April - 2013 (Volume-3 ~ Issue-4 ~ Part-2)

Paper Type

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Research Paper

Title

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Use of Aphrodisiacs amongst women in Kano, northern Nigeria

Country

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Nigeria

Authors

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D Garba || I S Abubakar || I A Yakasai || M K Magashi

Page No.

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1-04

Paper Index

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DOI : 10.9790/3013-0342014  

ANED :: DOI :05.3013/03420104

An aphrodisiac is a substance that increases sexual desire. Many foods, drinks, and behaviors have had a reputation for making sex more attainable and/or pleasurable. Men and women alike have continued to use aphrodisiacs whether or not these drugs have any scientific basis of truly improving sexual satisfaction without regards to their composition. Objective: To look at the use of medications to enhance sexual performance among women attending gynaecology clinic in Aminu Kano Teaching Hospital, Kano Nigeria. Results: 500 clients were interviewed, 220 use some medications to enhance their sexual performance (44.0%). The mean age of the respondents was 27 years, SD 5.37, mean parity was 2.6 with a SD 2.43.There is a statistically significant relationship between age andparity (P=0.05). Women in monogamous relationship were found to use medication to enhance sexual satisfactioncompared to those in polygamous relationship. The herbalist/traditional houses were the major source of these medications (40.96%) followed by peer influence (30.91%), while health workers contribute only 2.27%.30% of the users felt more vaginal wetness with the use of the medications, however 37% of users felt no change in sexual activity. The medications did not meet the expectations of 49% of the users. Conclusion: The major sources of such medications are the traditionalists who never disclose the constituents of such medications.
Keywords: Aphrodisiacs, sexual performance,women

[1]. Wallen K, Zehr JL. Hormones and History. The evolution and Development of Primate Female Sexuality. J Sex Res. 2004; 41 (1) : 101-112
[2]. Kamhi E. Natural Aphrodisiacs at www.naturalnurse.com
[3]. McCall K, Meston C. Cues Resulting in Desire for Sexual Activity in Women. J sex Med. 2006; 3 (5) : 838-852
[4]. Epimedium: Wikipedia-the free encyclopedia. Accessed on 28th of November 2012
[5]. Moinier BM, Drueke TB. Aphrodite, Sex and Salt-From butterfly to man. Neph Diag Trans. 2008; 23 (2) : 2154-2161
[6]. Bellis MA, Hughes K, Calafet A, Juan M, Ramon A, et al. Sexual uses of alcohol and drugs and the associated health risks : A cross sectional study of young people in nine European cities. BMC Public Health. 2008; 8 : 115
[7]. Adinma JIB. Sexuality in Nigerian Pregnant Women: Perceptions and Practice. Aust NZ J Obstet Gynaecol. 1995; 35:3: 290
[8]. Brody S. High –Dose Acsorbic Acid Increases Intercourse frequency and improves mood: A randomized controlled clinical trial. Biol Psychiatry. 2002; 52: 371-374.
[9]. Uthman O. Geographical variations and contextual effects on age of initiation of sexual intercourse among women in aNigeria: A multilevel and spatial analysis. Int J Health Geo.2008;7:27.
[10]. Solivetti LM. Family, Marriage and Divorce in a Hausa community: a sociological model. Africa (Loud). 1994; 64 (2):252-271.
[11]. Kamatenesi-Mugisha M, Oryem-Origa H. Traditional herbal remedies used in the management of sexual impotence in western Uganda. Afr Health sci. 200; 5(1): 40-49.

 

Paper Type

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Research Paper

Title

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The Effects of Inhibitors and anti-GTF-Ib antibodyon Growth of Mutans Streptococci Streptococcus sobrinus (serotype G) N10 Strain

Country

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Iraq

Authors

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Essam F. A. Al-Jumaily || Nada H. A. Al-Mudallal || Nidhal A.A. Muhimen || Abd Al-wahid Al-Shaibany

Page No.

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05-09

Paper Index

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DOI : 10.9790/3013-0342059  

ANED :: DOI :05.3013/03420509

In this study the effect of different concentrations of inhibitors (sodium fluoride, chlorohexidine, EDTA and ZAK mouthrins) was tested on the growth of Streptococcus sobrinusserotype G N10 strain by using broth dilution method ( in liquid media) and diffusion method on solid media. It was found that different concentrations of anti- GTF-Ibantibody and EDTA were incapable to inhibit the growth of bacterial isolate whereas the inhibitors (sodium chloride and chlorohexidine ) at concentrations (18 mM) and (20mM) respectively were capable to produce a complete bacterial inhibition, and ZAK mouthrins at concentration (12mM) was able also to inhibit the bacterial growth by using broth dilution method. Also the effect of the same concentrations of these compounds within which anti – GTF-Ib antibody were tested on the enzymatic activity of purified GTF-Ib enzyme which was isolated from the same bacterial isolate. It was found that different concentrations of these compounds and the anti- GTF-Ibantibody were able to inhibit the enzymatic activity of the purified GTF-Ib with an exception of EDTA.
Keywords: Streptococcus sobrinus, chemical inhibitors(sodium fluoride, cholohexidine, EDTA and ZAK mouthrins)against GTFs, anti GTF-Ibantibody

[1]. Whiley, R. A.; Beighton, D.; Winstanley, T. G.; Fraser, H. Y. and Hardic, J. M. (1992). Streptococcus intermedius, Streptococcus constellatusand Streptococcus anginosus (the Streptococcus milleri group): associated with different body sites and clinical infections. J. Clin. Microbiol. 30: 243-244
[2]. Ajdic, D.; Mc Shan, W. M.; McLaughlin, R. E.; Savic, G.; Charg, J. and Carson, M.B. (2002). Genome sequence of Streptococcus mutans UA159, a carcinogenic dental pathogen. Proc. Natl. Acad. Sci. USA. 99: 14434-14439.
[3]. Jespersagaard, C.; Hajishengallis, G.; Hung, Y. and Michalek, S. (2000). Protective immunity against Streptococcus mutans infection in mice after intranasal immunization with glucan-binding region of Streptococcus mutans.Infe. Immun. 67(12):6543-9.
[4]. Kashket S, Paolino VJ, Lewis DA, van Houte J. In-vitro inhibition of glucosyltransferase from the dental plaque bacterium Streptococcus mutans by common beverages and food extracts. Arch Oral Biol 1985;30:821-6.
[5]. Al-Mudallal N. H. A (2006). Characterization of Glucosyltransferase of Mutans Streptococci Streptococcus sobrinus (Serotype G) (Functional and Immunological Assessment).Ph.D thesis, Biotechnology Department, College of Science, Al-Nahrain University.
[6]. Al-Jumaily, E.F., Nada H.A.Al-Mudallal, N.A.A.Muhimen, and Abd Al-Wahid Al-Shaibany (2009). Eavluation of matans streptococci local strains for production of glucosyltransferase enzyme.The 2nd Kurdistan Conference on Biological Sciences. J. Duhok Univ. Vol.12 No.1 (Special Issue)Pp. 227-232.
[7]. Al-Mudallal N. H. A. ;. Al-Jumail E. F. A ;.Al.- Muhimen N. A. and Abd Al-wahid Al-Shaibany (2011). Isolation and Purification of Glucosyltransferase from mutans streptococci Streptococcus sobrinus serotype G local isolate. Iraqi Journal of Medical Science.7:5-10.
[8]. Wunder, D. E. and Bowen, W. H. (2000). Effects of antibodies to glucosyltransferase on soluble and insolubilized enzymes.Oral Diseases. 6: 289-296.

 

Paper Type

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Research Paper

Title

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Formulation and Evaluation of Mucoadhesive Microcapsules Of Rifampicin

Country

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India

Authors

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Gottapu Prashanti

Page No.

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10-14

Paper Index

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DOI : 10.9790/3013-034201014  

ANED :: DOI : 05.3013/0342010014

Mucoadhesive microcapsules of rifampicin were prepared by orifice ionic gelation technique for a novel controlled release product. Sodium alginate, sodium carboxy methyl cellulose and chitosan were used as coating polymers in different ratios to obtain elegant microcapsules. The formulations were characterized for encapsulation efficiency, SEM analysis and invitro release studies. The microcapsules were discrete, large almost spherical and free flowing with encapsulation efficiency in the range 75 to 88% and size ranging from 780 to 882nm. Rifampicin release from these microcapsules was slow and extended over longer periods of time depending on polymer coat. Drug release was diffusion controlled and followed first order kinetics. The formulation F11 with coating ratio1:2:2 of sodium alginate and chitosan was found to be suitable for oral controlled release.

Key Words: Rifampicin, tuberculosis, sodium alginate, sodium carboxy methyl cellulose, chitosan.

[1]. Ain, Q.U; Sharma, S; Khuller, G.K; Garg, S.K,Alginate-based oral drug delivery system for tuberculosis: pharmacokinetic and therapeutic effects, J Antimicrob Chemother ,2003, 51, 931–938.
[2]. Shaik R., Singh T.R.R., Garland M.J., A David Woolfson, and Ryan F.Donnely, mucoadhesive drug delivery system J.Phaem Bioadhesion Sciences 2011 Jan-Mar;3(1):89-100
[3]. Edsman K., Hagerstrom H., Pharmacetical Applications of mucoadhesion for the oral routes.J.Pharm pharmocol.2005 Jan;57(1):3-22
[4]. Jiang L., Gao L., Wang X.,Tang L.,The applications of mucoadhesive polymers in drug delivery. Drug delivery in pharmacy.2010 Mar; 36(3):323-36
[5]. Labana, S; Pandey, R, Sharma, S; Khuller, G.K,Chemotherapeutic activity against murine tuberculosis of once weekly administered drugs (INH and RIF)encapsulated in liposomes, Int J Antimicrob Agents,.2002, 20, 301–304.
[6]. Quenelle, D. C; Winchester, G. A; Staas, J. K.Treatment of tuberculosis using a combination of sustained-release rifampin-loaded microspheres and oral dosing with isoniazid,. Antimicrobial Agents and Chemotherapy, 2001, 45, 1637–44.
[7]. Tonnesen, H. H; Karlsen, J. Alginate in drug delivery systems. Drug Development and Industrial Pharmacy, 2002, 28, 621–30.
[8]. Hejazi, R; Amiji, M. Chitosan-based gastrointestinal delivery systems. Journal of Controlled Release, 2003, 89, 151–65.
[9]. Manekar N.C. and Joshi, S.B., "Microencapsulation Technique". The Eastern Pharmacist, 1998; 47-49.
[10]. Chowdary K.P.R. and Suresh Babu K.V.V., "Studies on Micro encapsulation by Calcium Alginate". The Eastern Pharmacist, 1989; 2 : 125-126.
[11]. Pilley V. and C. M. Dangor, "Ionotropic Gelation : encapsulation of indomethacin in calcium alginate gel discs." J. of microencapsulation: 1998; 15(2):215-26.

 

Paper Type

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Research Paper

Title

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Evaluation of the Efficacy of Azadirachta Indica (Neem) Extract Gel as a Local Drug Delivery in the Treatment of Patients with Chronic Periodontitis. " A Double Blind Randomised Clinical Trial

Country

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India

Authors

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Dr. Verdine Virginia Antony ||, Dr. Deepak Prasad || , Dr. Rahamath ulla khan

Page No.

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15-21

Paper Index

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DOI : 10.9790/3013-034201521  

ANED :: DOI : 05.3013/0342015021

Periodontal diseases comprise of a group of inflammatory conditions of the supporting tissues of the teeth that are initiated by microorganism. The removal or inhibition of subgingival plaque and maintenance is dependent on continued plaque control for which adjunctive local antimicrobial therapy has shown promising results. In the present study, we explored the efficacy of Azadirachta indica (Neem) extract gel as a local drug delivery in the treatment of patients with chronic periodontitis and evaluated the clinical as well as the microbiological benefits when used as an adjunct to scaling and root planning. Method: 20 patients with chronic periodontitis in the age group of 30-55 years, with pocket depth of > 5mm with radiographic evidence of bone loss participated in the study. Following scaling and root planing the neem extract gel and placebo gel were placed at the experimental and control sites respectively. The clinical parameters were recorded at baseline, 1 month, 3 months and 6 months while the microbiological parameters were recorded at baseline, 7 days, 15 days and 30 days respectively. Results: The results showed improvements in the clinical parameters both at the control and the experimental sites. However, the experimental sites showed better results compared to the control site. The microbiological analysis proved a relative reduction of the periodontal pathogens at both the experimental as well as the control site with the control site showing a significantly higher reduction. Conclusion: Neem extract gel produced more improvements in clinical as well as microbiological parameters than the control. The approach of local delivery of a natural extract with no known side effects has proved promising results.
Keywords: Azadirachta indica (Neem), Clinical parameters, microbiological parameters, Therapeutic use.

[1]. Chirugien Dentiste Le, Traite des ou. Dents. 2vols. Paris, Mariette J. 1728. Reprinted in facsimile, Paris, Prelat, 1961. (An English translation by Lilian Lindsay appeared in 1946, published by Buttersworth and Company, London).
[2]. Cobb CM. Non surgical pocket therapy: Pharmacotherapeutics. Ann Periodontol 1996; 1: 491-566.
[3]. Carranza FA, Newman MG. Clinical periodontology. 9th ed. 2003; Harcourt (Pvt.) Ltd., India.
[4]. Rams TE and Slots J. Local delivery of antimicrobial agents in the periodontal pocket. Periodontol 2000. 1996; 10:139-159.
[5]. Journal of Ethno Pharmacology. 2004; 90: 99-103.
[6]. Zee KY et al. Bacterial morphotypes of three day old plaque in Chinese.
[7]. J Clin Periodontol 1996; 23: 403-406.
[8]. Genco. Antibiotics in the treatment of periodontal disease. J Periodontol 1981; 52: 545-558.
[9]. Moore WEC. Microbiology of periodontal disease. J Periodontol Res 1987; 22: 335-341.
[10]. Sanz et al. Differences in composition of subgingival microbiota of two periodontitis populations of different geographical origin – A comparison between Spain and Netherlands. Eur J Oral Sci 2000; 108: 383-392.

 

Paper Type

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Research Paper

Title

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Traditional Knowledge of Konda Dora Tribes, Visakhapatnam District, Andhra Pradesh, India

Country

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India

Authors

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S. B. Padal || J. Butchi Raju ||P. Chandrasekhar

Page No.

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22-28

Paper Index

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DOI : 10.9790/3013-034202228  

ANED :: DOI :05.3013/0342022028

Visakhapatnam district of Andhra Pradesh is known for Konda Dora tribe. Konda Dora tribe is divided into a number of clans such as Korra, Killo, Swabi, Ontalu, Kimud, Pangi, Paralek, Mandelek, Bidaka, Somelunger, Surrek, Goolorigune olijukula etc., Konda Dora are very dominant in the district. Frequent field trips were conducted in Konda Dora rich areas to collect the Traditional Botanical Knowledge and Ethno-medicinal plants used by the Konda Dora. Because of modernization, all the ethno-botanical knowledge is declining day by day, so there is an urgent need to document the knowledge of ethnic people. Here 68 plant species belong to 63 genus of ethno- medicinal value were recorded from Visakhapatnam district of Andhra Pradesh, India
Keywords: Traditional knowledge, ethnobotany, konda dora tribe, visakhapatnam, Andhra pradesh.

[1]. Anonymous, Ethno biology in India: A Status Report. Ministry of Environment & Forests, Govt. of India, New Delhi, 1990, 1 – 68 pp.
[2]. Hemadri, K. Rheumatism: tribal medicine. Anc. Sci. Life 1981, 1: 117-120.
[3]. Hemadri, K. & S.S. Rao. Leucorrhoea and menorrhagia: Tribal medicine. Anc. Sci. Life. 1983, 3: 40-41.
[4]. Hemadri, K & S.S. Rao . Jaundice: Tribal medicine. Anc. Sci. Life, 1984, 4: 209-212.
[5]. Ramarao, N. The Ethnobotany of Eastern Ghats in Andhra Pradesh, India. Ph.D. thesis. 1988, Bharathiar University, Coimbatore.
[6]. Jain, S.K.. Dictionary of Indian Folk Medicine and Ethnobotany. Deep Publications, 1991, New Delhi.
[7]. Basi Reddy, M., K. Raja Reddy and M. N. Reddy. Ethnobotany of Cuddapah district, Andhra Pradesh, India. Int. Journ. Pharmacogn., 1991, 29: 1-8.
[8]. Billore, K. V., T. G. Joseph and S. K. Dave, Interesting folk remedies by the Local vaidyas of Rajasthan for Swas Roga. Ethnobotany, 1998, 10: 42-45.
[9]. Chandra, K. and H. C. Pandey. Collection of plants around Agora Dodltal in Uttarakashi district of Uttar Pradesh with medicinal values and folk-lore claims. Int. J. Crude Drug Res., 1983, 21: 21-28.
[10]. Das, P. K. and R. Kanth. Ethnobotanical studies of the tribal belt of Koraput (Orissa). Bull. Medico Ethn. Bot. Res., 1998, 9(3-4): 123-128.
[11]. Girach, R. D. and Aminuddin. Ethnomedicinal uses of plants among the tribals of Singbhum District, Bihar, India. Ethnobotany, 1995, 7: 103 - 107.
[12]. Hema, L & N. Yesodamma. Importance of Medicinal Plants of Ardhagiri hill, Chittoor district, Andhra Pradesh. International Seminar on Medicinal Plants and Herbal products. 2008, 7th-9th March. Page. 45.
[13]. Jain, S. K. Studies on Indian Ethnobotany - Less known uses of 50 common plants from tribal areas of Madhya Pradesh. Bull. Bot. Surv. India, 1963, 5(3-4): 223-226.
[14]. Katewa, S. S., Ambika Nag and Buddhadev Guria. Ethnobotanical studies on wild plants for food from the Aravalli hills of South - east Rajasthan. J. Eeon. Tax Bot., 1999, 23: 259-264.
[15]. Kumar, A. K. and K. Niteswar. An enquiry into the folk lore medicines of Addateegala an agency tract of East Godavari District of Andhra Pradesh. Indian Medicine, 1983, 2: 2-4.

 

Paper Type

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Research Paper

Title

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Drug Designing An Ayurvedic Perspective

Country

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India

Authors

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Abhilash Mullasseril

Page No.

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29-33

Paper Index

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DOI : 10.9790/3013-034202933  

ANED :: DOI :05.3013/0342029033

The Computer Assisted Drug Designing and Discovery is an emerging area of Scientific research with great importance. The knowledge abstraction for achieving the goals of this research is not only limited to modern computational chemistry or pharmacy. The computational scientists are ready to widen their knowledge based on all branches of medicines and we can also find relevant and significant information from alternative medicines like ayurveda. This paper aims to correlate the modern drug discovery concept to the traditional Indian system of medicine known as Ayurveda. The computer assisted drug designing is the modern concept in which the concept of Artificial Intelligence is widely applied throughout the processes. The research for improvising methodologies adopted many terminologies from the different branches of knowledge and made the field more interdisciplinary in nature. The philosophical bases of the Ayurvedic concept of Aushadha and Tridosha theory of diagnosis are also found relevant in the field of modern drug discovery and development and are able to give new insights to the scientists and medicinal chemists.
Keywords: Drug, Drug discovery and Development, Lipinski rules, Aushadha, Pathya, Medicinal Chemistry, Ayurveda, Alternative medicines.

[1] Mitscher, A. Lester, Drug Design and Discovery: an overview in Textbook of Drug Design and Discovery (Taylor & Francis, London and New York, 2004).
[2] V.Chaitanya, R.Sangal, Natural Language Processing A Paninian Perspective, (New Delhi:PHI, 1999).
[3] G.L. Patrick, An Introduction to Medicinal Chemistry (Oxford:Oxford University Press, 2009).
[4] R.Guenin, C.H.Schneider, Penicillin derivatives are true monovalent elicitors of anaphylactic reactions. Immunology. 52, 1984, 189-96.
[5] IUPAC web site http://www.iupac.org H Van de Waterbeemed (1997) Glossary of terms used in computational drug design. Pure & Appl. Chem. 69(5), 1137-1152.
[6] Carakasamhita : Read vedic literature in Sankrit Maharshi University
[7] C.A.Lipinski, F.Lombardo, B.W.Dominy and P.J.Freeney, Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug. Deliv. Rev., 23, 1997, 3-25.
[8] Rama Vaidya Observational therapeutics: Scope, challenges, and organization. Journal of Ayurveda & Integrative Medicine, 2(4), 2011.

 

Paper Type

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Research Paper

Title

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Triterpene Glycosides from the Aerial Parts and Seeds of Bupleurum Falcatum

Country

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U.S.A

Authors

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Venkata Sai Prakash Chaturvedula || Indra Prakash

Page No.

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34-37

Paper Index

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DOI : 10.9790/3013-034203437  

ANED :: DOI :05.3013/0342034037

Phytochemical studies of the aqueous alcoholic extract of the aerial parts and seeds of Bupleurum falcatum furnished two known oleanane triterpene glycosides namely saikosaponin A, and saikosaponin D. The structures of the two isolated compounds 1-2 were characterized and their complete 1H and 13C NMR spectral assignments were made based on COSY, HMQC, and HMBC spectroscopic data as well as chemical studies..
Keywords:Bupleurum falcatum, Apiaceae, Triterpene glycosides, NMR, MS, Chemical studies, Structural characterization

[1.] Nakahara, Y.; Okawa, M.; Kinjo, J.; Nohara, T. Oleanene glycosides of the aerial parts and seeds of Bupleurum falcatum and the aerial parts of Bupleurum rotundifolium, and their evaluation as anti-hepatitis agents. Chem. Pharm. Bull. 2011, 59, 1329-1339.
[2.] Yang, L.Z.; Li, C.; Min, L.X.; Qi, C.; Le, P.R. Cytotoxic saikosaponins from Bupleurum yinchowense. J. Med. Plants Res. 2012, 6, 4409-4415.
[3.] Chaturvedula, V.S.P.; Rhea, J.; Milanowski, D.; Mocek, U., Prakash, I. Two minor diterpene glycosides from the leaves of Stevia rebaudiana. Nat. Prod. Commun. 2011, 6, 175-178.
[4.] Chaturvedula, V. S. P.; Mani, U.; Prakash, I. Diterpene glycosides from Stevia rebaudiana. Molecules. 2011, 16, 3552-3562.
[5.] Chaturvedula, V. S. P.; Prakash, I. A new diterpenoid glycoside from Stevia rebaudiana. Molecules. 2011, 16, 2937-2943.
[6.] Chaturvedula, V. S. P.; Prakash, I. Structures of the novel diterpene glycosides from Stevia rebaudiana. Carbohydr. Res. 2011, 346, 1057-1060.
[7.] Chaturvedula, V. S. P.; Rhea, J.; Milanowski, D.; Mocek, U.; Prakash, I. Two minor diterpene glycosides from the leaves of Stevia rebaudiana. Nat. Prod. Commun. 2011, 6, 175-178.
[8.] Chaturvedula, V. S. P.; Prakash, I. Additional minor diterpene glycosides from Stevia rebaudiana. Nat. Prod. Commun. 2011, 6, 1059-1062.
[9.] Chaturvedula, V.S.P.; Clos, J.F.; Rhea, J.; Milanowski, D.; Mocek, U., DuBois, G.E.; Prakash, I. Phytochemistry Lett. 2011, 4, 209-212.
[10.] Chaturvedula, V. S. P.; Mani, U.; Prakash, I. Structures of the novel α-glucosyl linked diterpene glycosides from Stevia rebaudiana. Carbohydr. Res. 2011, 346, 2034-2038.
[11.] Chaturvedula, V.S.P.; Prakash, I. Curcubitane Glycosides from Siraitia grosvenorii, J. Carbhydr. Chem, 2011, 30, 16-26.

 

Paper Type

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Research Paper

Title

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Role of irbesartan in protection against pulmonary toxicity induced by bleomycin in rats

Country

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Egypt

Authors

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Mariam A. El-Gamal || Sawsan A. Zaitone || Yasser M. Moustafa

Page No.

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38-47

Paper Index

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DOI : 10.9790/3013-034203847  

ANED :: DOI : 05.3013/0342038047

Bleomycin (BLM) is an anti-neoplastic, antibiotic drug that produces dose and time dependant pulmonary fibrosis. Recent studies reported some mechanisms of irbesartan in attenuating lung and skin fibrosis in mice. Therefore, the current study was conducted to examine the effect of irbesartan focusing on angiogenesis and plasminogen activator inhibitor-1(PAI-1) expression as possible mechanisms in protection against BLM-induced lung fibrosis in rats. The effect of irbesartan on the serum and tissue levels of growth factors and mRNA expression of PAI-1 were studied. Oral administration of irbesartan (10, 20 and 40 mg/kg/day) to rats for 21 days, starting from the first day of bleomycin injection (10 mg/kg/day/10 days, i.p.) attenuated the severity of BLM-induced pulmonary fibrosis, enhanced the histopathological features of the lungs, reduced serum transforming growth factor-β1 (TGF-β1) compared to BLM group without any improvement in the survival percentage. In addition, immunohistochemical staining revealed lower expression of angiotensin-II type 1 receptor (AT1) and α-smooth muscle actin (α-SMA) in lung tissues after treatment with irbesartan (20 and 40mg/kg) compared to BLM-treated group. Importantly, irbesartan (10, 20 and 40mg/kg) suppressed the expression of PAI-1 gene in lung tissues while increased both serum level and immunohistochemical staining of vascular endothelial growth factor (VEGF) compared to BLM-treated group. So that, the present study concluded that the ameliorating effect of irbesartan against BLM-induced pulmonary fibrosis in rats involves increasing angiogenesis, reduction of PAI-1 gene expression and modulation of growth factors.
Keywords: Angiogenesis, bleomycin, irbesartan, plasminogen activator inhibitor-1, pulmonary fibrosis.

[1] American Thoracic Society / European Respiratory Society. International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias, Am J Respir Crit Care Med, 165, 2002, 277-304.
[2] American Thoracic Society. Idiopathic Pulmonary Fibrosis: Diagnosis and Treatment International Consensus Statement, Am J Respir Crit Care Med, 161, 2000, 646-664.
[3] H Umezawa, K. Meaeda, T. Takeuchi, and Y. Okami, New antibiotics, bleomycin A and B, J Antibiot (Tokyo), 19(5), 1966, 200-205.
[4] F Chua, J. Gauldie, and G. Laurent, Pulmonary fibrosis: searching for model answers. Am J Respir Cell Mol Biol, 33(1), 2005, 9-13.

[5] M de Gasparo, K. Catt, T. Inagami, J. Wright, and T. Unger, International Union of Pharmacology XXIII. The angiotensin II receptors, Pharmacol Rev, 52(3), 2000, 415- 472.
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[7] Y Kang, Y. Park, B. Kim, S. Han, Y. Jee, K. Han, M. Lee, H. Song, D. Cha, S. Kang, and D. Han, Angiotensin II stimulates the synthesis of vascular endothelial growth factor through the p38 mitogen activated protein kinase pathway in cultured mouse podocytes, J Mol Endocrinol, 36(2), 2006, 377-388.
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Paper Type

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Research Paper

Title

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Physiological Effects Of Melatonin on Leptin, Testosterone and Biochemical Parameters in Albino Rats

Country

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Iraq

Authors

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Sarbast A. Mahmud ||Almas M. R. Mahmud

Page No.

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48-53

Paper Index

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DOI : 10.9790/3013-034204853  

ANED :: DOI : 05.3013/0342048053

The objective for the present study is to investigate of the effects of melatonin (MEL) on serum leptin, testosterone, liver function test parameters in control and pinealectomized (PINx) rats. Thirty seven adult male rats were used in this study. The experimental rats were divided into six groups, and the treatments were continued for six weeks as the following: Group 1: Control rats. Group 2: Sham-operated surgery rats. Group 3: (PINx) rats. Group 4: PINx rats + melatonin (60 mg / Kg diet). Group 5: Melatonin (60 mg / Kg diet). Group 6: Melatonin (120 mg / Kg diet). Reduction in MEL secretion was induced by removing of pineal gland (pinealectomy). Results showed that pinealectomy and MEL treatment at high dose in control rats significantly reduced serum leptin concentration, but MEL at low dose administration in PINx and control rats significantly elevated serum leptin concentration. On the other hand, both doses of MEL significantly decreased serum testosterone concentration. Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activity and malenaldehyde (MDA) levels increased in PINx rats. On the other hand, MEL (60 mg / kg diet) administration decreased serum transaminases activity and MDA level toward normal activity in PINx rats. In conclusion: Melatonin has important roles in the control of leptin production and the regulation of reproductive system (by decreasing testosterone concentration) ,also ,it decreased serum transaminases in PINx rats and this suggests that melatonin has a hepatoprotective role.
Keywords: melatonin, leptin, testosterone, oxidative stress.

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