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Belonwu, D. C.
- Comparative Phytochemistry of Peddled Yoruba Medicinal Formulations
Abstract Views :526 |
PDF Views:487
Authors
Affiliations
1 Department of Biochemistry, University of Port-Harcourt, Choba, Rivers state, NG
1 Department of Biochemistry, University of Port-Harcourt, Choba, Rivers state, NG
Source
Indian Journal of Drugs and Diseases, Vol 2, No 3 (2013), Pagination: 259-269Abstract
Yoruba formulations are now widely accepted as medicinal formulations in rural and most urban areas among the low income earners. This study was aimed to evaluate the phytochemical constituents of these formulations. Five different formulations were purchased from traditional medical dispensers in Aluu, Choba, Alakahia, Rumuosi and Rumuokoro communities in Obio/Akpor Local Government Area of Rivers state Nigeria. Phytochemical studies revealed the presence of alkaloids, flavonoids, terpenoids, saponins, phenolics and cardiac glycosides. Phylobatanins was absent in all formulations while anthraquinones was absent in the formulation purchased in Aluu community. Quantitative analysis revealed the major components in all five formulations as; Tanins (8.35±0.327 -Aluu; 12.03±0.556-Choba; 5.67±0.231- Alakahia; 7.53±0.456-Rumuosi; 5.63±0.031- Rumuokoro), Flavonoids (4.24±0.21-Aluu; 9.06±0.055- Choba; 5.54±0.051- Alakahia; 7.35±0.021- Rumuosi; 8.13±0.062- Rumuokoro), then alkaloids (2.75±0.07-Aluu; 0.82±0.020- Choba; 5.41±0.100- Alakahia; 3.47±0.023- Rumuosi; 4.77±0.157- Rumuokoro). These phytochemicals have been implicated in several medicinal capacities, hence, the acclaimed medicinal properties of these Yoruba medicinal formulations.Keywords
Phytochemistry, Yoruba FormulationsReferences
- Anderson GD (2004) Phytochemicals 2004
- Ashok K, Rajkumar P and Kanimozhi M (2010) J. Sci. Res. 5(3), 157-162
- Parekh J and Chanda S (2007) Invitro antibacterial activity of the crude methanol extract
- of Woodfordia fruticosa kurz. flower (Lythraceae). Braz. J. Microbiol. 38, 204-207.
- Balasundaram A, Kumar PR, John G, and Selvakumar BN (2011) Antimicrobial activity
- of the leaf extracts of two medicinal plants against MRSA (Methicilin Resistant
- Staphylococcus aureus) from Human Urinary Tract Pathogens. Res. J. Microbiol., 6: 625-631.
- Braca A, Sortino C, Politi M, Morelli I and Mendez J (2002) Antioxidant activity of flavonoids from Licania licaniaeflora. J. Ethanol. Pharmacol. 79, 379-381
- Cushnie TPT and Lamb AJ (2005) Antimicrobial activity of flavonoids. Int. J. Antimicrobial Agents 26 (5), 343-356
- Cushnie TPT and Lamb AJ (2011) Recent advances in understanding the antibacterial properties of flavonoids. Int. J. Antimicrobial Agents 38 (2), 99-107
- David O Kennedy and Emma L Wightman (2011) Herbal extracts and phytochemicals: Plant Secondary Metabolites and the Enhancement of Human Brain Function. Brain, Performance and Nutrition Research Centre, School of Life Sciences, Northumbria University, Newcastle
- De Silva T (1997) Medicinal plants for forest conservation and health care: Industrial utilization of medicinal plants in developing countries. Global initiative for traditional systems (gifts) of health. Food Agri. Organ. United Nat. 11, 34-44.
- De Sousa RR, Queiroz KC, Souza AC, Gurgueira SA, Augusto AC, Miranda MA, Peppelenbosch MP, Ferreira CV and Aoyama H (2007) Phosphoprotein levels, MAPK activities and NFkappaB expression are affected by fisetin. J. Enzyme Inhib. Med. Chem. 22 (4), 439-444
- Gills LS (1992) Ethnomedical uses of plants in Nigeria. University of Benin press. Nigeria, 276
- Harborne IB (1973) Phytochemical methods: A guide to modern techniques of plant analysis. 2nd edn, Chapman and Hall, NY. pp: 88-185
- Hayashi T, Okamuka K, Kawasaki M and Morita N (1993) Production of titerpernoids by cultured cells from two Chemotypes Scoparia Dulcis Phytochemistry. 35(2), 353-356
- Inavova D, Gerova D, Chervenkov T and Tankova T J (2005) Ethnopharmacol. 96, 154-150.
- Joseph B and Jini D (2011) Insight into the Hypoglycaemic Effect of Traditional Indian Herbs Used in the treatment of Diabetes. Res. J. Med. Plant. 5, 352-376
- Kadiri AB (2008) Evaluation of medicinal herbal trade (Paraga) in Lagos state of Nigeria. Enthnobotanical leaflets 12, 677-681
- Katie E Ferrell and Thorington Richard W (2006) Squirrels: the animal answer guide. Baltimore: Johns Hopkins University Press. pp: 91
- Lapidot T, Harel S, Akiri B, Granit R and Kanner J (1999) pH-dependent forms of red wine anthocyanins as antioxidants. J. Agricultural and Food Chem. 47, 67-70.
- Liu RH (2004) Potential synergy of phytochemicals in cancer prevention: mechanism cells by extracts of fruits and vegetables. Food J. Nutr. 134, 34795-34855
- Mandal V, Mohan Y and Hemalatha S (2007) Pharmacog. Rev. 1, 7-18
- Manske RHF (1965) The Alkaloids Chemistry and Physiology. Volume VIII- NY: Academic Press. pp: 673
- McGEE Harold (2004) On food and cooking: the science and lore of the kitchen. New York: Scribner. pp: 714
- Trease GE and Evans WC (2002) Pharmacognosy. 15th Edn. Saunders, pp: 214-393
- Nebedum J, Ajeigbe K, Nwobodo E, Uba C, Adesanya O, Fadare O and Ofusori D (2009) Comparative study of the ethanolic extracts of four Nigerian plants against some pathogenic microorganisms. Res. J. Med. Plant. 3, 23-28
- Olowokudejo JD, Kadiri AB and Travih VA (2008) An ethnobotanical survey of herbal markets and medicinal plants in Lagos state of Nigeria. Ethnobotanical leaflets. 12, 851-865
- Okwu de (2001) Evaluation of the chemical composition of indigenous spices and flavouring Agents. Global J. Pure Appl. Sci. 7(3), 455-459
- Pamploma-Roger GD (1999) The Encyclopedia of medicinal plants. Education and health library, 2nd Edn. Spain, pp:76-97
- Pietta P (2000) Flavonoids as antioxidants. J. Natural Product. 63, 1035-1042
- Robert Alan Lewis (1998) Lewis’ dictionary of toxicology. CRC Press. pp: 51
- Rhoades David F (1979) Evolution of Plant Chemical Defense against Herbivores
- Schuier M, Sies H, Illek B and Fischer H (2005) Cocoa-related flavonoids inhibit CFTR- mediated chloride transport across T84 human colon epithelia. J. Nutr. 135 (10), 2320-2325
- Siddiqui S, Serma A, Rather A, Jabeen F and Meghvansi MF (2009) Adv. Biol. Res. 3(5-6), 188-195
- Singha SC (1965) Medicinal Plants in Nigeria. Published by the Nigerian National Press Ltd., Apapa, Lagos, Nigeria.
- Sofowora A (1993) Medicinal Plants and Traditional Medicine in Africa. 2nd Edn. Spectrum Books Limited, Ibadan, Nigeria, pp: 1-153
- Soladoye MO, Sonibare MA and Rosanwo TO (2008) J. Applied Sciences Asian Net-work for Scientific Information. 1, 1-6
- Sonibare MA, Soladoye MO and Esan O (2009) Africa J. Traditional, Complementary and Alternative Medicines (AJTCAM). 6 (4), 518-525
- Trease GE and Evans WC (1989) A textbook of Pharmacognosy (13th edition) Bacilluere Tinal Ltd, London.
- Trease GE and Evans WC (1983) Textbook of Pharmacognosy. 12th edn. Balliese Tindall and Company Publisher, London. pp. 343-383.
- United Nations Educational Scientific and Cultural Organization UNESCO (1997). Culture and health, orientation texts. World decade for cultural dev. 1988-1997. Doc. CLT/DEC/PRO, Paris, France, Pg.129.
- United Nations Educational Scientific and Cultural Organization (UNESCO) (1998). Terminal Report. Promotion of Ethnobotany and sustainable use of plant resources in Africa. Pg.60, Paris
- Effect of Selected Yoruba Medicinal Formulations on Certain Haematological Parameters of Wistar Albino Rats
Abstract Views :379 |
PDF Views:372
Authors
Affiliations
1 Department of Biochemistry, University of Port-Harcourt, Choba, Rivers state, NG
1 Department of Biochemistry, University of Port-Harcourt, Choba, Rivers state, NG
Source
Indian Journal of Drugs and Diseases, Vol 2, No 3 (2013), Pagination: 270-275Abstract
Yoruba medicinal formulations derived from plant extracts are fast becoming one of the most widely consumed medicinal formulation in the rural areas of Nigeria. The aim of this study was to screen and evaluate the effect of these medicinal formulations on cetain haematological parameters of wistar albino rats. Sixty-four rats irrespective of sex were used in this study. They were divided into six groups (control and Groups A-E); with groups A-E split into three groups for testing at week 2, 4 and 6. Each sub group contained four rats and was administered 2.9μl/Kg B.W of each medicinal formulation. Cage side examination was done daily to observe overt signs of toxicity (salivation, lacrimation, yellowing of fur etc). The formulation resulted in a significant increase then reduction in the body weight. The haematological parameters surveyed increased significantly at p < 0.05, most especially the WBC count. The increase in WBC also affirmed the presence of toxins in this formulation. The histological findings of the liver sections indicated gross cirrhosis, degeneration, inflammation and apoptosis in the experimented groups as compared to the control group. These findings suggest that, despite the reported and acclaimed benefits of this formulation, irrespective of the source, its use as a medicinal formulation should be with extreme caution. Regulation of dose and frequency of consumption of this formulation may reduce its toxic side effectsKeywords
Yoruba, Haematological ParametersReferences
- Abolaji O.A, Adebayo A.H, Odesanmi O.S (2007). Nutritional Qualities of Three Medicinal Plant Parts (Xylopia aethiopica, Blighia sapida and Parinari polyandra) commonly used by Pregnant Women in the Western Part of Nigeria. Pak. J. Nutr. 6: 665-668.
- Adebayo .A.H, Aliyu .R., Gatsing .D., Garba .I.H. (2006). The Effects of Ethanolic Leaf Extract of Commiphora africana (Burseraceae) on Lipid Profile in Rats. Int. J. Pharmacol. 2: 618-622.
- Chevellier, .A. The Encylopedia of Medical Plant. London.Dorling Kindersley Ltd. (online), 1996. Http://www.chclibrary. org/plant.html
- David L.W, Vincent M. (1985) Biochemistry in clinical practice. New York: Worth Publishers; Test indicating hepatocellular damage; p. 142.
- De Smet PAGM. Health risk of Herbal Remedies. Drug Safety 1995; 13(2): 81-93.
- Kadiri .A.B (2008). Evaluation of medicinal herbal trade (Paraga) in Lagos state of Nigeria. Enthnobotanical leaflets 12;p677-681.
- MAC, 2002, Safety of herbal medicinal products. MAC, 2002. Www.mhra.gov.uk/home/idcplg?Idcservice
- Murray R.K. (2000) Red & White Blood Cells. In: Harpers’s Biochemistry (R.K. Granner, P. A. Mayes and V.W. Rodwell, eds.) Mcgraw-Hill, USA. 2000; pp780-786.
- Nerbert .W.T. Fundamental of clinical chemistry. In: Burtis CA, Ashwood ER, editors. Tietz Texbook of Clinical Chemistry. 3rd ed. Philadelphia: W.B. Saunders; 1983. Pp. 1056–92.
- Nkosi C.Z, Opoku A.R, Terblanche S.E. (2005) Effect of pumpkin seed (Cucurbita pepo) protein isolate on the activity levels of certain plasma enzymes in ccl4 induced liver injury in low protein fed rats. Phytother Res. 2005;19:341–5.
- OLOWOKUDEJO .J.D; KADIRI .A.B; TRAVIH V.A (2008). An ethnobotanical survey of herbal markets and medicinal plants in Lagos state of Nigeria. Ethnobotanical leaflets 12;p 851-65.
- Olson .H, Betton .G, Robinson .D, Thomas .K, Monro .A, Kolaja .G, Lil Y .P, Sanders .J, Sipes .G, Bracken .W, Dorato .M, Deun .K.V, Smith .P, Berger .B, Heller .A (2000). Concordance of toxicity of pharmaceuticals in humans and in animals. Regul. Toxicol. Pharmacol. 32: 56-67.
- Shah .M, Patel .P, Phadke .M, Menon .S, Francis .M, Sane .R.T. (2002) Evaluation of the effect of aqueous extract from powder of ischolar_main, stem, leaves and whole plant of Phyllanthus debilis against ccl4 induced rat liver dysfunction. Indian Drug;39:333–7.
- Taylor J.L.S, Rabe .T., Mcgaw L.J., Jäger A.K., Van Staden .J. (2001). Towards the scientific validation of traditional medicinal plants. Plant Growth Regul. 34: 23-37. Adebayo AH, Tan NH, Akindahunsi AA, Zeng GZ, Zhang YM (2010). Anticancer and antiradical scavenging activity of Ageratum Conyzoides L. (Asteraceae). Phcog. Mag. 6: 62-66.
- Yakubu M.T, Akanji M.A, Oladiji A.T (2007). Haematological evaluation in male albino rats following chronic administration of aqueous extract of Fadogia agrestis stem. Pharmacog. Mag. 3: 34.
- Yakubu M.T, Akanji M.A, Oladiji A.T (2008). Alterations in serum lipid profile of male rats by oral administration of aqueous extract of Fadogia argrestis stem. Res. J. Med. Plant. 2: 66-73.
- Phytochemical Analysis of the Yoruba Medicinal Formulations- "Gbogbo Nise" and its Effect on Some Liver Enzymes
Abstract Views :734 |
PDF Views:1149
Authors
Affiliations
1 Department of Biochemistry, University of Port-Harcourt, Choba, Rivers state, NG
1 Department of Biochemistry, University of Port-Harcourt, Choba, Rivers state, NG
Source
Indian Journal of Drugs and Diseases, Vol 2, No 5 (2013), Pagination: 280-287Abstract
The Yoruba formulation called Gbogbo nise is one of the most widely consumed medicinal formulation in the rural areas of Nigeria. The aim of this study was to screen for the various phytochemicals in this medicinal formulation and the effects of these formulations on some liver enzymes of wistar albino rats. Sixty-four rats irrespective of sex were used in this study. They were divided into six groups (control and Groups A-E); with groups A-E split into three sub-groups for testing at week 2, 4 and 6. Each sub group contained four rats and was administered 2.9μl/Kg B.W of each medicinal formulation. Phytochemical screening indicated the presence of alkaloids, saponins, tannins, flavonoids and terpenoids. Biochemical examination of the serum of experimental groups after 2 weeks of administration, showed an initial reduction in activities of AST, ALT and ALP when compared with control groups. For the results at weeks 4 and 6, all five formulations resulted in significant increase in the level of these marker enzymes. Thus the prolong administration of these medicinal formulation at the dosage used in the study, results in rise in liver enzymes and may be indicative of hepatic damage.Keywords
Yoruba, Gbogbo Nise, Phytochemicals,liver EnzymesReferences
- Abd el Rahman HF, Skaug N and Whyatt A (2003) Volatile compounds in crude salvadora persica extracs. Pharm. Biol. 41, 392-404
- Akanji MA (1986) A comparative biochemical study of the interaction of some trypanocides with rat tissue cellular system. Ph.d thesis, University of Ife, Ile-Ife.
- Butterworth PJ and Moss DW (1966) The effect of urea on human kidney alkaline phosphatase. Biochem. J. 99, 9-10
- Chevellier A (1996) The encylopedia of medical plant. London. Dorling kindersley ltd. (online). Http://www.chclibrary.org/plant.html
- David LW and Vincent M (1985) Biochemistry in clinical practice. New york: worth publishers; test indicating hepatocellular damage. pp: 142
- Harborne IB (1973) Phytochemical methods: a guide to modern techniques of plant analysis. 2nd edn, chapman and hall, NY, pp:88-185
- Ingham JL (1973) Disease resistance in higher plants. The concept of pre-infectional and post- infectional resistance. Phytopathol. Z. 78, 314-335.
- Iwu MM (1993) In: Handbook of african medicinal plants. Crc press, ll.c. USA. pp:1-13
- Lambo JO (1979) The healing powers of herbs with special reference to obstetrics and gynaecology’ african medicinal plants (ed sofowora e a). University of ife press ife, Nigeria. pp: 23
- Nkosi CZ, Opoku AR and Terblanche SE (2005) Effect of pumpkin seed (cucurbita pepo) protein isolate on the activity levels of certain plasma enzymes in ccl4 induced liver injury in low protein fed rats. Phytother. Res.19, 341–345
- Malomo SO (2000) Toxicological implications of ceftriaxone administration in rats. Nig. J. Biochem. Mol. Biol. 15, 33-38
- Nwogu LA, Alisi CS, Ibegbulem CO and Igwe CU (2007) Phytochemical and antimicrobial activity of ethanolic extract of landolphia owariensis leaf. Afr. J. Biotechnol. 6(7),890-893
- Nwogu LA, Igwe CU and Emejulu AA (2008) Effects of landolphia owariensis on the liver function profile and haemoglobin concentration of albino rats. Afr. J. Biochem. Res. 2(12), 240-242
- Osbourn AE (1996) Preformed antimicrobial compounds and plant defense against fungal attack the plant cell, 8, 1821-1831
- Reitman S and Frankel S (1957) Colorimetric GOT and GPT determination. Am. J. Clin. Pathol. 28,56-63
- Trease GE and Evans WC (1996) Phenols and phenolic glycosides in: trease and evans pharmacognosy, 13th edn. Biliere tindall, London. pp: 832–833
- Treasure J (2000) Medical herb (online) http://www.herbological.com
- http://www.ibiblio.org 2000
- Shah M, Patel P, Phadke M, Menon S, Francis M and Sane RT (2002) evaluation of the effect of aqueous extract from powder of ischolar_main, stem, leaves and whole plant of Phyllanthus debilis against CCl4 induced rat liver dysfunction. Indian drug. 39, 333-337
- Shahjahan M, Sabitha KE, Mallika J and Shyamala-Devi CS (2004) Effect of Solanum trilobatum against carbon tetrachloride induced hepatic damage in albino rats. Indian J. Med. Res. 120,194-198
- Sofowora EA (1993) In: Medicinal plants and traditional medicine in Africa. (2nd ed), spectrum books limited. pp: 26-30
- Wright PJ and Plummer DT (1974) The use of urinary enzyme measurement to detect renal damages caused by nephrotoxic compounds. Biochem. Pharmacol. 12, 65
- Yakubu MT, Bilbis MT, Lawal M and Akanji MA (2003) Effect of repeated administration of sildenafil citrate on selected enzyme activities of liver and kidney of male albino rats. Nig. J. Pure & Appl. Sci. 18, 1395-1400
- Effect of Selected Yoruba Medicinal Formulations on Certain Biochemical Parameters in Wistar Albino Rats
Abstract Views :529 |
PDF Views:389
Authors
Affiliations
1 Department of Biochemistry, University of Port-Harcourt, Choba, Rivers state, NG
1 Department of Biochemistry, University of Port-Harcourt, Choba, Rivers state, NG
Source
Indian Journal of Drugs and Diseases, Vol 2, No 5 (2013), Pagination: 288-293Abstract
Yoruba medicinal formulations derived from plant extracts are fast becoming one of the most widely consumed medicinal formulation in the rural areas of Nigeria. The aim of this study was to screen evaluate the effect of this medicinal formulation on cetain biochemical parameters of wistar albino rats. Sixty-four rats irrespective of sex were used in this study. They were divided into six groups (control and Groups A-E); with groups A-E split into three groups for testing at week 2, 4 and 6. Each sub group contained four rats and was administered 2.9μl/Kg B.W of each medicinal formulation. Cage side examination was done daily to observe overt signs of toxicity (salivation, lacrimation, yellowing of fur etc). The formulation resulted in a significant increase then reduction in the body weight. Markers of hepatocyte injury; alanine transaminase and aspartate transaminase, were initially reduced but increased at week 4. Same was observed for the cholestasis marker alkaline phosphatase. The levels of serum creatinine, urea and blood urea nitrogen steadily reduced over time. The histological findings of the liver sections indicated gross cirrhosis, degeneration, inflammation and apoptosis in the experimented groups as compared to the control group.Keywords
Yoruba, Biochemical ParametersReferences
- Abolaji OA, Adebayo AH, Odesanmi OS (2007) Nutritional Qualities of Three
- Medicinal Plant Parts (Xylopia aethiopica, Blighia sapida and Parinari polyandra)
- commonly used by Pregnant Women in the Western Part of Nigeria. Pak. J. Nutr. 6,665-668
- Adebayo AH, Aliyu R., Gatsing D and Garba IH (2006) The Effects of Ethanolic Leaf
- Extract of Commiphora africana (Burseraceae) on Lipid Profile in Rats. Int. J.Pharmacol. 2, 618-622.
- Chevellier A (1996) The Encylopedia of Medical Plant. London.Dorling Kindersley Ltd. (online), Http://www.chclibrary.org/plant.html
- David LW and Vincent M (1985) Biochemistry in clinical practice. New York: Worth Publishers; Test indicating hepatocellular damage. pp: 142
- De Smet PAGM (1995) Health risk of Herbal Remedies. Drug Safety.13(2), 81-93
- Kadiri AB (2008) Evaluation of medicinal herbal trade (Paraga) in Lagos state of Nigeria. Enthnobotanical leaflets 12, 677-681
- Mac (2002) Safety of herbal medicinal products. www.mhra.gov.uk/home/idcplg?Idcservice
- Murray RK (2000) Red & White Blood Cells. In: Harpers’s Biochemistry (Granner RK, Mayes PA and Rodwell VW, eds.) Mcgraw-Hill, USA. pp:780-786
- Nerbert WT (1983) Fundamental of clinical chemistry. In: Burtis CA, Ashwood ER, editors. Tietz Texbook of Clinical Chemistry. 3rd ed. Philadelphia: Saunders WB: pp: 1056–1092
- Nkosi CZ, Opoku AR and Terblanche SE (2005) Effect of pumpkin seed (Cucurbita pepo) protein isolate on the activity levels of certain plasma enzymes in ccl4 induced liver injury in low protein fed rats. Phytother. Res.19,341–345
- Olowokudejo JD, Kadiri AB, Travih VA (2008) An ethnobotanical survey of herbal markets and medicinal plants in Lagos state of Nigeria. Ethnobotanical leaflets 12,851-865
- Olson H, Betton G, Robinson D, Thomas K, Monro A, Kolaja G, Lil YP, Sanders J, Sipes G, Bracken W, Dorato M, Deun KV, Smith P, Berger B, Heller A (2000) Concordance of toxicity of pharmaceuticals in humans and in animals. Regul. Toxicol. Pharmacol. 32, 56-67
- Shah M, Patel P, Phadke M, Menon S, Francis M and Sane RT (2002) Evaluation of the effect of aqueous extract from powder of ischolar_main, stem, leaves and whole plant of Phyllanthus debilis against CCl4 induced rat liver dysfunction. Indian Drug. 39,333-337
- Taylor JLS, Rabe T, Mcgaw LJ, Jäger AK and Van Staden J (2001) Towards thescientific validation of traditional medicinal plants. Plant Growth Regul. 34, 23-37
- Adebayo AH, Tan NH, Akindahunsi AA, Zeng GZ, Zhang YM (2010) Anticancer and antiradical scavenging activity of Ageratum Conyzoides L. (Asteraceae). Pharmacog. Mag. 6, 62-66
- Yakubu MT, Akanji MA and Oladiji AT (2007) Haematological evaluation in male albino rats following chronic administration of aqueous extract of Fadogia agrestis stem. Pharmacog. Mag. 3,34
- Yakubu MT, Akanji MA and Oladiji AT (2008) Alterations in serum lipid profile of male rats by oral administration of aqueous extract of Fadogia argrestis stem. Res. J. Med. Plant. 2, 66-73
- Invivo Effect of Microgynon and Primolut-n on Plasma Sodium and Potassium of Wistar Albino Rat
Abstract Views :594 |
PDF Views:335
Authors
Affiliations
1 Department of Biochemistry, University of Port Harcourt, Nigeria. P.M.B 5323, Port Harcourt, NG
1 Department of Biochemistry, University of Port Harcourt, Nigeria. P.M.B 5323, Port Harcourt, NG
Source
Indian Journal of Drugs and Diseases, Vol 1, No 4 (2012), Pagination: 92-96Abstract
Microgynon (0.15mg levonorgestrel and 0.03mg ethinylestradiol), is an oral contraceptives Primolut -N a mini pill (5mg norethisterone) were analysed for their in-vivo effects on albino rat plasma sodium and potassium levels. Studies showed that the drugs decreased sodium levels with microgynon showing the highest decrease of 29.85% at highest concentration level of 3.6μg /100g (94.00 ± 28.50mmol/l) (P < 0.05), followed by Primulot-N (102 ± 28.50 mmol/l). Investigations also revealed that the drugs decreased plasma potassium levels. Microgynon had the highest decrease of 88.88% for the highest dose of 3.60μg/100g body wt, while the lowest decrease of 22.22% was observed for the lowest dose of 0.36μg/100g).The sodium element plays an important role in salt and water balance in the body. The metabolism of sodium and potassium is closely linked with the maintenance of fluid balance and with the regulation of acid-base status, Elevated levels are related to acidosis as well as too much water crossing the cell membrane. The potassium element is found primarily inside the cells of the body. The random use of the drugs in our society today especially as most women abuse these drugs demands for more biochemical research to elucidate the effects of these drugs not only on the hormones but also on other biochemical parameters like the body electrolytes. This result indicates that laboratory tests are needed for women before using these drugs.Keywords
Microgynon, Primulot-n, Plasma Sodium and PotassiumReferences
- Bracken MB and Hellenbrand KG and Holford TR (1990) Conception delay after oral contraceptive use: The effect of estrogen dose. Fertil. Steril. 53,21.
- CHPE, Division of Reproductive Health (1984) Family Planning Methods and Practice: Africa. U. S. Public Health service. Department of Health and Human Services, Atlanta Georgia 30333. USA.
- Ghoneim SM, Toppozada RK, El-Heneidy AR and Taha MM (1975) The effects of an oral contraceptive on acid-base balance, blood gases and electrolytes. J. Contraception.12(4),395 -405.
- Grimes DA, Mishell DR, Jr. and Speroff L (1993) Contraceptive choices for women with medical problems. Am. J. Obstet. Gynecol. 198,625-630.
- Henderson M, Dorflinger J, Fishman J, Foster HW, Gump FE, Hellman S, Hulka BS, Mattison DR, McKay SAR, Moses LE, Norsigian J, Potts M, Schwartz NB, Smith H, Stolley PD and Wiggins PV (1991) Oral contraceptives and breast cancer. National academy press. pp: 1-77.
- Henry RJ (1974) Clinical Chemistry, Principles and Technics, 2nd Edn, Harper and Row. pp: 525.
- Kay CR, Crombie DL, Kuenssberg EV, Pinsent RJFH, Richards B, Smith A and Crowther CH (1974) Oral contraceptives and health. The royal college of general practitioners study. Am. J. Obstet. Gynecol. 10,150.
- Kuhl H and Goethe JW (1990) Pharmacokinetics of oral contraceptives, steroids and drug interaction. Am. J. Obst. Gynaecol. 163, 2113.
- Mishell DR Jr (1982) Nonecontraceptive health benefits of oral steroidal contraceptives. Am. J. Obstet. Gynecol. 142, 809.
- Scott JA and Brenner PF (1978) Comparison of the effects of contraceptive steroid formulations containing two doses of estrogen on pituairtary function. Fertil. steril. 30,141.
- Skouby SO and Jesperson J (1990) Oral contraceptives in the nineties, metabolic aspects, facts and fiction. Am. J. Obstet Gynecol. 163,276.
- Smith RP and Sizto R (1983) Metabolic effects of two triphasic formulations containing ethinyl estradiol and dl-norgestrel. J. Contraception. 28 (2),189 -199.
- Terri AE and Sesin PG (1958) Fundamentals of Clinical Chemistry. Am. J. Clin. Path. 29,86.
- Tietz NW (1995) Clinical guide to laboratory tests, 3rd edn. WB Saunders Co. Philadelphia, PA. 874.
- Trinder P (1951) Invitro determination of sodium in serum. Analyst. 76,596.
- Wootton IDP and Freeman H (1982) Microanalysis in medical biochemistry, 6th Edn, Churchill Livingstone Inc. NY, USA. pp: 1-190.
- World Health Organization Task Force on Oral Contraceptives (1982). A randomized, double-blind study of two combined and two progestogen-only oral contraceptives. Contraception. 25,243.
- A Study of the invivo Effect of Microgynon and Primolut-n on Albino Rat Plasma Aspartate Amino Transferase (EC 2.6.1.1) and Alanine Amino Transferase (EC 2.6.1.2) at 37°c, Ph = 9.8
Abstract Views :416 |
PDF Views:313
Authors
Affiliations
1 Department of Biochemistry, University of Port Harcourt, Nigeria. P.M.B 5323, Port Harcourt, NG
1 Department of Biochemistry, University of Port Harcourt, Nigeria. P.M.B 5323, Port Harcourt, NG
Source
Indian Journal of Drugs and Diseases, Vol 1, No 4 (2012), Pagination: 97-102Abstract
Oral contraceptives namely Microgynon a combined pill (0.15mg levonorgestrel and 0.03mg ethinylestradiol) and Primolut -N a mini pill (5mg norethisterone) were analysed for their in-vivo effects on albino rat plasma and erythrocyte aspartate amino transferase (AST). The in-vivo effects of the oral contraceptives on albino rat plasma and erythrocyte AST showed that the drugs inhibited the activity of the enzymes in a concentration dependent manner. The effect of the drugs on the enzymes were also time dependent with the highest inhibition obtained at 24 hours duration while the least inhibition occurred at 2 hours duration Microgynon showed the highest inhibition (7.00 ± 0.00 vs. control 31.00 ± 0.00 U/L) (P < 0.05) followed by Primolut (16.00 ± 0.00 vs. control 27.00 ± 4.00 U/L). The erythrocyte AST activity was also inhibited. The highest inhibition values obtained were Microgynon (36.00 ± 0.00 U/L) then Primolut (41.00 ± 0.00 U/L). The least inhibition values obtained were Microgynon and Primolut (67.00 ± 0.00). The in-vivo effects of the oral contraceptives on rat plasma and erythrocyte ALT showed that the drugs activated the activity of the enzymes in a concentration dependent manner. The effect of the drugs on the enzymes were also time dependent with the highest activation obtained at 24 hours duration while the least activation occurred at 2 hours duration. Primolut showed the highest activation (18.00 ± 0.00 U/L). The erythrocyte enzymes showed higher activity than the plasma enzymes. Microgynon showed the highest activity (50.00 ± 2.00 U/L). This result indicates that liver function tests are needed for women before using these drugs.Keywords
Microgynon, Primolut –NReferences
- Brenner PF, Mishell DR Jr and Stanezyk FZ (1977) Serum levels of D-norgestrel, luteinizing hormone, follicle stimulating hormone, estradiol, and progesterone in women during and following ingestin of combination oral contraceptive containing dl-norgestrel. Am. J. Obstet. Gynecol. 129,133.
- Briggs M (1980) Effects of oral contraceptive agents on vitamin and mineral requirements. J. Am. Diet Assoc. 5, 160.
- CHPE, Division of Reproductive Health (1984) Family planning methods and practice. US public health service. Department of Health and Human Services, Atlanta, Georgia 30333. USA.
- Devlin MT (1992) A textbook of Biochemistry with clinical correlation 3rd ed. John Wiley and sons publication USA.pp: 100.
- Grimes DA, Mishell DR Jr and Speroff L (1993) Contraceptive choices for women with medical problems. Am. J. Obstet. Gynecol. 198, 625-630.
- Hargreaves T (1969) Oral contraceptives and liver function. J. Clin. Pathol. Suppl. 3, 1-10.
- Kaunitz AM (2004) Enhancing oral contraceptive success: the potential of new formulations. Am. J. Obstet. Gynecol. 190 (4), 23-29.
- Kay CR, Crombie DL, Kuenssberg EV, Pinsent RJFH, Richards B, Smith A, Crowther CH (1974) Oral contraceptives and health. The royal college of general practitioners study. Am. J. Obstet. Gynecol. 10,150.
- Kuhl H and Goethe JW (1990) Pharmacokinetics of oral contraceptives, steroids and drug interaction. Am. J. Obstetric & Gynaecol. 163, 2113.
- Mishell DR Jr, Stanezyk FZ and Hiroi M (1976) Steroid contraception. In: Crosignami PC, Mishell DR Jr (eds): Ovulation in the Human. London, Academic press. pp: 10.
- Ohno H, Tojo H, Kajimura T and Nomura M (1994) Increased serum alkaline phosphatase induced by DT-5061, an oral contraceptive, in rats. J. Toxicol. Sci. 19 (3), 507-518.
- Reitman S and Frankel S (1957) In vitro determination of Glutamic-Oxaloacetic Transaminase (GOT) and Glutamic-Pyruvic transaminase (GPT) in serum. Am. J. Clin. Path. 28,56.
- Skouby SO and Jesperson J (1990) Oral contraceptives in the nineties, metabolic aspects, facts and fiction. Am. J. Obstet Gynecol. 163, 276.
- Swyer GIM (1982) Petency of pregestogens in oral contraceptives-further delay of menses data. Contraception. 26,23.
- Sy FS, Osteria TS, Opiniano V and Gler S (1986) Effects of oral contraceptives on liver function tests of women with schistosomiasis in the Philippines. J. Contraception. 34(3), 283 -294.