Planta Med 2011; 77(14): 1639-1643
DOI: 10.1055/s-0030-1270906
Natural Product Chemistry
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Antiparasitic and Antimicrobial Indolizidines from the Leaves of Prosopis glandulosa var. glandulosa [*]

Aziz Abdur Rahman1 , Volodymyr Samoylenko1 , Melissa R. Jacob1 , Rajnish Sahu1 , Surendra K. Jain1 , Shabana I. Khan1 , Babu L. Tekwani1 , 2 , Ilias Muhammad1
  • 1National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, University, MS, USA
  • 2Department of Pharmacology, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, University, MS, USA
Further Information

Publication History

received Dec. 17, 2010 revised February 15, 2011

accepted February 16, 2011

Publication Date:
07 March 2011 (online)

Abstract

A new indolizidine alkaloid, named Δ 1,6-juliprosopine (1), together with previously known indolizidine analogs (26), was isolated from the leaves of Prosopis glandulosa var. glandulosa, collected from Nevada, USA; while two other known indolizidines, juliprosopine (6) and juliprosine (7), were isolated from P. glandulosa leaves collected in Texas, USA. The structures of compound 1 and 7 were determined using a combination of NMR and MS techniques. Compound 7 exhibited potent antiplasmodial activity against Plasmodium falciparum D6 and W2 strains with IC50 values of 170 and 150 ng/mL, respectively, while 1 was found to be less active (IC50 values 560 and 600 ng/mL, respectively). Both compounds were devoid of VERO cells toxicity up to a concentration of 23 800 ng/mL. The antileishmanial activity of indolizidines was evaluated against Leishmania donovani promastigotes, axenic amastigotes, and amastigotes in THP1 macrophage cultures. When tested against macrophage cultures, the tertiary bases (1, 3, 6) were found to be more potent than quaternary salts (2, 5, 7), displaying IC50 values between 0.8–1.7 µg/mL and 3.1–6.0 µg/mL, respectively. In addition, compound 7 showed potent antifungal activity against Cryptococcus neoformans and antibacterial activity against Mycobacterium intracellulare, while 1 was potent only against C. neoformans and weakly active against other organisms.

1 Part III. For part II, see [8].

References

  • 1 Hilu Y W, Boyd S, Felker P. Morphological diversity and taxonomy of California mesquites (Prosopis, Lepminosae).  Madrono. 1982;  29 237-254
  • 2 Burkhart A. A monograph of the genus Prosopis.  J Arnold Arboretum. 1976;  57 450-525
  • 3 Kay M A. Healing with plants in the American and Mexican West. Tucson; The University of Arizona Press 1996: 221-224
  • 4 Powell A M. Trees and shrubs of Trans-Pecos and adjacent areas. Austin; The University of Texas Press 1998: 177-179
  • 5 Kanthasamy A, Subramanian S, Govindasamy S. Bactericidal and fungicidal effects of Prosopis juliflora alkaloidal fraction.  Indian Drugs. 1989;  26 390-394
  • 6 Ahmad A, Khan K A, Ahmad V U, Qazi S. Antibacterial activity of juliflorine isolated from Prosopis juliflora.  Planta Med. 1986;  52 285-288
  • 7 Ahmad A, Khursheed A K, Sabiha Q, Viqaruddin A. Antifungial activity of some hydrosoluble Prosopis juliflora alkaloids.  Fitoterapia. 1989;  60 86-89
  • 8 Samoylenko V P, Ashfaq M K, Jacob M R, Tekwani B L, Khan S I, Manly S P, Joshi V C, Walker L A, Ilias M. Indolizidine, antiinfective and antiparasitic compounds from Prosopis glandulosa var. glandulosa.  J Nat Prod. 2009;  72 92-98
  • 9 Bero J, Quetin-Leclercq J. Natural products published in 2009 from plants traditionally used to treat malaria.  Planta Medica. DOI: 10.1055/s-0030-1250405 , advance online publication 10 October 2010
  • 10 Ahmad V U, Sultana A, Qazi S. Alkaloids from the leaves of Prosopis juliflora.  J Nat Prod. 1989;  52 497-501
  • 11 Samoylenko V P, Dunbar D C, Jacob M R, Joshi V C, Ashfaq M K, Ilias M. Two new alkylated piperidine alkaloids from western honey mesquite: Prosopis glandulosa Torr. var. torreyana.  Nat Prod Commun. 2008;  3 35-40
  • 12 Ahmad V U, Qazi S J. Studies on the structure of Julifloricine.  J Chem Soc Pakistan. 1985;  7 347-350
  • 13 Mikus J, Steverding D. A simple colorimetric method to screen drug cytotoxicity against Leishmania using the dye Alamar Blue.  Parasitol Int. 2000;  48 265-269
  • 14 Makler M T, Ries J M, Williams J A, Bancroft J E, Piper R C, Gibbins B L, Hinrichs D J. Parasite lactate dehydrogenase as an assay for Plasmodium falciparum drug sensitivity.  Am J Trop Med Hyg. 1993;  48 739-741
  • 15 NCCLS .Reference method for broth dilution antifungal susceptibility testing of yeasts, Vol. 22. Approved standard, 2nd ed. Wayne; National Committee for Clinical Laboratory Standards 2002: 1-51
  • 16 NCCLS .Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically, Vol. 20. NCCLS Document M7-A5. Wayne; National Committee for Clinical Laboratory Standards 2000: 1-58
  • 17 NCCLS .Susceptibility testing of mycobacteria, nocardia, and other aerobic actinomycetes, Vol. 20. Tentative standard M24-T2, 2nd edition. Wayne; National Committee for Clinical Laboratory Standards 2000: 1-81
  • 18 NCCLS .Reference method for broth dilution antifungal susceptibility testing of conidium forming filamentous fungi, Vol. 18. Proposed standard M38-P. Wayne; National Committee for Clinical Laboratory Standards 1998: 1-39
  • 19 Ott-Longoni R, Viswanathan N, Hesse M. Die Konstitution des Alkaloides Juliprosopin aus Prosopis juliflora A. Dc. 176. Mitteilung über organische Naturstoffe.  Helv Chim Acta. 1980;  7 2119-2129
  • 20 Snider B B, Neubert B J. Syntheses of ficuseptine, juliprosine, and juliprosopine by biomimetic intramolecular chichibabin pyridine syntheses.  Org Lett. 2005;  7 2715-2718
  • 21 Daetwyler P, Ott-Longoni R, Schoepp E, Hesse M. Uber Juliprosin, ein weiteres Alkaloid aus Prosopis juliflora A. Dc.  Helv Chim Acta. 1981;  64 1959-1963
  • 22 Babich H, Borenfreund E. Cytotoxicity of T2 toxin and its metabolites with the neutral red cell viability assay.  Appl Environment Microbiol. 1991;  57 2101-2103

1 Part III. For part II, see [8].

Dr. Muhammad Ilias

National Center for Natural Products Research
University of Mississippi

P. O. Box 1848

University, MS 38677

USA

Phone: +1 66 29 15 10 51

Fax: +1 66 29 15 79 89

Email: milias@olemiss.edu

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