-
Je něco špatně v tomto záznamu ?
The in vitro biological activity of Lepidium meyenii extracts
Valentová K, Buckiová D, Kren V, Peknicová J, Ulrichová J, Simánek V.
Jazyk angličtina Země Nizozemsko
Grantová podpora
NJ7463
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Část
Zdroj
NLK
ProQuest Central
od 1997-01-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2000-02-01 do Před 1 rokem
Nursing & Allied Health Database (ProQuest)
od 1997-01-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 1997-01-01 do Před 1 rokem
Public Health Database (ProQuest)
od 1997-01-01 do Před 1 rokem
- MeSH
- bifenylové sloučeniny analýza MeSH
- estrogeny farmakologie MeSH
- financování organizované MeSH
- hepatocyty účinky léků MeSH
- hydraziny analýza MeSH
- krysa rodu rattus MeSH
- kultivované buňky MeSH
- Lepidium chemie toxicita MeSH
- lidé MeSH
- mastné kyseliny analýza MeSH
- nádorové buněčné linie MeSH
- nádory prsu farmakoterapie MeSH
- potkani Wistar MeSH
- preklinické hodnocení léčiv MeSH
- proliferace buněk MeSH
- rostlinné extrakty chemie toxicita MeSH
- steroidy analýza MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- lidé MeSH
- mužské pohlaví MeSH
- zvířata MeSH
The biological activity of methanolic and aqueous extracts from dehydrated hypocotyls of Lepidium meyenii (Brassicaceae, vernacular name "maca"), was studied on rat hepatocytes and human breast cancer MCF-7 cells. The extracts did not exhibit cytotoxicity in hepatocyte primary cultures up to 10 mg/ml as measured by the MTT viability test, and lactate dehydrogenase (LDH) and aspartate aminotransferase (AST) leakage. Moreover, after 72 h, extracts inhibited LDH and AST leakage from the hepatocytes. When hepatocytes were intoxicated by t-butyl hydroperoxide, neither extract prevented oxidative damage. Both extracts showed weak antioxidant activity in the DPPH radical scavenging test with IC(50) values of 3.46 +/- 0.16 and 0.71 +/- 0.10 mg/ml, for aqueous and methanolic extracts, respectively. Thus, the observed effect on spontaneous enzyme leakage is probably mediated through mechanisms other than antioxidant activity. Both methanolic and aqueous extracts have shown estrogenic activity comparable with that of silymarin in MCF-7 cell line. Maca estrogenicity was exhibited in the range from 100 to 200 mug of extract per ml. The findings in the present study show that maca does not display in vitro hepatotoxicity. In contrast, a slight cytoprotective effect, probably not mediated by antioxidant capacity, was noted. Maca extracts exhibited estrogenic activity comparably to the effect of silymarin in MCF-7 cells.
- 000
- 00000naa 2200000 a 4500
- 001
- bmc07525118
- 003
- CZ-PrNML
- 005
- 20130725145538.0
- 008
- 090616s2006 ne e eng||
- 009
- AR
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Valentová, Kateřina, $d 1976- $7 xx0034397
- 245 14
- $a The in vitro biological activity of Lepidium meyenii extracts / $c Valentová K, Buckiová D, Kren V, Peknicová J, Ulrichová J, Simánek V.
- 314 __
- $a Institute of Medical Chemistry and Biochemistry, Faculty of Medicine, Palacký University, Olomouc. valentova@email.cz
- 520 9_
- $a The biological activity of methanolic and aqueous extracts from dehydrated hypocotyls of Lepidium meyenii (Brassicaceae, vernacular name "maca"), was studied on rat hepatocytes and human breast cancer MCF-7 cells. The extracts did not exhibit cytotoxicity in hepatocyte primary cultures up to 10 mg/ml as measured by the MTT viability test, and lactate dehydrogenase (LDH) and aspartate aminotransferase (AST) leakage. Moreover, after 72 h, extracts inhibited LDH and AST leakage from the hepatocytes. When hepatocytes were intoxicated by t-butyl hydroperoxide, neither extract prevented oxidative damage. Both extracts showed weak antioxidant activity in the DPPH radical scavenging test with IC(50) values of 3.46 +/- 0.16 and 0.71 +/- 0.10 mg/ml, for aqueous and methanolic extracts, respectively. Thus, the observed effect on spontaneous enzyme leakage is probably mediated through mechanisms other than antioxidant activity. Both methanolic and aqueous extracts have shown estrogenic activity comparable with that of silymarin in MCF-7 cell line. Maca estrogenicity was exhibited in the range from 100 to 200 mug of extract per ml. The findings in the present study show that maca does not display in vitro hepatotoxicity. In contrast, a slight cytoprotective effect, probably not mediated by antioxidant capacity, was noted. Maca extracts exhibited estrogenic activity comparably to the effect of silymarin in MCF-7 cells.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a bifenylové sloučeniny $x analýza $7 D001713
- 650 _2
- $a nádory prsu $x farmakoterapie $7 D001943
- 650 _2
- $a nádorové buněčné linie $7 D045744
- 650 _2
- $a proliferace buněk $7 D049109
- 650 _2
- $a kultivované buňky $7 D002478
- 650 _2
- $a preklinické hodnocení léčiv $7 D004353
- 650 _2
- $a estrogeny $x farmakologie $7 D004967
- 650 _2
- $a mastné kyseliny $x analýza $7 D005227
- 650 _2
- $a hepatocyty $x účinky léků $7 D022781
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a hydraziny $x analýza $7 D006834
- 650 _2
- $a Lepidium $x chemie $x toxicita $7 D029686
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a rostlinné extrakty $x chemie $x toxicita $7 D010936
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Wistar $7 D017208
- 650 _2
- $a steroidy $x analýza $7 D013256
- 650 _2
- $a financování organizované $7 D005381
- 700 1_
- $a Buckiová, Daniela $7 xx0063935
- 700 1_
- $a Křen, Vladimír $7 xx0070803
- 700 1_
- $a Pěknicová, Jana $7 xx0063931
- 700 1_
- $a Ulrichová, Jitka, $d 1956- $7 ola2002158251
- 700 1_
- $a Šimánek, Vilím, $d 1942- $7 ola200208149
- 773 0_
- $w MED00005739 $t Cell biology and toxicology $g Roč. 22, č. 2 (2006), s. 91-99 $x 0742-2091
- 910 __
- $a ABA008 $b x $y 8
- 990 __
- $a 20090310084605 $b ABA008
- 991 __
- $a 20130725150029 $b ABA008
- 999 __
- $a ok $b bmc $g 661875 $s 518613
- BAS __
- $a 3
- BMC __
- $a 2006 $b 22 $c 2 $d 91-99 $i 0742-2091 $m Cell biology and toxicology $x MED00005739
- GRA __
- $a NJ7463 $p MZ0
- LZP __
- $a 2009-B4/ipme