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

Aspalathin, a C-glucosyl dihydrochalcone from rooibos improves the hypoglycemic potential of metformin in type 2 diabetic (db/db) mice

P. V. Dludla, K. B. Gabuza, C. J. F. Muller, E. Joubert, J. Louw, R. Johnson

. 2018 ; 67 (5) : 813-818. [pub] 20180725

Language English Country Czech Republic

Document type Journal Article

Metformin is the first line therapy of type 2 diabetics, but continued reduction of their life expectancy warrants further investigation into alternative treatment strategies. This study reports on the combinational use of metformin with aspalathin, a C-glucosyl dihydrochalcone with known glucose lowering and antioxidant properties, as an effective hypoglycemic therapy in a type 2 diabetic (db/db) mouse model. When tested as a monotherapy, a low dose of aspalathin (13 mg/kg) showed no effect, while a high dose (130 mg/kg) has already displayed a better potential than metformin in protecting against diabetes associated symptoms in db/db mice. Thus, it remains of interest to determine whether this dihydrochalcone can improve the efficacy of metformin. The results showed that this combination therapy was more effective than the use of metformin as a monotherapy in ameliorating diabetes associated symptoms, including abnormal raised fasting plasma glucose levels, impaired glucose tolerance, as well as excessively increased body weights and fat content. The treated mice also had reduced food and water consumption when compared to untreated controls, with a pronounced effect evident in the last week of treatment. Therefore, this study supports further investigations into the ameliorative effect of combination therapy of metformin and aspalathin against diabetes associated symptoms.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc19004020
003      
CZ-PrNML
005      
20190212140351.0
007      
ta
008      
190124s2018 xr d f 000 0|eng||
009      
AR
024    7_
$a 10.33549/physiolres.933891 $2 doi
035    __
$a (PubMed)30044119
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xr
100    1_
$a Dludla, P. V. $u Biomedical Research and Innovation Platform (BRIP), South African Medical Research Council, Tygerberg, South Africa; Division of Medical Physiology, Faculty of Health Sciences, Stellenbosch University, Tygerberg, South Africa
245    10
$a Aspalathin, a C-glucosyl dihydrochalcone from rooibos improves the hypoglycemic potential of metformin in type 2 diabetic (db/db) mice / $c P. V. Dludla, K. B. Gabuza, C. J. F. Muller, E. Joubert, J. Louw, R. Johnson
520    9_
$a Metformin is the first line therapy of type 2 diabetics, but continued reduction of their life expectancy warrants further investigation into alternative treatment strategies. This study reports on the combinational use of metformin with aspalathin, a C-glucosyl dihydrochalcone with known glucose lowering and antioxidant properties, as an effective hypoglycemic therapy in a type 2 diabetic (db/db) mouse model. When tested as a monotherapy, a low dose of aspalathin (13 mg/kg) showed no effect, while a high dose (130 mg/kg) has already displayed a better potential than metformin in protecting against diabetes associated symptoms in db/db mice. Thus, it remains of interest to determine whether this dihydrochalcone can improve the efficacy of metformin. The results showed that this combination therapy was more effective than the use of metformin as a monotherapy in ameliorating diabetes associated symptoms, including abnormal raised fasting plasma glucose levels, impaired glucose tolerance, as well as excessively increased body weights and fat content. The treated mice also had reduced food and water consumption when compared to untreated controls, with a pronounced effect evident in the last week of treatment. Therefore, this study supports further investigations into the ameliorative effect of combination therapy of metformin and aspalathin against diabetes associated symptoms.
650    _2
$a zvířata $7 D000818
650    12
$a Aspalathus $7 D036903
650    _2
$a chalkonoidy $x aplikace a dávkování $x izolace a purifikace $7 D047188
650    _2
$a diabetes mellitus 2. typu $x krev $x farmakoterapie $7 D003924
650    _2
$a synergismus léků $7 D004357
650    _2
$a flavonoidy $x aplikace a dávkování $x izolace a purifikace $7 D005419
650    _2
$a hypoglykemika $x aplikace a dávkování $x izolace a purifikace $7 D007004
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a metformin $x aplikace a dávkování $7 D008687
650    _2
$a myši $7 D051379
650    _2
$a myši inbrední C57BL $7 D008810
650    _2
$a myši transgenní $7 D008822
655    _2
$a časopisecké články $7 D016428
700    1_
$a Gabuza, K. B. $u Biomedical Research and Innovation Platform (BRIP), South African Medical Research Council, Tygerberg, South Africa
700    1_
$a Muller, C. J. F. $u Biomedical Research and Innovation Platform (BRIP), South African Medical Research Council, Tygerberg, South Africa; Division of Medical Physiology, Faculty of Health Sciences, Stellenbosch University, Tygerberg, South Africa; Department of Biochemistry and Microbiology, University of Zululand, KwaDlangezwa, South Africa
700    1_
$a Joubert, E. $u Plant Bioactives Group, Post-Harvest and Agro-Processing Technologies, Agricultural Research Council (ARC), Infruitec-Nietvoorbij, Stellenbosch, South Africa; Department of Food Science, Stellenbosch University, Stellenbosch, South Africa
700    1_
$a Louw, J. $u Biomedical Research and Innovation Platform (BRIP), South African Medical Research Council, Tygerberg, South Africa; Department of Biochemistry and Microbiology, University of Zululand, KwaDlangezwa, South Africa
700    1_
$a Johnson, R. $u Biomedical Research and Innovation Platform (BRIP), South African Medical Research Council, Tygerberg, South Africa; Division of Medical Physiology, Faculty of Health Sciences, Stellenbosch University, Tygerberg, South Africa
773    0_
$w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 67, č. 5 (2018), s. 813-818
856    41
$u https://pubmed.ncbi.nlm.nih.gov/30044119 $y Pubmed
910    __
$a ABA008 $b A 4120 $c 266 $y 4 $z 0
990    __
$a 20190124 $b ABA008
991    __
$a 20190208102458 $b ABA008
999    __
$a ok $b bmc $g 1375729 $s 1042198
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2018 $b 67 $c 5 $d 813-818 $e 20180725 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
LZP    __
$b NLK118 $a Pubmed-20190124

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...