Abstract
Eight naturally occurring monoindole alkaloids were evaluated in vitro for their ability to inhibit Plasmodium falciparum growth and, in drug combination, to reverse the resistance of a chloroquine-resistant strain of Plasmodium falciparum. None of these indole alkaloids has significant intrinsic antiplasmodial activity (IC50 > 10 μM or 5 μg/ml). Nevertheless, three alkaloids (icajine, isoretuline and strychnobrasiline) did reverse chloroquine resistance at concentrations between 2.5 and 25 μg/ml (IF of 12.82 for isoretuline on W2 strain). The Interaction Factor (IF) equals 2, < 2, or > 2 for additive, antagonistic or synergistic effects of alkaloids on chloroquine inhibition, respectively. Icajine and isoretuline were also assessed in vitro for their mefloquine potentiating activity on a mefloquine-resistant strain of Plasmodium falciparum. Only icajine proved to be synergistic with mefloquine (IF = 15.38).
Key words
Plasmodium falciparum
- chloroquine - mefloquine - indole alkaloid
References
-
1
Martin S K, Oduola A M, Milhous W K.
Reversal of chloroquine resistance in Plasmodium falciparum by verapamil.
Science.
1987;
235
899-901
-
2
Rasoanaivo P, Ratsimamanga-Urverg S, Milijaona R, Rafatro H, Rakoto-Ratsimamanga A, Galeffi C, Nicoletti M.
In vitro and in vivo chloroquine-potentiating action of Strychnos myrtoides alkaloids against chloroquine-resistant strains of Plasmodium malaria.
Planta Medica.
1994;
60
13-6
-
3
Frédérich M, Hayette M P, Tits M, De Mol P, Angenot L.
In vitro activities of Strychnos alkaloids and extracts against Plasmodium falciparum
.
Antimicrobial Agents and Chemotherapy.
1999;
43
2328-31
-
4
Frédérich M, Tits M, Hayette M P, Brandt V, Penelle J, De Mol P, Llabres G, Angenot L.
10’-Hydroxyusambarensine, a new antimalarial bisindole alkaloid from the roots of Strychnos usambarensis
.
Journal of Natural Products.
1999;
62
619-21
-
5
Frédérich M, De Pauw-Gillet M C, Llabres G, Tits M, Hayette M P, Brandt V, Penelle J, De Mol P, Angenot L.
New antimalarial and cytotoxic sungucine derivatives from Strychnos icaja roots.
Planta Medica.
2000;
66
262-9
-
6
Angenot L, Tits M.
Isolement d’un nouvel alcaloïde et d’un triterpénoïde à partir du Strychnos henningsii du Zaïre.
Planta Medica..
1981;
41
240-3
-
7
Angenot L, Belem-Pinheiro M L, Imbiriba da Rocha A F, Poukens-Renwart P, Quetin-Leclercq J, Warin R.
An indolinic cryptoalkaloid from Strychnos mattogrossensis
.
Phytochemistry.
1990;
29
2746-9
-
8
Bisset N G, Das B, Parello J.
Alkaloids from the leaves of Strychnos icaja Baill.
Tetrahedron.
1973;
29
4137-48
-
9
Brandt V, Tits M, Geerlings A, Frédérich M, Penelle J, Delaude C, Verpoorte R, Angenot L.
Beta-carboline glucoalkaloids from Strychnos mellodora
.
Phytochemistry.
1999;
51
1171-6
-
10
Tavernier D, Anteunis M JO, Tits M, Angenot L.
The 1H NMR spectra of the Strychnos alkaloids retuline, isoretuline and their N-deacetyl compounds.
Bulletin de la Société Chimique Belge.
1978;
87
595-607
-
11
Frédérich M, Tits M, Angenot L.
Qualitative and quantitative evaluation of bisindole usambarane alkaloids in Strychnos usambarensis roots by high performance liquid chromatography-diode-array.
Phytochemical Analysis.
1998;
9
63-6
-
12
Gadi-Biala R, Tits M, Wauters J N, Angenot L.
A new HPLC method for the assay of alkaloids in Strychnos nux-vomica and Strychnos ignatii
.
Fitoterapia.
1996;
67
163-5
-
13
Trager W, Jensen J B.
Human malaria parasites in continuous culture.
Science.
1976;
193
673-5
-
14
Desjardins R E, Canfield C J, Haynes J D, Chulay J D.
Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique.
Antimicrobial Agents and Chemotherapy.
1979;
16
710-8
-
15
Mirovsky P, Gay F, Bustos D, Mazier D, Gentilini M.
Cloning of a fresh isolate of Plasmodium falciparum and drug sensitivity of the clones.
Transactions of the Royal Society of Tropical Medicine and Hygiene.
1990;
84
511-5
-
16
Berenbaum M.
What is synergy?.
Pharmacological Reviews.
1989;
41
93-141
-
17
Loewe S.
The problem of synergism and antagonism of combined drugs.
Arzneimittelforschung.
1953;
3
285-90
-
18
Frappier F, Jossang A, Soudon J, Calvo F, Rasoanaivo P, Ratsimamanga-Urveg S ,. et al .
Bisbenzylisoquinolines as modulators of chloroquine resistance in Plasmodium falciparum and multidrug resistance in tumor cells.
Antimicrobial Agents and Chemotherapy.
1996;
40
1476-81
-
19
Bonjean K A, De Pauw-Gillet M C, Quetin-Leclercq J, Angenot L, Bassleer R J.
In vitro cytotoxic activity of two potential anticancer drugs isolated from Strychnos: strychnopentamine and usambarensine.
Anticancer Research.
1996;
16
1129-37
-
20
Peters W, Robinson B L.
The chemotherapy of rodent malaria. XLVI. Reversal of mefloquine resistance in rodent Plasmodium
.
Annals of Tropical Medicine and Parasitology.
1991;
85
5-10
-
21
Oduola A M, Omitowoju G O, Gerena L, Kyle D E, Milhous W K, Sowunmi A, Salako L A.
Reversal of mefloquine resistance with penfluridol in isolates of Plasmodium falciparum from south-west Nigeria.
Transactions of the Royal Society of Tropical Medicine and Hygiene.
1993;
87
81-3
Michel Frédérich
Laboratoire de Pharmacognosie
Institut de Pharmacie
Université de Liège
Avenue de l’hôpital 1
CHU du Sart Tilman, B36, tour 4
4000 Liège
Belgium
eMail: M.Frederich@ulg.ac.be
Fax: +32 4 366 43 32