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XI. Woorkshop<br />

of Physsical<br />

Chemists and a Electrochemmists´11<br />

skeleetal<br />

muscullature<br />

and intense paiin.<br />

Death occurs o after r one hourrs<br />

through respiratoryy<br />

parallysis<br />

or heaart<br />

failure [3 3, 9-11].<br />

However, , some studies<br />

have demonstra ated also phenolic<br />

coonstituents,<br />

especiallyy<br />

flavoonol<br />

and hyydroxyphen<br />

netyl glycoosides<br />

with antioxidan nt propertiees<br />

[12-14]. Flavonoidss<br />

havee<br />

been fouund<br />

in some<br />

subspeecies<br />

of Aconitum A napellus n – A. napel llus subsp. .<br />

neommontanum<br />

(Wulfen) ) Bayer (flowers - querceti in 7-O-(66-trans-caff<br />

feoyl)-beta-<br />

glucoopyranosyll-(1,3)-alpha-rhamnoppyranoside-3-O-beta-g<br />

glucopyrannoside,<br />

kaem mpferol7- O-(66-trans-cafffeoyl)-beta-glucopyrannosyl-(1,3)-<br />

-alpha-rham mnopyranooside-3-O-b<br />

beta<br />

glucoopyranosidde<br />

and kae empferol 77-O-(6-tran<br />

ns-p-coumaroyl)-beta-glucopyran<br />

nosyl-(1,3)-<br />

alphaa-rhamnoppyranoside<br />

3-O-beta-gglucopyrano<br />

oside together t<br />

with beta-3,4-<br />

dihyydroxyphennethyl<br />

beta a-glucopyraanoside)<br />

an nd A. nape ellus subspp.<br />

tauricum m (Wulfen) )<br />

Bayeer,<br />

species distributed<br />

in Easteern<br />

Alps and a southe ern Carpatthians<br />

(3-O O-(6-trans-<br />

caffeeoyl)-beta-gglucopyranosyl-(1,2)-bbeta-glucop<br />

pyranoside-7-O-alphaa-rhamnopy<br />

yranoside,<br />

kaemmpferol<br />

3-O-(6-trans<br />

s-caffeoyl)-bbeta-glucop<br />

pyranosyl-( (1,2)-beta-gglucopyran<br />

noside-7-O-<br />

alphaa<br />

-rhamnoopyranosid<br />

de, quercettin<br />

3-O-(6 6-trans-p-co oumaroyl)-beta-gluco<br />

opyranosyl-<br />

(1,2) -beta-glucoopyranoside<br />

e-7-O-alphha-rhamnop<br />

pyranoside aand<br />

beta-3,4-<br />

dihyydroxyphennethyl<br />

beta-glucopyrannoside)<br />

[15 5, 16]. Flav vonoids havve<br />

been fou und also inn<br />

other<br />

members of Aconitu um genus [117].<br />

Fig.<br />

1: The most<br />

import tant diterppene<br />

alkalo oids of Aco onitum nap apellus aggr regate. 1 -<br />

napellinne,<br />

Fig. 2: aconitinne<br />

- (R<br />

hypacon<br />

1 = -<br />

nitine (R1 -CH2CH3, R<br />

= CH3, R2 R<br />

= H<br />

2 = -OH), mesakonit tine (R<br />

H)<br />

1 = --CH3,<br />

R2 = -OH) andd<br />

Plants of Aconitum genus are uused<br />

in tra aditional Ch hinese meddicine<br />

after processingg<br />

to ddecompose<br />

toxic alka aloids to the less toxic t deriv vatives andd<br />

for prep paration off<br />

hommeopathic<br />

prreparations<br />

s [18-20].<br />

2. EXPERIMMENT<br />

Plant maaterial<br />

(roo ots, stems, leaves) was w collecte ed in the botanical garden off<br />

Univversity<br />

of VVeterinary<br />

and a Pharmmaceutical<br />

University U Brno. For tthe<br />

anatom mical study, ,<br />

transsversal,<br />

raddial<br />

and tan ngential hannd-made<br />

se ections wer re used. Foor<br />

the visua alization off<br />

ligniified<br />

plant ttissues,<br />

ethanolic<br />

(50 % %, v/v) mix xture of acid<br />

fuchsinee<br />

and malac chite greenn<br />

(bothh<br />

1%, w/ww;<br />

Sigma-Al ldrich, USAA)<br />

was use ed. Sections s were stainned<br />

for fou ur minutess<br />

and aafter<br />

it wasshed<br />

with acidic a ethannol<br />

(60 %, v/v, v with 37 7% hydrochhloric<br />

acid 0.1 %, v/v, ,<br />

- 25 -<br />

Brnoo

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