Professional Documents
Culture Documents
Journal of Ethnopharmacology,
17 (1986) 37-64
Elsevier Scientific Publishers Ireland Ltd.
PHARMACOLOGY
OF LEMONGRASS
(CYMBOPOGON
CZTRATUS
STAPF). I. EFFECTS OF TEAS PREPARED FROM THE LEAVES ON
LABORATORY
ANIMALS*
862, 04023
April 30,1986)
Summary
Cymbopogon
citrutus is one of the most used plants in Brazilian folk
medicine for the treatment of nervous and gastrointestinal disturbances. It
is also used in many other places to treat feverish conditions. The usual way
to use it is by ingesting an infusion made by pouring boiling water on fresh
or dried leaves (which is called abafado in Portuguese). Abafados obtained
from lemongrass harvested in three different areas of Brazil (Ceara, Minas
Gerais and Slo Paulo States) were tested on rats and mice in an attempt to
add experimental confirmation to its popular medicinal use. Citral, the main
constituent of the essential oil in Brazilian lemongrass, was also studied for
comparison. Oral doses of abafados up to 40 times (CL,,) larger than the
corresponding dosage taken by humans, or of 200 mg/kg of citral, were
unable to decrease body temperature of normal rats and/or rats made hyperthermic by previous administration of pyrogen. However, both compounds
acted when injected by intraperitoneal route. Oral administration of doses
C20 -CloOof abafados and 200 mg/kg of citral did not change the intestinal
transit of a charcoal meal in mice, nor did it decrease the defecation scores
of rats in an open-field arena. Again, by intraperitoneal route both compounds were active. The possible central nervous system depressant effect
of the abafados was investigated by using batteries of 12 tests designed to
detect general depressant, hypnotic, neuroleptic, anticonvulsant and anxiolytic effects. In all the tests employed, oral doses of abafados up to C,,, or
of citral up to 200 mg/kg were without effect. Only in a few instances did
*This work was aided by Central de Medicamentos (CEME) and AssociacZo Fundo de
Incentive I Psicofarmacologia (AFIP).
0378-8741/86/$10.15
o 1986 Elsevier Scientific Publishers Ireland Ltd.
Published and Printed in Ireland
38
intraperitoneal
doses demonstrate
effects. These data do no lend support to
the popular oral therapeutic use of lemongrass to treat nervous and intestinal
ailments and feverish conditions.
Introduction
Cy~~o~ogo~
citrutus Stapf. (family Gramineae), lemongrass in English,
popularly known in Brazil as capim-cidr&o or cupim-sunto, is widely employed in Brazilian folk medicine, Prepared as a tea or abafado, it is frequently used as a sedative (calmative)
and hypnotic, but also as an analgesic, anti-emetic, antispasmodic
and to treat other stomach and intestinal
ailments (van den Berg, 1980; Matos et al., 1982; Nogueira, 1983; Paviani,
1964).
The medicinal use of lemongrass is not restricted to Brazil. On Mauritius
Island and on the Malay Peninsula it is recommended
against the common
cold, pneumonia, fever and gastric problems (Fook, 1980); in Nigeria as an
antipyretic and for its stimulant and antispasmodic effects (Olaniyi et al.,
1975); in Angola and India it is considered as an antitussigen, anti-emetic,
antiseptic and antirheumatic
(Alves et al., 1960); in Indonesia it is employed
to help digestion and as a diuretic and sudorific (Hirschhorn, 1983).
Substances extracted from lemongrass are also used in medicine. In India
its essential oil is used to treat gastrointestinal
problems (Alves et al., 1960)
and geraniol, one of the constituents
of the essential oil, is prescribed as an
asthmolytic
in China (Peigen, 1983).
The concentration
of the essential oil fraction obtained from lemongrass
varies from 0.2% up to 3% of the fresh plant (Alves et al., 1960); a sample
from South Brazil yielded 0.28% of essential oil (Silva and Bauer, 1971). The
essential oil fraction is composed of many compounds:
alcohols, aldehydes,
ketones, acids, esters and other terpenes and sesquiterpenes.
In the essential
oil obtained from the plant grown in the Phillipines, Somalia, India, Ceylon,
Angola and Congo, the main component
is citral (a mixture of neral and
geranial) which constitutes
30--80% of the oil fraction (Abegaz and
Yohannes, 1983; Oliveros-Belardo
and Aureus, 1980; Rabha et al., 1980;
Sylva, 1980; Vale, 1964); in the Ethiopian essential oil geraniol is the main
constituent
(Abegaz and Yohannes, 1983). In two samples of essential oil
obtained from lemongrass of South (Rio Grande do Sul State) and Southeast (Sdo Paulo State) Brazil, citral was present as the main component
(86% and 48%) (Silva and Bauer, 1971; Liberalli et al., 1946).
Despite the ubiquitous medicinal use of lemongrass there is a great paucity
of pharmacological
research on the plant. A survey of Biological Abstracts
from 1954 to 1983, revealed only two articles, one dealing with the sedative
effects of the essential oil from Cymbopogon
nardus (Kokate et al., 1972)
and the other describing the anti-asthmatic
properties of a component
of
Cym~opogo~
distuns (Huang et al., 1976). Similarly, a survey of the Cumu-
39
luted Index Medicus from 1960 to 1982 disclosed only two references on an
antispasmodic principle present in Cymbopogon proximus (Abdel-Moneim
et al., 1969; Radwan, 1975).
The present paper deals with the pharmacological effects of the tea of
Cymbopogon citratus on laboratory animals. For comparison purposes citral
was also used. It was decided to investigate the popular preparation (abafado)
rather than chemical entities obtained from C~mbopogon citrates in an
attempt to directly confirm the folk medicinal use of the plant.
To obtain data aiming to confirm the traditional therapeutic use in gastrointestinal ailments, experiments on charcoal intestinal transit in mice anr
defecation of rats in an open-field apparatus were performed. To study the
eventual antipyretic properties of lemongrass, the body temperature of rats
was measured. To evaluate the possible depressant effect on the central
nervous system the following experiments were carried out: measurements
of spontaneous motor activity in mice, grooming and rearing of rats in the
open-field and rota-rod performance of mice, were used to given an indication of general depressant activity; measurements of the sleep-wakefulness
cycle of rats (electroencephaphalography)
and potentialization of barbiturate sleeping-time of mice were used to study hypnotic activity; measurements of catatonic behavior and palpebral ptosis of rats and blockade of
stereotyped behavior induced by apomorphine in rats were carried out to
assess eventual neuroleptic effect; meas~ements of neophobia reaction
and punished responses in rats were used to check a possible anxiolytic
effect; and, finally, measurements of electroshock- and pentylenetetrazolinduced convulsions were made to assess any anticonvulsant effect.
Materials and methods
Plant material
Samples of C~mbopogon citratus Stapf. from the state of CearL (Northeast Brazil), Srj,o Paul0 (Southeast Brazil) and Minas Gerais (Southeast) were
harvested from July to November. The specimens were classified by botanists from the local universities.
The essential oil fraction of lemongrasses from Sao Paulo and Ceari
revealed 46.6% and 70.9% citral and 36.7% and 16.0% myrcene, respectively
(Matos et al., 1984, and unpublished data). The citral from the Cear& sample
was composed of 44.2% neral and 55.8% geranial; that of Sio Paulo had 48%
and 52%, respectively (Matos et al., 1984).
The doses administered to mice and rats were based on the amounts
ingested by human beings. In Brazil the abafados are usually prepared from
two fresh leaves finely minced with scissors or from 2 g of dried material,
with 150 ml of tap water. This corresponds to about 2.0 ml abafado/kg body
wt. Leaves were dried in an oven at 37-40C for 3 days resulting in a water
loss of 67-78%.
For administration to mice an abu~udo I was prepared by pouring 150 ml
40
methods
tests were performed
or intraperitoneally)
either
vehicle, doses Cl0 to CGOof abafados I, II and III of lemongrass from Sdo
Paulo and CearS or 100 and 200 mg/kg of citral. The colonic temperature,
measured by inserting the sensor probe of a digital thermometer
5-6 cm
into the colon was recorded before drug treatment (time 0) and 1, 2, 3 and
4 h after drug administration.
In a second experiment,
groups of six rats each were previously injected
with 10 mg/kg of the pyrogen agent from E. coti, Two hours later when the
rats temperature
was beginning to rise, abafudos were given to the animals
orally and the temperature
was again recorded 1, 2 and 4 h later.
Intestinal transit in mice
Twenty-four-hour
fasted mice, in groups of 10 animals each, received
either vehicle, abilfudo I or citral through oral or i.p. routes. Thirty or
60 min later (see Table 2) they were given orally 0.35 ml of an aqueous
suspension of 10% charcoal in 5% gum acacia (Turner, 1965). Fifteen
minutes later the animals were killed by cervical dislocation and the small
intestines removed. The distance the charcoal had transited from the pylorus
was measured and expressed as the percentage of the total length of the
small intestines.
Open-field behavior
The open field consisted of a white painted arena of plywood measuring
48 X 28 X 20 cm in diameter with three 60 W lamps and three loudspeakers
producing a constant noise of 76 decibels. The floor of the arena was divided
into several units by black painted lines (for details see Masur, 1972).
Groups of eight rats each were treated with several abafudos from Sao
Paulo lemongrass or with citral. One hour after oral administration
or 30 min
after i.p. injection each rat was placed in the center of the arena and defecation (number of fecal boluses eliminated), ambulation (number of floor units
entered) and rearing (number of times the rat stood up) were recorded for
3 min.
Rota-rod test
Groups of 10 previously selected mice received various doses of abafados
or citral either by oral or intraperitoneal
routes, as can be seen in Table 4.
The apparatus consisted of a bar, with a diameter of 2.5 cm subdivided into
five compartments
by disks 25 cm in diameter (Dunham and Miya, 1957).
The bar rotated at a constant speed of 12 rev./min. Pre-selection of animals
was done on the experiments
day by eliminating those mice which did not
remain on the bar for two consecutive periods of 1 min.
One hour after the drug administration
the animals were retested and the
time they remained on the rotating bar, with a maximum of 60 s, were
recorded.
Span tuneous motor activity
Abafado I made from dried leaves from Sso Paul0 and Ceari was used.
42
Abafado III from SBo Paulo was also studied. Vehicle and citral groups were
included for comparison purposes. For each dose and drug 10 mice were
employed. Spontaneous motor activity was recorded by means of 10 identical photocell cages, each measuring 25 X 40 X 25 cm and crossed by three
light-beams.
The mice were placed individu~ly in the cages 5 min after i.p. or 30 min
after oral drug administration, and the number of light-beam interruptions
was recorded for the next 30 min.
Barbiturate sleeping-tide
Groups of 10 mice each were administered orally or i.p. either with
vehicle (water), doses from CsOto C208of abafados I, II and III prepared
from dried leaves from Sao Paulo, Minas Gerais and Ceara or with 100 mg/
kg of citral. Thirty minutes later the animals pretreated with the abafados
or with citral received, respectively, 50 or 40 mg/kg of sodium pentob~bit~
intraperitoneally. After the barbiturate injection the sleeping-time (time
interval between loss and recuperation of the righting reflex) was recorded in
minutes. The criterion for recuperation of the righting reflex was fixed such
that the animals had to regain their normal posture three consecutive times.
43
Water
Fresh leaves
Dried leaves
Water
Citral
Citral
Citral
significantly
---
I
I
II
III
Abafado I
A bafado I
Abafado
Abafado
A bafado
Abafado
Preparation
from vehicle-treated
S&o Paulo
SIo Paulo
leaves
leaves
leaves
leaves
*Differs
Sio Paulo
Ceari
Slo Paulo
Sio Paulo
Water
Dried
Dried
Dried
Dried
Source
Naterial
i.p.
orat
i.p.
i.p.
i.p.
i.p.
i.p.
2 ml/kg
200 mg/kg
100 mg/kg
200 mg/kg
8 ml/kg
c 20
C Zil
oral
oral
oral
oral
Route
AND DRIED
8 ml/kg
C I:0
C 2*
C *o
C .o
Dose
TABLE 7
t 0.44
+_0.19
r 0.29
t 0.33
?r 0.26
analysis
r
t
i
*
0.26
0.29
0.24
0.19
of variance
38.3
37.7
37.1
37.8
37.9 r 0.48
38.2 * 0.47
38.2 i: 0.25
38.1
38.2
38.0
38.4
37.5
Oh
t
t
+
5
t
0.27
I.38
0.38
1.38
0.23
followed
37.6
36.9
37.1
36.2
t
r
t
c
f 0.13
t 1.50
?: 0.14
+ 1.37
f 0.28
37.3
36.9
36.8
35.4
t-test).
+ 0.16
t 0.83
r 0.74
t 0.60*
37.4 c 0.40
36.2 i 0.64*
35.8 + 0.79*
37.6
36.6
37.7
36.7
37.8
2h
by Students
0.42
0.72
0.50
0.26*
37.5 f 0.18
37.2 L 0.48
36.8 ?: 0.42
37.7
36.7
37.9
36.8
37.5
lh
ON BODY
f
t
t
*
f
0.17
1.63
0.25
0.42
0.20
37.4
37.3
37.1
36.8
+
5
t
+
0.22
0.36
0.52
0.49
37.7 f 0.36
38.0 +_0.26
37.5 + 0.25
37.7
37.9
37.7
37.3
37.0
4h
AND OF CITRAL
(C + S.D.) before
OF LEMONGRASS
Temperature
LEAVES
46
On the other hand, when doses CzO of u~u~~dos I obtained either from
fresh or dried leaves of lemongrass from Sdo Paulo were given through
intraperitoneal
route, a statistically significant decrease in temperature
was
obtained 2 h after the injections (lines 7 and 8).
Citral (200 mg/kg) by oral route and 100 mg/kg i.p. did not significantly
affect the temperature;
only 200 mg/kg i.p. was effective in doing so in the
first 2 h after administration
(last 4 lines of Table 1).
Finally, the ~~u~~do I obtained from the dried feaves of Sgo Paulo was
unable to counteract the fever induced in the rats by the pyrogen of E. co&
Thus, 1 and 2 h after orally administering a dose C&, (or 4 h after the injection of 10 mg/kg of the pyrogen), the temperature
of the rats were 38.7 +
0.48C and 38.3 + 0.2OC, respectively. These results did not differ from the
values of the control group, 38.1 + 0.37 and 38.5 f 0.35, respectively,
1 and 2 h after vehicle.
~nt~sti~a~ transit
According to the first 6 lines of Table 2, oral doses CsO and Ctoo of
abafudo I obtained from fresh or dried leaves of Iemongrass from Sgo Paulo
did not alter the intestinal activity of mice. Thus, the charcoal meal travelled
from 55% to 73% of total small intestines whether the previous treatment had
been water or any of the abafados. However, doses CloO of the abafudos from
Stjo Paulo and CearG administered
intraperitoneally
(lines 7 and 8 of
Table 2) drastically reduced in~stin~
transit. Similar results were obtained
with citral. Through the oral route, 100 and 200 mgfkg did not modify the
intestinal activity (lines 9-11) although the same doses when administered
intraperitoneally,
produced a clear reduction in intestinal transit (last 4 lines
of Table 2).
Open-field
behavior
As can be seen in the first three lines of Table 3, oral doses CzO of abafado
I slightly reduced defecation
but the difference did not reach statistical
significance. A replication of this experiment (lines 4 -7 of Table 3) again
showed the same non-significant
decrease in defecation produced either by
doses Czo of abafadas I and II or by intraperitoneal
injection of dose Cl0 of
abafado I. One hundred mg/kg of citral by oral route was also unable to
significantly reduce defecation in rats. However, a marked decrease was
noticed when citral was given by the intraperitoneal
route.
As far as ~bulation
is concerned, as seen in Table 3, none of the above
treatments was effective in modifying it. Rearing was affected only by the
i.p. injection of 100 mg/kg of citral.
Rota-rod
Abafado
I (first 7 lines of Table 4) from fresh leaves from Sao Paulo and
Minas Gerais did not alter the performance
of mice on the rotating bar,
when administered either by oral or i-p. routes or in doses 50 times larger
Sio Paul0
Slo Paul0
SIo Paul0
S&o Paul0
Cearl
Cearl
Water
Fresh leaves
Dried leaves
Water
Fresh leaves
Dried leaves
Dried leaves
Dried leaves
Water
Citral
Citral
Water
Citral
Citral
Citral
40 ml/kg
C I0
C IO
C ,O
C I no
20 ml/kg
100 mg/kg
200 mg/kg
20 ml/kg
25 mg/kg
100 mg/kg
200 mg/kg
60
60
60
30
30
60
60
60
30
30
30
30
I
I
I
I
C 50
30
Abafado
Abafado
Abafado
Abafado
20 ml/kg
C 50
30
30
Abafado
Abofado
Dose
Minutes
elapsed between
drug and
charcoal
Preparation
66.8 + 18.8
71.0 t 14.0
73.0 f 12.8
oral
oral
oral
71.6
55.8
21.3
18.0
+ 19.0
t 23.7
+_ 5.3**
* 2.9**
66.8 f 6.8
69.1 2 11.2
59.6 + 19.5
oral
oral
oral
i.p.
i.p.
i.p.
i.p.
66.2
63.4
55.6
28.0
25.6
oral
oral
oral
i.p.
i.p.
+ 12.3
* 12.2
r 13.2
f- 8.1*
+_ 7.5**
Intestinal transit?
Route
a Percent of total length of small intestine travelled by the charcoal meal. Values are mean f S.U.
* Differs significantly from vehicle treated mice (*P < 0.01; **P < 0.001; one-way analysis of variance followed by Students f-test).
Source
Material
EFFECT OF ABAFADO
TRANSIT IN MICE
TABLE 2
A bafudo
A bafado
A bafado I
Abafudo
II
Abafado I
Water
Fresh leaves
Dried leaves
Water
Fresh leaves
Dried leaves
Dried leaves
Water
Citral
Citral
i.p.
oral
i.p.
i.p.
c 10
1 ml/kg
100 mg/kg
100 mg/kg
oral
oral
oral
oral
oral
oral
Route
8 ml,kg
C
C:::
8 ml/kg
C 20
C 70
Dose
+ 2.2
+ 2.2
3.0 % 2.4
0.1 f 0.3*
4.4
2.3
4.4 +_0.8
3.1 * 0.7
2.8 * 1.7
5.0 % 2.6
2.9 +_2.4
3.5 f 2.2
Defecation
(mean c S.D.)
+_12.3
+ 16.0
36.8 + 16.5
36.9 f 11.7
47.8
30.1
45.3 * 21.0
44.0 i 10.3
39.2 f 14.9
48.4 + 9.5
43.4 * 12.7
45.8 * 11.4
Ambulation
(mean + S.D.)
5.3
18.0 + 11.6
8.6 t 6.0
7.1 + 4.7*
9.8
16.0 f- 7.1
18.0 r 6.5
14.2 f_ 9.4
17.0 + 7.8
15.1 f. 4.8
11.2 -t 6.7
Rearing
(mean + SD.)
*Differs significantly from vehicle-treated rats (*P $ 0.05; one-way analysis of variance followed bv Students t-test).
I
I
Preparation
FROM LEMONGRASS
Material
EFFECTS OF ABAFADOS
RATS
TABLE 3
19
OF ABAFADOS
leaves
leaves
leaves
leaves
leaves
leaves
leaves
leaves
leaves
leaves
leaves
Water
Dried
Dried
Dried
Dried
Dried
Dried
Dried
Water
Dried
Dried
Dried
Dried
Water
Citral
Citral
Citral
leaves
leaves
leaves
leaves
leaves
leaves
Water
Fresh
Fresh
Fresh
Fresh
Fresh
Fresh
Material
Paul0
Paul0
Paula
Paul0
Abafado
A bafado
A bafado
Abafado
Sio
SZo
Sio
Sio
Abafado
Abafado
A bafado
Abafado
A bafado
Abafado
Abafado
Sio Paul0
Minas Gerais
CearSl
Ceari
Sio Paul0
SHo Paul0
S&o Paul0
Abafado
Abafado
Abafado
Abafado
Abafado
Abafado
Sio Paul0
Sio Paul0
Sit0 Paul0
Minas Gerais
SHo Paul0
Sio Paul0
Preparation
FROM LEMONGRASS
EFFECTS
TABLE 4
III
III
III
III
I
I
I
I
II
I
I
I
I
I
I
I
I
i.p.
oral
oral
i.p.
i.p.
oral
oral
i.p.
i.p.
20 ml/kg
100 mg/kg
50 mg/kg
100 mg/kg
oral
oral
oral
oral
oral
oral
i.p.
i.p.
oral
oral
oral
oral
oral
i.p.
i.p.
Route
ON ROTA-ROD
40 ml/kg
c 10.
C 201
C 104
C 201
Dose
AND OF CITRAL
57.7
55.5
50.6
44.8
47.0
53.3
52.5
38.6
26.7
53.5
50.6
57.1
54.2
50.6
55.0
54.3
51.8
58.7
59.0
51.9
42.4
49.9
50.1
46.0
18.0
17.7
16.9
20.3
21.7
i 5.7
t 6.9
+ 16.2
* 23.5
t
f
t
*
+
f 11.5
t 14.2
t 7.6
t 13.5
L 16.5
r 8.2
f. 10.8
t 13.6
* 4.1
+ 3.9
t 13.2
+_20.1
i- 6.2
t. 16.7
t 18.5
Performance
(s r SD.)
PERFORMANCE
on the rota-rod
OF MICE
cxi
I
I
I
I
III
I
20
50
100
25
50
100
ml/kg
mglkg
mg/kg
mg/kg
mg/kg
mg/kg
C,
C,
C I0
c )111,
C,%,
C Irt0
i.p.
oral
oral
i.p.
i.p.
i.p.
oral
oral
oral
oral
oral
oral
oral
Route
t 118
k 102
+ 81
_c140
+ 127
r 108
+ 122
+ 121
329 f 87
292 r. 79
235 + 87
260 c 112
185?
87*
82 r 50**
280
240
264
290
278
230
230
235
Mean f&D.)
of light-beam inte~uptions
*Differs significantly from vehicle-treated mice (*P Q 0.05; **P G 0.02; one-way analysis of variance followed by Students t-test).
Water
Citral
Citral
Citral
Citral
Abafado
Abafado
A bafado
A bafado
A bafado
Abafado
SHo Paul0
Slio Paul0
SPo Paul0
SIo Paul0
SHo Paul0
Cearsi
20 ml/kg
40 ml/kg
Water
Water
Dried leaves
Dried leaves
Dried leaves
Dried leaves
Dried leaves
Dried leaves
Dose
Preparation
Source
Material
EFFECTS OF ABAFADOS
ACTIVITY OF MICE
TABLE 5
I
II
III
III
I
1
I
Stio Paul0
Go Paul0
SIo Paul0
Sio Paul0
Sio Paul0
St%0Paul0
Minas Cerais
Cead
Cearl
Source
20 ml/kg
100 mgikg
100 mg/kg
20 ml/kg
C 10.
C 208
Dose
oral
oral
i.p.
i.p.
i.p.
i.p.
oral
oral
oral
oral
oral
oral
oral
oral
Route
f 31.3
L 36.0
i 27.2
?: 22.3
+ 20.0
t 23.6
+ 22.4
F 15.1
22.2 t 19.7
24.3 t 21.7
68.9 ?: 26.0*
46.5 r 16.2
52.2 t 18.1
53.8 t 15.2
44.1
66.0
44.8
43.2
41.4
42.9
33.8
32.9
Sleeping-time
(min t S.D.)
*Differs significantly from vehicle-treated group (P G 0.02; one-way analysis of variance followed by Students t-test).
Water
Citral
Citral
Water
Abafado III
A bafudo III
Water
Abafado
Abafado
A bafado
Abafudo
Abafado
Abafado
Abofado
Material
or preparation
EFFECT OF ABAFADOS
TIME OF MICE
TABLE 6
SLEEPING-
f
f
5
+
*
*
22
10
17
19
22
19
343 5 73
73
59
52
55
53
50
f 17
+ 18
* 21
+_23
+ 17
+ 14
359 t 68
72
66
50
65
64
42
+ 19
t. 11
+ 17
5 17
t 18
c 15
315 + 68
66
53
48
52
48
48
Water
Water
A bafado
Total sleep
*Differs significantly from water treatment (P < 0.05; Students f-paired test).
b-12
o-2
2-4
4-6
6-8
8-10
10-12
Time interval
after drug
administration
th)
f
t
t
r
f.
2
14
18
18
20
17
12
325 + 61
65
57
47
59
58
39
A bafado
TABLE 7
+ 6.2
r 3.6
+ 1.9
+_1.9
+ 4.3
+ 3.9
28.0 r 7.4
I.
7.1
6.4
3.9
3.1
5.2
2.5
Water
- -._---
l.l_
-~
It 4.9
t 3.3
f 4.1
t 3.9*
r 3.0
L 3.2
34.0 i 8.3
7.3
9.4
3.4
6.2
6.2
3.2
A bafado
---
i.p.
i.p.
i.p.
0.9 t
1.7
2.1 ?: 2.0
0.7 t
1.8
13.4 f 18.2
0.8 r
1.3
1.1 c
1.8
311.2 F 182*
lh
Catatonia (s 2 SD.)
2.1 +
5.3
1.9 f
2.1
1.2 +
1.6
23.8 + 31.4
4.7 f
5.3
3.2 f
4.6
893.0 ? 192%
2h
0
0
0
0
0
3
lh
0
0
0
0
0
4*
2h
Ptosis (median)
I FROM
*Differs significantly from control and abafad~ I groups f*P < 0.02; Duncans new multiple range test for catatonia and Kruska!Wallis analysis of variance followed by Mann-Whitney U-test for ptosis).
4 ml/kg
20 mglkg
100 mg/kg
Water
Citral
Citral
oral
oral
oral
oral
8 d/kg
c 10
c
1 r&/kg
Water
Route
Dose
Abafado I
Abafado I
Haloperidol
Material or
preparation
MEASUREMENT OF CATATONIC REACTION AND PALPEBRAL PTGSIS OF RATS TREATED WITH ABAFADO
L~MONGRASS OF SP;O PAUL0 OR WITH CITRAL
TABLE 8
__
55
leaves from
tonic conwas also
In contrast,
Pe~tylenetetrazol-induced convulsions
As seen in Table 11, oral doses C5,, of abafado I from fresh or dried leaves
from Sbo Paulo, as well as 50-100
mg/kg of citral, given by oral or i.p.
routes, did not give the mice protection
against the effects of pentylenetetrazol.
Neophobia reaction
The rats treated orally with 8.0 ml/kg of water, as expected, took 60 min
to begin to ingest the novel food available to them (Table 12). At that time
4 of the animals treated with the anxiolytic drug diazepam had already ingested the food, one of them starting the ingestion at 30 min. At 90 min the
diazepam group also ate significantly more than controls.
The rats treated with dose CZo of the abafudo did not eat at all during the
entire 90-min period.
swished response test
As seen in Table 13, the three groups of rats, in the last control session
emitted a small number of punished responses (licks during the sound period
signalizing the electrical shocks). The performances
during the experimental
session revealed that the vehicle and the abafudos I and III did not interfere
with the behavior of the rats. However, as expected, diazepam significantly
increased the number of punished responses by the rats.
Discussion
The folk use of lemongrass to treat feverish conditions (Alves et al., 1960;
Fook, 1980; Olaniyi et al., 1975) was the first of three popular therapeutic
indications on which we focused in the present work. As seen in Table 1,
doses CzO and ChOof abafudos obtained from the plants harvested in Sao
Paul0 and Ceara States were not able to significantly decrease body temperature of rats, when administered by the oral route. Citral, by the oral route, up
oral
oral
oral
i.p.
oral
i.p.
Route
1.6
1.9
1.6
1.4
tr 0.2
r. 0.5
r 0.3
t 0.6
-
Latent y
(min t S.D.)
Stereotyped
OF L~MONGRASS
IN RATS
behavior
r 4.0
2 6.4
* 6.2
* 7.9
r 0.3*
0*
5.0
4.5
4.0
6.0
0*
0
ON THE STEREO-
Grade
(median)
AND OF CITRAL
55.7
58.5
52.6
62.3
0.5
Total time
(min t S.D.)
OF SAO PAUL0
8 ml/kg
C 10
c
l;;o mg/kg
1 mg/kg
1 mg/kg
Water
Abafado I
Abafado I
Citral
Haloperidol
Haloperidol
*Differs significantly
analysis of variance
Dose
per dose.
Material
or preparation
Eight animals
TABLE 9
10
Water
Abafado I
Abafado II
Citral
Citral
Citral
Diphenylhvdantoin
Water
Abafado I
Abafado II
Material or
preparation
Cearl
Cearl
-
40 ml/kg
C 50
C 100
100 mg/kg
50 mg/kg
100 mg/kg
5 mglkg
2.0 ml/kg
C 5(1
C 50
SHo Paul0
Sio Paul0
Dose
Source
oral
i.p.
i.p.
oral
oraf
oral
oral
oral
Route
100
100
80
90
100
100
0
100
100
90
Tonic
convulsions
w1
30
30
20
30
20
20
0
20
10
10
Deaths
(at
TABLE
20 ml/kg
C 50
C 50
100ml/kg
20
mg/kg
50 mg/kg
100 mglkg
Water
Fresh leaves
Dried leaves
Citral
Water
Citral
Citral
oral
i.p.
i.p.
i.p.
oral
oral
oral
Route
100
100
100
100
100
100
Clonic
convulsions
(%)
0
0
0
8 ml/kg
C
5 *&g/kg
Water
Abafado I
Diazepam
0
0
0.06
30 min
0.13 f: 0.26
0
0.89 t 0.42*
60 min
(g t S.D.) after
;::
100
100
100
90
100
Deaths
(%)
0.24 * 0.18
0
0.91 + 0.13*
90 min
90
100
100
100
90
100
Tonic
convulsions
(%)
*Differs significantly from controls (P g 0.05; one-way analysis of variance followed by the Students f-test).
15 min
Food consumption
Dose
Material
or
preparation
The drugs were administered through oral route. Six animals per dose.
TABLE 12
Dose
Material
or
preparation
EFFECT OF ABAFADQ I FROM LEAVES OF LEMONGRASS OF SAG PAUL0 AND OF CITRAL ON THE CONVULSIONS
AND DEATHS PRODUCED IN MICE BY 100 mg/kg PENTYLENETETRAZOL
SC.
TABLE 11
59
TABLE 13
EFFECT OF ABAFADOS
I AND III FROM DRIED LEAVES OF LEMONGRASS OF
SK0 PAUL0 ON THE NUMBER OF PUNISHED RESPONSES EMITTED BY PREVIOUSLY TRAINED RATS (PUNISHED LICKING TEST)
Six animals per dose.
Material
or
preparation
Dose
_-Water
Abafado I
Abafado III
Diazepam
8 ml/kg
C 20
C
3 &g/kg
Experimental
session
2.7 ?: 0.5
3.2 * 2.4
-
5.7
2.0
2.7
13.0
4.5 r 1.6
_-
i
r
t
r
2.0
0.7
0.9
2.3*>1
to 200 mg/kg, also lacked effect. However, when the abafado or citral was
injected intrape~toneally si~ific~t
decreases of about 2C were obtained.
The lack of effect by oral route was also observed when a dose CZoof the
abafado was given to rats made hyperthermic by previous administration of
a pyrogen. The non-effectiveness of oral doses of lemongrass contrasts with
the positive results found with other Brazilian plants. Thus, oral doses of
2.5 and 5.0 ml/kg of an abafudo from seeds of Licaria puchury-major
(prepared by pouring 100 ml of boiling water over 5 g of powdered seeds)
signific~tly reduced the temperature of rats (Carlini et al., 1983).
The treatment of gastrointestinal disturbances is another folk medicinal
use of oral preparations of lemongrass (Alves et al., 1960; Fook, 1980;
Hirschhorn, 1983; LiberaIli et al., 1946; Olaniyi et al., 1975). Defecation of
rats in an open-field arena and intestinal transit in mice were the methods we
employed to investigate this attributed effect of the plant. The results
obtained were negative. As seen in Table 2, the abafudo I from S&o Paul0
and Ceari States was not able to decrease the intestinal transit of mice up to
the dose Cloo by oral route; 200 mg/kg of citral orally also was inactive.
Again, these compounds demonstrated activity by i.p. route. Similar results
were obtained with rats defecation scores in an open-field arena, as shown in
Table 3. Doses CZOof abafado I orally or C,,, intraperitoneally slightly
decreased defecation but the results fell short of statistical significance; only
100 mg/kg of citral i.p. significantly decreased defecation.
At least in Brazil, the main popular use of lemongrass is to treat nervous
disturbances such as insomnia, anxiety, tension and irritabilty, etc. It is
60
61
62
63
Kokate,
C.K., Rao, R.E. and Varma, K.C. (1971)
Pharmacological
investigation
of
essential oil of Cymbopogon
nardus (L.) Rendle:
studies on central nervous system.
Biological Abstracts
54, 973 (Abstract
10065).
Krall, R.L., Penry, J.K., White, B.G., Kupferberg,
H.J. and Swinyard,
E.A. (1978)
Antiepileptic
drug development.
II. Anticonvulsant
drug screening.
Epilepsia 19, 409-428.
Liberalli,
C.H., Helou, J.H. and Franca, A.A. (1946)
Contribui$o
ao estudo das gramineas aromaticas.
0 campim-limao
- Cym bopogon citratus (DC.) Stapf. Retjista Braslleira de Farmacia
Abril 1946, 189-209.
Masur, J. (1972)
Sex differences
in emotionality
and behavior of rats in the open-field.
Behavioral Biology 7, 749-754.
Matos, F.J.A.,
Riedel,
O.O., Queiroz,
M.F.F.B.
and Cavalcante,
F.S. (1982)
Plantas
Medicinais
de uso popular no Cearl. Proceedings
do VII Simposio
de Plantas Medicinais do Brasil, Belo Horizonte,
p. 119.
Matos, F.J.A.,
Alencar, J.W., Craveiro, A.A. and Fonteles,
M.C. (1984)
Distin$o
quimica
e farmacologica
de clones de Cymbopogon
citratus cultivados
no CearL e em SZo
Paulo. Ciencia e Cultura 36, 546.
Monti, J.M. and Carlini, E.A. (1975)
Spontaneous
behavior and sleep-wakefulness
cycle in
isolated and paired REM sleep deprived-marihuana
treated rats. Pharmacology,
Biochemistry
and Behavior
3,1025-1030.
Nogueira,
M.J.C. (1983)
Fitoterapia
popular e enfermagem
comunitaria.
Tese de livreDocencia
apresentada
ao Departamento
de Enfermagem
Medico-Cirdrgica
da Universidade de S;ib Paulo.
Olaniyi, A.A., Sofowora,
E.A. and Oguntimehin,
B.O. (1975)
Phytochemical
investigation
of some Nigerian plants used against fevers. II. Cymbopogon
citrafus. Planta Medica
28,186-189.
Oliveros-Belardo,
L. and Aureus, E. (1980)
Essential
oil from Cymbopogon
citratus (DC.)
Stapf growing wild in the Phillipines.
Chemical Abstracts
92, 425 (Abstract
371688).
Paviani, T.I. (1964)
Algumas considera@es
acerca da anatomia
foliar do Cymbopogon
citratus (DC.) Stapf. Revista da Faculdade
de Farmacia de Santa Maria 10, 97-108.
Peigen, X. (1983)
Recent developments
on medicinal
plants in China. Journal of Ethnopharmacology
7, 95-109.
Poschel,
B.P.H. (1971)
A simple and specific screen for benzodiazepine-like
drugs.
Psychopharmacologia
(Berl.),
19, 193-198.
Rabha, L.C. Baruah, A.K.S. and Bordoloi,
D.N. (1980)
Search for aroma chemicals
of
commercial
value from plant resources
of North East India. Chemical
Abstracts
93, 504 (Abstract
79858n).
Radwan,
A.S. (1975)
An analytical
method
for proximadiol,
the active principle
of
Cymbopogon
proximus.
Planta Medica 27, 93-97.
Reily,
H. and Spinks,
A. (1958)
Biological
assessment
of tranquilizers.
Journal
of
Pharmacy
and Pharmacology
10,657-671.
Sell, A.B. and Carlini, E.A. (1976)
Anesthetic
action of methyleugenol
and other eugenol
derivatives.
Pharmacology
14, 367-377.
Seto, T.A. and Keup, W. (1969)
Effects of alkylmethoxybenzene
and alkylmethylenedioxibenzene
essential
oils on pentobarbital
and ethanol sleeping-times.
Archives
Internationales
de Pharmacodynamie
et de Thkrapie 180, 232-240.
Silva, G.A.A. and Bauer, L. (1971)
0 oleo essential
de Cymbopogon
citratus no Rio
Grande do Sul. Revista Brasileira de Farmcicia 52, 193-196.
Silveira Filho, N.G. and Tufik, S. (1981)
Comparative
effects between cannabidiol
and
diazepam on neophobia,
food intake and conflict
behavior. Research
Communications
in Psychology,
Psychiatry
and Behavior 6, 251-266.
Sylva da, M.G. (1960)
Lemon-grass
oil from Ceylon.
Chemical
Abstracts
54, 4002d.
Swinyard,
E.A., Brown, W.C. and Goodman,
L.S. (1952)
Comparative
assays of antiepileptic drugs in mice and rats. Journal of Pharmacology
and Experimental
Therapeutics
106,319-330.
64
Troncone,
L.R.P., Ferreira, T.M.S., Braz, S., Silveira-Filho,
REM sleep deprivation
supersensitivity
and its reversion
Research
Communications
citratus
Garcia