Screening
of Plants Constituents for effect on Glucose Transport Activity
in Ehrlich Masticates Tumour Cells
Sadahiko Ishibashi, Fabian Dayrit, William
G. Padolina, and Kazuo Yamasaki. Chikage, Murakami, Keiko
Myoga, Ryoji Kasai, Kazuhiro Ohttani, Tomonori Kurokawa
Institute of Pharmaceutical Sciences, Hiroshima University
School of Medicine, 1-2-3 Kasumi, Minami-Ku, Hiroshima, Japan
Depar™ent of Chemistry. Received May 10, 1993
The effect of plant extracts on D-glucose uptake by Ehrlich
ascot tumour cells was examined. Among the 23 extracts of
medicinal plants, five samples inhibited, and six samples
activate, the uptake significantly. From one of the active
plants, Lagerstroemia specious, two tritepenoids, colosolic
acid and maslinic acid were isolated. Colosolic acid was shown
to be a glucose transport activator. Since the compound was
known to have hypoglycemic activity, our simple in vitro bioassay
method can at least be used for anti-diabetic activity
Glucose transport is one of the most important functions of
all cells to acquire energy. Several types of a glucose transporter
are known in cell membranes of mammalian tissues. Glucose
transporter is important in regulating the level of intracellular
glucose.
Modification of the activity of glucose transport would cause
several physiological effects, i.e., lowering blood glucose
level, etc. Up to now, only a few compounds have been known
to affect glucose transport activity. The compounds, which
inhibit glucose transporter activity, are forskolin, diterpene
isolated from Labiatac plant, phorezin, and dihydrochalcone
of Rosaceae and cylochalasm B, one of the mycoloxins. On the
other hand, no other agent able to increase glucose transport
activity is known except insulin, a pancreatic hormone, which
regulates sugar increasingly.
Systematic research in the pursuit of an agent to modify glucose
transport actively has been carried out in search for a new
type of agent for the trea™ent of diabetes, a tonic for the
aged, etc. In particular, finding of activator is more important.
In this report we describe the establishment of a screening
method for measuring glucose transport activity which can
be used for rapidly evaluating many types of sample, ranging
from crude extracts to pure compounds.
Ehrlich ascites tumour cells were used to measure glucose
transport activity because this cell are known to contain
a glucose transporter, and they can be easily propagated and
used as an experimental system without the need for a complex
procedure to separate cells, which might injure the cellular
membrane.
The finding of a glucose transport activator in plant extracts
and the isolation of an active principle from one of these
active plant extracts are also described.
Result
and Discussion
The time course of 2-deoxy-D-glucose (2DG)
uptake by Ehrlich cells was measured (Fig.1). The rate of
uptake was linear up to 2 min at concentration of 0.2 –
1 mM. Accordingly, experiments with test solutions were carried
out using an incubation time of 1min. Under these experimental
conditions, the Km and Vmax values were 1.7 mM and 1.4 mnol/min/10^6
cells, respectively, calculated from Lineweaver- Bark plots.
The Km value obtained was consistent with reported value with
reported value for type 1 glucose transporter.
The effect on glucose transport activity of forskolin, a known
glucose transport inhibitor, was measured in this system,
it inhibited 2-DG uptake at a concentration of 20mm by 51%
(Fig. 2). Forskolin can accordingly be used as control in
our system.
Then the effect of 23 methanolic extracts of medicinal plants
on glucose transport activity was measured at three different
concentrations. The plants were randomly chosen from Southeast
Asia herbal medicine (Table 1), and Japanese medicinal plants
used mainly for the trea™ent of diabetes (Table II). Among
the 23 samples, 6 samples accelerated 2-DG uptake and 5 reduced
it, while the others were ineffective. (Fig. 3)
Although both effects were interesting, we focused on stimulation
in this report. Since, as mentioned above, no stimulating
agent of glucose transport has been reported except insulin.
In addition, among the plants exhibiting a positive effect,
Lagerstroemia speciosa and Alomordica charantia were used
as antidiabetic agents in the Southeast Asia, and the hypoglycemic
effect of Tinospora cordifolia (syn. T. namphii) has recently
been reported. Preliminary results of the effect of ginseng
extract have also been reported. These screening results prompted
us to study the active principle of this glucose transport
stimulating plants.
The target plant, Lagerstroemia speciosa L. is distributed
all over the Southeast Asia, as well in India, South China
and tropical Australia. The leaves of this plant are called
"Banaba" in the Philippines, and used as an anti
diabetic, the decoction has been clinically tested and found
to reduce blood sugar.
The bioactive McO11 extract of banaba was fractionated and
subjected to column chromatography. The bioactivity of each
fraction was monitored at each stage of the isolation process.
From the active McO11 fraction eluded from a Diaion HP-20
chromatography column, compounds 1 and 2 were isolated by
silica-gel column chromatography in yields of 0.01 and 0.0016%,
respectively. Compounds 1 and 2 were identified by means of
NMR as known tritepenes, colosolic acid (2a-hydroxyursoloic
acid) and maslinic acid (2a-hydroxyoleanolic acid), respectively.
The bioactivity of 1 and 2 was measured by the above method.
Colosolic acid (1) showed a significant glucose transport-stimulating
activity at a concentration of 1mm, while 2 were inactive
(Table III).
The hypoglycemic effect of 1 has recently been reported in
normoglycemic rats following oral administration. This evidence
strongly suggest that our in vitro bioassay is closely related
to the hypoglycemmic effect and maybe used as a first screening
method for anti-diabetic substances without the need for any
animals, as in an in vivo assay. Examinations of the correlation
of both activities and a further search for active substances
in other plants are in progress.
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