albino mice in modifying the lethal effect of the test dose of the Cobra venom. In in vivo model the effectiveness of the extract was evaluated by oral administration of two different doses (200 and 400 mg/kg) of the methanolic extract of the leaves of Orthosiphon stamineus 5 minutes prior to the injection of the venom and the percentage of mortality was observed. The extract markedly decreased the percentage of mortality in venom induced toxicity in mice at the dose of 400mg/kg b.w which indicates the significant anti-snake venom activity of the plant there by justifying its use in the indigenous system of medicine. The present study has confirmed the ethnomedical use of the plant for the treatment of snake bite.Keywords
Snake venom, Naja Naja, Orthosiphon stamineus, Leaves, Mice.References
- Achyuthan, K. E. and L. K. Ramachandran Cardiotoxin of the Indian cobra (Naja naja) is a pyrophosphatase. J. Biosci ; 1981; 3(2):149-156.
- B. S. Meldrum Actions of whole and fractionated Indian Cobra (Naja naja) venom on skeletal muscle Brit. J. Pharmacol.; 1965; 25; 197-205.
- Dona DD, Nguyen NH, Doan HK, et al. studies on the Individual and combined Diuretic Effects of Four Vietnamese Traditional Herbal Remedied (Zea Mays, Imperate cylindrical, plantago major and Orthosiphon stamineus). J. Ethnopharmacol. 1992; 36 (3): 225-31.
- Ecobichon DJ. The basis of toxicology testing. 2nd ed, CRC Press: New York; 1997, pp. 43-60.
- Gaitonde BB, Bhattacharya S. An epidemiological survey of snake bite cases in India. Snake. 1980;12 : 129-33.
- Galyuteva, G.I., N.A. Benson, Comparative evaluation of the diuretic activity of leaves and leaf tissue culture biomass of Orthosiphon stamineus Benth. Rastite 'Nye Resursy; 1990; 26 (4); 559-565.
- Ghosh MN. Fundamentals of Experimental Pharmacology 1984.
- Mariam, A., M.Z. Asmawi, et al. Hypoglycaemic activity of the aqueous extract of Orthosiphon stamineus. Fitoterapia 1999; 67 (5): 465-468.
- Masuda, T., Masuda, et al. Orthosiphol A and B, Novel diterpenoid inhibitors of TPA (12-O-tetradecanoylphorbol-13-acetate) - induced inflammation, from Orthosiphon stamineus. Tetrahedron; 1992 ; 48 (33) : 6787-6792.
- OJ Ode; IU Asuzu . Toxicon; 2006; 48; 331-342.