Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

Moxidectin causes adult worm mortality of human lymphatic filarial parasite Brugia malayi in rodent models

M. Verma, M. Pathak, M. Shahab, K. Singh, K. Mitra, S. Misra-Bhattacharya

. 2014 ; 61 (6) : 561-70.

Language English Country Czech Republic

Document type Journal Article, Research Support, Non-U.S. Gov't

Moxidectin is a macrocyclic lactone belonging to milbemycin family closely related to ivermectin and is currently progressing towards Phase III clinical trial against human infection with the filaria Onchocerca volvulus (Leuckart, 1894). There is a single report on the microfilaricidal and embryostatic activity of moxidectin in case of the human lymphatic filarial parasite Brugia malayi (Brug, 1927) in Mastomys coucha (Smith) but without any adulticidal action. In the present study, the in vitro and in vivo antifilarial efficacy of moxidectin was evaluated on, B. malayi. In vitro moxidectin showed 100% reduction in adult female worm motility at 0.6 μM concentration within 7 days with 68% inhibition in the reduction of MTT (3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide dye) (which is used to detect viability of worms). A 50% inhibitory concentration (IC50) of moxidectin for adult female parasite was 0.242 μM, for male worm 0.186 μM and for microfilaria IC50 was 0.813 μM. In adult B. malayi-transplanted primary screening model (Meriones unguiculatus Milne-Edwards), moxidectin at a single optimal dose of 20 mg/kg by oral and subcutaneous route was found effective on both adult parasites and microfilariae. In secondary screening (M coucha, subcutaneously inoculated with infective larvae), moxidectin at the same dose by subcutaneous route brought about death of 49% of adult worms besides causing sterilisation in 54% of the recovered live female worms. The treated animals exhibited a continuous and sustained reduction in peripheral blood microfilaraemia throughout the observation period of 90 days. The mechanism of action of moxidectin is suggested to be similar to avermectins. The in silico studies were also designed to explore the interaction of moxidectin with glutamate-gated chloride channels of B. malayi. The docking results revealed a close interaction of moxidectin with various GluCl ligand sites of B. malayi.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc15016500
003      
CZ-PrNML
005      
20150512074256.0
007      
ta
008      
150506s2014 xr ad f 000 0|eng||
009      
AR
024    7_
$a 10.14411/fp.2014.068 $2 doi
035    __
$a (PubMed)25651699
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xr
100    1_
$a Verma, Meenakshi $u Division of Parasitology, CSIR-Central Drug Research Institute, Lucknow, Uttarpradesh, India; Academy of Scientific and Innovative Research (AcSIR), Anusandhan Bhawan, New Delhi, India
245    10
$a Moxidectin causes adult worm mortality of human lymphatic filarial parasite Brugia malayi in rodent models / $c M. Verma, M. Pathak, M. Shahab, K. Singh, K. Mitra, S. Misra-Bhattacharya
520    9_
$a Moxidectin is a macrocyclic lactone belonging to milbemycin family closely related to ivermectin and is currently progressing towards Phase III clinical trial against human infection with the filaria Onchocerca volvulus (Leuckart, 1894). There is a single report on the microfilaricidal and embryostatic activity of moxidectin in case of the human lymphatic filarial parasite Brugia malayi (Brug, 1927) in Mastomys coucha (Smith) but without any adulticidal action. In the present study, the in vitro and in vivo antifilarial efficacy of moxidectin was evaluated on, B. malayi. In vitro moxidectin showed 100% reduction in adult female worm motility at 0.6 μM concentration within 7 days with 68% inhibition in the reduction of MTT (3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide dye) (which is used to detect viability of worms). A 50% inhibitory concentration (IC50) of moxidectin for adult female parasite was 0.242 μM, for male worm 0.186 μM and for microfilaria IC50 was 0.813 μM. In adult B. malayi-transplanted primary screening model (Meriones unguiculatus Milne-Edwards), moxidectin at a single optimal dose of 20 mg/kg by oral and subcutaneous route was found effective on both adult parasites and microfilariae. In secondary screening (M coucha, subcutaneously inoculated with infective larvae), moxidectin at the same dose by subcutaneous route brought about death of 49% of adult worms besides causing sterilisation in 54% of the recovered live female worms. The treated animals exhibited a continuous and sustained reduction in peripheral blood microfilaraemia throughout the observation period of 90 days. The mechanism of action of moxidectin is suggested to be similar to avermectins. The in silico studies were also designed to explore the interaction of moxidectin with glutamate-gated chloride channels of B. malayi. The docking results revealed a close interaction of moxidectin with various GluCl ligand sites of B. malayi.
650    _2
$a zvířata $7 D000818
650    _2
$a Brugia malayi $x účinky léků $x metabolismus $7 D017178
650    _2
$a katalytická doména $7 D020134
650    _2
$a chloridové kanály $x chemie $x metabolismus $7 D018118
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a filarióza $x farmakoterapie $x parazitologie $7 D005368
650    _2
$a filaricida $x terapeutické užití $7 D005369
650    _2
$a Gerbillinae $7 D005849
650    _2
$a proteiny červů $x genetika $x metabolismus $7 D015801
650    _2
$a makrolidy $x terapeutické užití $7 D018942
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a Murinae $7 D051189
650    _2
$a vazba proteinů $7 D011485
650    _2
$a konformace proteinů $7 D011487
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Pathak, Manisha $u Division of Parasitology, CSIR-Central Drug Research Institute, Lucknow, Uttarpradesh, India
700    1_
$a Shahab, Mohd $u Division of Parasitology, CSIR-Central Drug Research Institute, Lucknow, Uttarpradesh, India; Academy of Scientific and Innovative Research (AcSIR), Anusandhan Bhawan, New Delhi, India
700    1_
$a Singh, Kavita $u Electron Microscopy Unit, CSIR-Central Drug Research Institute, Lucknow, Uttarpradesh, India
700    1_
$a Mitra, Kalyan $u Academy of Scientific and Innovative Research (AcSIR), Anusandhan Bhawan, New Delhi, India; Electron Microscopy Unit, CSIR-Central Drug Research Institute, Lucknow, Uttarpradesh, India
700    1_
$a Misra-Bhattacharya, Shailja $u Division of Parasitology, CSIR-Central Drug Research Institute, Lucknow, Uttarpradesh, India; Academy of Scientific and Innovative Research (AcSIR), Anusandhan Bhawan, New Delhi, India
773    0_
$w MED00011006 $t Folia parasitologica $x 0015-5683 $g Roč. 61, č. 6 (2014), s. 561-70
856    41
$u https://folia.paru.cas.cz/pdfs/fol/2014/06/11.pdf $y plný text volně přístupný
910    __
$a ABA008 $b A 2854 $c 558 a $y 4 $z 0
990    __
$a 20150506 $b ABA008
991    __
$a 20150507144607 $b ABA008
999    __
$a ok $b bmc $g 1076997 $s 899397
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2014 $b 61 $c 6 $d 561-70 $i 0015-5683 $m Folia parasitologica $n Folia parasitol. $x MED00011006
LZP    __
$b NLK118 $a Pubmed-20150506

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...