Benzophenone C - And O -glucosides from Cyclopia genistoides (Honeybush) inhibit mammalian α-glucosidase

Article abstract of DOI:10.1021/np5007247

An enriched fraction of an aqueous extract prepared from the aerial parts of Cyclopia genistoides Vent. yielded a new benzophenone di-C,O-glucoside, 3-C-β-d-glucopyranosyl-4-O-β-d-glucopyranosyliriflophenone (1), together with small quantities of a known benzophenone C-glucoside, 3-C-β-d-glucopyranosylmaclurin (2). The isolated compounds showed α-glucosidase inhibitory activity against an enzyme mixture extracted from rat intestinal acetone powder. Compound 2 exhibited significantly (p < 0.05) higher inhibitory activity (54%) than 1 (43%) at 200 μM. In vitro tests in several cell models showed that 1 and its 3-C-monoglucosylated derivative (3-C-β-d-glucopyranosyliriflophenone) were marginally effective (p ≥ 0.05) in increasing glucose uptake.

Full text of DOI:10.1021/np5007247

Article
pubs.acs.org/jnp
Benzophenone C- and O‑Glucosides from Cyclopia genistoides
Honeybush) Inhibit Mammalian α‑Glucosidase
(
,
†,‡
§
‡
‡
Theresa Beelders,* D. Jacobus Brand, Dalene de Beer, Christiaan J. Malherbe,
Sithandiwe E. Mazibuko, Christo J. F. Muller, and Elizabeth Joubert
⊥
⊥
†,‡
†
Department of Food Science, Stellenbosch University, Private Bag X1, Matieland 7602, South Africa
‡
Post-Harvest and Wine Technology Division, Agricultural Research Council (ARC) Infruitec-Nietvoorbij, Private Bag X5026,
Stellenbosch 7599, South Africa
§
Central Analytical Facility (CAF), Nuclear Magnetic Resonance Unit, Private Bag X1, Matieland 7602, South Africa
⊥
Diabetes Discovery Platform, South African Medical Research Council, P.O. Box 19070, Tygerberg 7505, South Africa
S Supporting Information
*
ABSTRACT: An enriched fraction of an aqueous extract prepared from the aerial parts of Cyclopia genistoides Vent. yielded a
new benzophenone di-C,O-glucoside, 3-C-β-D-glucopyranosyl-4-O-β-D-glucopyranosyliriflophenone (1), together with small
quantities of a known benzophenone C-glucoside, 3-C-β-D-glucopyranosylmaclurin (2). The isolated compounds showed α-
glucosidase inhibitory activity against an enzyme mixture extracted from rat intestinal acetone powder. Compound 2 exhibited
significantly (p < 0.05) higher inhibitory activity (54%) than 1 (43%) at 200 μM. In vitro tests in several cell models showed that
1
and its 3-C-monoglucosylated derivative (3-C-β-D-glucopyranosyliriflophenone) were marginally effective (p ≥ 0.05) in
increasing glucose uptake.
he global prevalence of diabetes is increasing at alarming
Recent investigation of the phenolic constituents of C.
genistoides revealed the presence of several benzophenone C-
T
rates, leading to estimates of 439 million diabetics by
1
2
030. In Africa, South Africa tips the scale with a national
glucosides, including 3-C-β-D-glucopyranosyliriflophenone and
2
14−16
prevalence of over 7%. It is projected that diabetes will rank as
the ninth leading cause of death in low-income countries in the
3-C-β-D-glucopyranosylmaclurin.
The major benzophe-
none glycoside present in hot water extracts of C. genistoides
has been tentatively identified as an iriflophenone di-O,C-
3
next few decades. A sedentary lifestyle together with an
16
unhealthy diet, high in refined carbohydrates accompanied by a
low intake of fruits and vegetables, are considered contributing
factors. The search for natural and synthetic α-glucosidase
hexoside thus far. A compound with similar MS properties
has also been observed in extracts of another Cyclopia species,
17
C. subternata, albeit at lower concentrations. In the present
paper the isolation and structural elucidation of this
benzophenone glucoside, identified as 3-C-β-D-glucopyrano-
syl-4-O-β-D-glucopyranosyliriflophenone (1), is described.
During the isolation process, small quantities of the known
benzophenone C-glucoside 3-C-β-D-glucopyranosylmaclurin
4
,5
inhibitors
that delay the breakdown and absorption of
carbohydrates in the gut, thus mimicking the protective effect of
6
the drug acarbose, but without its side-effects, is escalating.
Much prominence is given to polyphenols, with promising
4
results in vitro. Synergistic effects between acarbose and
(
2) was also obtained. These compounds were isolated from
the aerial parts of C. genistoides using solid-phase extraction
SPE) for extract enrichment, followed by purification by
polyphenols suggest benefits in terms of dose reduction of the
7
drug. Subclasses of phenolic compounds that show promise as
(
α-glucosidase inhibitors include the polyhydroxyxanthones and
semipreparative liquid chromatography (LC). The ability of 1
and 2 to inhibit mammalian α-glucosidase was assessed and
polyhydroxybenzophenones, together with their glycosylated
8
−11
derivatives.
Extracts of Cyclopia genistoides Vent. (honey-
bush) are principally renowned for high levels of the
1
2
tetrahydroxyxanthone C-glucoside mangiferin, a bioactive9
Received: September 16, 2014
1
3
compound with potent α-glucosidase inhibitory activity.
©
XXXX American Chemical Society and
American Society of Pharmacognosy
A
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Journal of Natural Products
Article
compared to that of 3-C-β-D-glucopyranosyliriflophenone.
Included in the α-glucosidase assay was the benzophenone
aglucone maclurin, with acarbose employed as positive control.
To date, the α-glucosidase inhibitory activities of 1 and 2 as C-
and O-glucosylated polyhydroxybenzophenones have not been
assessed. In vitro tests in several cell models were conducted to
investigate the ability of 1 and 3-C-β-D-glucopyranosyliriflo-
phenone to increase glucose uptake in vitro.
anosyl moieties at δ 4.73 (1H, d, J = 7.8 Hz) and 4.66 (1H, d, J
= 9.8 Hz) were irradiated selectively utilizing a 1D NOESY
experiment to determine their position of attachment and other
proton resonances of the individual O- and C-linked
glucopyranosyl units. The anomeric proton of the glucopyr-
anosyl residue at δ 4.73 (1H, d, J = 7.8 Hz, H-1‴) displayed a
strong NOE association with the H-5 singlet at δ 6.24. This
assigned the O-linked glucosyl unit to C-4 of the
benzophenone A-ring. A weak NOE association of H-1‴ with
H-4″ (δ 3.24) of the neighboring glucosyl moiety indicated the
close proximity of the glucosyl entities.
An NOE association was also observed between the three
axial H-1‴, H-3‴, and H-5‴ protons (Figure 1), affirming the
RESULTS AND DISCUSSION
Compound 1 was obtained as a white, amorphous powder. Its
■
Figure 1. Relevant NOE associations in 1.
molecular formula was established as C H O from the
2
5
30 15
1
3
analyses of its HRESIMS and C NMR data. Initial LC-
glucose configuration of the O-linked sugar unit. The nature of
the C-linked sugar to the aglycone was confirmed by
comparison of the hydrolytic products to the NMR spectra
of the commercial 3-C-β-D-glucopyranosyliriflophenone stand-
ard.
A COSY experiment confirmed the AA′BB′ aromatic spin
system of the B-ring and the connectivity of some of the
protons on the individual glucosyl moieties. This includes only
the protons that are sufficiently resolved to be assigned by the
COSY experiment and did not overlap with the glucosyl proton
resonances.
ESIMSMS analyses of this compound in a C. genistoides sample
1
6
matrix had pointed to an iriflophenone di-O,C-hexoside. The
elucidation of the structure of 1 and, in particular, the
identification of the hexoside moieties and their point of
attachment to the aglycone, were done via 1D and 2D NMR
experiments. The relative configurations of the glycoside units
can normally be determined by a 1D/2D NOESY NMR
experiment. However, NMR spectroscopic data for 1 proved
inconclusive for unambiguous identification of the individual
glycoside units, due to overlapping proton resonances. Since
the NMR spectra of 1 closely resembled those of 3-C-β-D-
glucopyranosyliriflophenone, it was essential to first selectively
hydrolyze and identify the terminal O-linked sugar moiety,
followed by comparison of the resulting iriflophenone C-
hexoside to that of a commercial 3-C-β-D-glucopyranosyl-
The HSQC NMR experiment was used to assign all the
1
directly bonded protons ( JHC) to their respective carbons. All
the carbons were resolved successfully by an HMBC experi-
2
3
ment showing the long-range ( J , J ) connectivity between
HC
HC
18
4
protons and carbons [up to four bonds ( JHC) in some cases].
Those structurally significant HMBC correlations are shown in
Figure 2, enabling the assignment of the unprotonated carbons
in the molecule. Compound 1 was thus identified as 3-C-β-D-
glucopyranosyl-4-O-β-D-glucopyranosyliriflophenone.
iriflophenone standard, also present in C. genistoides.
The terminal O-linked hexoside moiety was identified as D-
glucose by enzymatic hydrolysis and GC-MS analysis. The
1
resulting iriflophenone C-hexoside was purified, and its H and
1
3
C NMR data matched those of 3-C-β-D-glucopyranosyl-
Compound 2 was obtained as a light yellow, amorphous
powder. Accurate measurement of the pseudomolecular ions in
the positive and negative HRESIMS data, in conjunction with
iriflophenone. Having identified the β-D-glucopyranosyl con-
stituent units, the rest of the molecule and the point of
attachment of the O-β-D-glucopyranosyl unit were defined by
additional 1D NOESY, COSY, HSQC, and HMBC NMR
experiments.
13
C NMR data, allowed a molecular formula of C H O to be
19 20 11
assigned to 2. The structure of 2 was confirmed as 3-C-β-D-
1
The aromatic region between 6.0 and 8.5 ppm of the H
NMR spectra showed two o-coupled doublets and a singlet, δ
7
.61 (2H, d, J = 8.6 Hz), 6.78 (2H, d, J = 8.6 Hz), 6.24 (1H, s),
reminiscent of an AA′BB′ aromatic spin system with an
uncoupled singlet on a separate aromatic ring and supported by
1
3
the presence of aromatic carbons in the C NMR spectra of 1.
The H NMR spectra also presented the resonances of two β-
1
coupled (∼8 Hz anomeric coupling constant) glucoside units in
19
the characteristic 2.5−5.0 ppm region. The presence of a
single carbon at δ 193.1 in addition to the 12 aromatic carbons
13
in the C NMR spectrum was reminiscent of a benzophenone
aglycone unit. The anomeric protons of the two glucopyr-
1
9
Figure 2. Relevant long-range HMBC correlations in 1.
B
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glucopyranosylmaclurin by comparison of its observed and
reported H NMR and C NMR spectroscopic data.
iriflophenone (ca. 27% increase; Figure 4B). Similar marginal
effects on glucose uptake were observed in 3T3-L1 adipocytes
(Figure 4C and D) and in C3A hepatocytes (data not shown).
It was anticipated that the isolated benzophenone glucoside (1)
and 3-C-β-D-glucopyranosyliriflophenone could increase in
vitro glucose uptake activity by activating the cellular energy
1
13
14,20
Both benzophenone derivatives 1 and 2, together with the
reference compounds, showed inhibitory activity against
mammalian α-glucosidase at various concentrations with all
values significantly differing (p < 0.05) from all other values.
The observed inhibitory activities were both concentration- and
compound-specific (Figure 3), showing a clear dose−response.
22,23
regulator AMPK, as demonstrated for the latter compound
y
in mature 3T3-L1 adipocytes and diabetic KK-A mice. The
assessed compounds were, however, less effective at increasing
cellular glucose uptake than the reference pharmacological
agent metformin, mechanistically known to be an activator of
24
AMPK.
EXPERIMENTAL SECTION
■
General Experimental Procedures. NMR spectra were recorded
1
on a Varian Unity Inova 600 NMR spectrometer with a H frequency
of 600 MHz and a 13C frequency of 150 MHz using a 5 mm inverse
detection PFG probe. The chemical shift frequencies are indicated on
1
13
the δ scale. H and C NMR spectra were referenced to the residual
DMSO-d peak at δ 2.5 and 39.5, respectively. The spectra in acetone-
6
1
d have the residual acetone peaks referenced at δ 2.05 for H NMR
6
13
and at δ 29.84 for the C NMR spectra. The spectra were recorded
using the standard VnmrJ instrument software and processed and
expanded further using the Mestrenova 9.0 software package.
HRESIMS analyses were conducted on an Acquity UPLC system,
fitted with a photodiode-array detector and coupled to a Synapt G2 Q-
TOF equipped with an electrospray ionization source (Waters,
Milford, MA, USA). UV spectra were recorded online. Chromato-
graphic conditions and MS parameters were as described by
Beelders. Semipreparative LC was performed on a LaChrom
HPLC system (Merck Hitachi, Hitachi High Technologies, Japan)
comprising a quaternary pump, autosampler, variable-wavelength
detector, and diode-array detector and fitted with a Phenomenex
Gemini C18 column (5 μm, 110 Å, 150 × 10 mm) (Phenomenex,
Torrance, CA, USA). The column was protected by a guard column of
the same stationary phase (10 × 10 mm) and a high-pressure
semipreparative in-line filter (IDEX Health & Science, Oak Harbor,
WA, USA). Column temperature was maintained at 30 °C using an
external HPLC column oven (LKB Bromma, Sweden). Gas
chromatography was performed on an Agilent GC-MS instrument
Figure 3. Percentage activity of rat α-glucosidase challenged with
various concentrations of 1, 3-C-β-D-glucopyranosyliriflophenone, 2,
and maclurin.
1
6
The activities of the benzophenones could thus be compared at
equimolar concentration levels, which gave insight into possible
structure−activity relations. Compound 2 was the most active
inhibitor, followed by 3-C-β-D-glucopyranosyliriflophenone and
1, while maclurin showed the weakest inhibitory activity. It
appears that C-monoglucosides tend to be more effective
inhibitors than their corresponding aglucones; that is, 2 is
significantly more active than maclurin (p < 0.05). This has also
been observed previously for 3-C-β-D-glucopyranosyl-
(
Agilent 6890N GC and Agilent 5975 MSD, Agilent Technologies,
Palo Alto, CA, USA) fitted with a 30 m Zebron ZB-SemiVolatiles
column with 0.25 mm inner diameter and 0.25 μm film thickness. The
GC chromatograms and mass spectra were evaluated using Agilent
MSD ChemStation (version D.02.00.237) software.
9
iriflophenone and its aglucone, iriflophenone. Furthermore,
the higher activity of 2 compared to that of 3-C-β-D-
glucopyranosyliriflophenone was attributed to the additional
Plant Material. The leaves and fine stems from a selection of
Cyclopia genistoides bushes (Overberg type) were harvested from a
commercial plantation situated near Pearly Beach (Western Cape,
South Africa; GPS coor. −34.702, 19.618). Plant material was dried
without delay in a cross-flow drying tunnel at 40 °C for 16 h to a
moisture content of less than 10% and pulverized using a Retsch rotary
mill (1.4 mm sieve; Retsch GmbH, Haan, Germany).
Extraction and Isolation. Plant material (420 g) was extracted
with hot water (4.2 L, 93 °C) for 30 min using a ratio of 1:10 (w/v).
The crude extract was filtered through Whatman #4 filter paper,
frozen, and freeze-dried using a VirTis Advantage Plus freeze-drier (SP
Scientific, Warminster, PA, USA). The freeze-dried hot water extract
(126.5 g) comprised 6.31% of 1 and 0.53% of 2.
Enrichment of the crude extract in terms of 1 and 2 was performed
using C18 solid-phase extraction (Discovery DSC-18; 10 g/60 mL;
Sigma-Aldrich). The cartridge was conditioned sequentially with
MeOH and deionized water (60 mL). A solution of freeze-dried
extract (300 mg reconstituted in 50 mL of deionized water) was
applied to the cartridge, followed by flushing with deionized water
3
′-hydroxy group of 2. Previous studies on hydroxybenzophe-
10 8
nones and hydroxyxanthones have shown that increases in
the number of phenolic hydroxy groups on the basic diphenyl
ketone and dibenzo-γ-pyrone structures lead to significant
increases in α-glucosidase inhibitory activities. Moreover, for
hydroxyflavones it has been shown that a 3′-hydroxy group in
21
particular leads to increased inhibitory activity. The presence
of an additional O-glucopyranosyl moiety at C-4 on the
diphenyl ketone structure of 1 significantly (p < 0.05) lowered
α-glucosidase inhibitory activity compared to 3-C-β-D-
glucopyranosyliriflophenone. A similar decrease in activity
due to an additional C-glucopyranosyl moiety has also been
reported for 3-C-β-D-glucopyranosyl-5-C-β-D-glucopyranosyl-
iriflophenone compared to 3-C-β-D-glucopyranosyl-
9
iriflophenone.
The effect of 1 and 3-C-β-D-glucopyranosyliriflophenone on
in vitro glucose uptake in L6 myocytes demonstrated marginal,
but not significant, increases in glucose uptake relative to the
vehicle control at concentrations of 10 μM of 1 (ca. 22%
increase; Figure 4A) and 100 μM of 3-C-β-D-glucopyranosyl-
(
100 mL). The target analytes were eluted with 5% aqueous MeOH
(300 mL). This process was repeated 48 times with new cartridges
(14.4 g of freeze-dried extract loaded), and the eluants were pooled,
vacuum-evaporated, and freeze-dried, yielding ca. 1.2 g of enriched
C
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Journal of Natural Products
Article
3
Figure 4. H-2-DOG uptake in L6 myocytes exposed to (A) 1 and (B) 3-C-β-D-glucopyranosyliriflophenone and 3T3-L1 adipocytes exposed to (C)
1
and (D) 3-C-β-D-glucopyranosyliriflophenone. Insulin (positive control) and metformin (reference drug control) were included at concentrations
of 1 μM. Mean activity is expressed relative to the vehicle control at 100% ± standard error of the means. Three independent experiments were
performed each with three technical repeats. **p < 0.01; ***p < 0.001.
+
fraction. The enriched fraction comprised 56.5% of 1 and 4.8% of 2.
The average recovery of target analytes after SPE was 75%.
373 (10) [M + H − 162 − 2 × H O] , 355 (10) [M + H − 162 − 3 ×
2
2
+
+
+
H O] , 313 (10) [M + H − 258] , 289 (15) [M + H − 162 − 120] .
The enriched fraction was reconstituted in deionized water (ca. 6
mg/mL), filtered, and subjected to semipreparative LC (MeCN−2%
HOAc (aq), 4:96, v/v) using a flow rate of 4.8 mL/min. Aliquots (400
μL) of the reconstituted, enriched fraction were injected repeatedly,
equaling 880 mg. The fractions containing 1 and 2 were collected
based on retention times using a Gilson FC203B fraction collector
Acid Hydrolysis of 1. Aliquots of a solution of 1 (105 mg in 70
mL of 1.1 M HCl) were heated in 5 mL glass Reacti-vials at 60 °C in a
Stuart heating block (Bibby Scientific Limited, Stone, UK) for 24 h.
The hydrolysis reaction was monitored using HPLC-DAD (86%
degradation at t = 24 h). The hydrolyzed mixture was cooled to room
temperature and adjusted to pH ∼4 using 1.1 M NaHCO .
3
(
Gilson, Middleton, WI, USA) and pooled, and the organic solvent
One half of this hydrolyzed mixture was vacuum-evaporated and
subjected to semipreparative LC (MeCN−2% HOAc (aq), 8:92, v/v)
to obtain intact 1 and iriflophenone C-hexoside. The fraction
containing iriflophenone C-hexoside was collected based on retention
time, pooled, vacuum-evaporated, and freeze-dried, followed by NMR
was evaporated under vacuum. The remaining aqueous solutions were
filtered, frozen, and freeze-dried, yielding 370 mg of 1 (purity >99% by
HRESIMS; total yield of 74% from the enriched extract) and 30 mg of
2
(purity 95% by HRESIMS; total yield of 71% from the enriched
extract).
analysis.
3
-C-β-D -Glucopyranosyl-4-O-β-D -glucopyranosyl-
1H NMR and
13
C NMR Data for 3-C-β-D-glucopyranosyl-
iriflophenone (1): white, amorphous powder; UV λ online 234,
2
max
1
1
iriflophenone (hydrolyzed product of 1): H NMR 600 MHz
94 nm; H NMR 600 MHz (DMSO-d , 298 K) δ 7.61 (2H, d, J = 8.6
6
(
=
3
acetone-d , 298 K) δ 7.64 (2H, d, J = 8.6 Hz, H-2′, 6′), 6.85 (2H, d, J
6
Hz, H-2′,6′), 6.78 (2H, d, J = 8.6 Hz, H-3′,5′), 6.24 (1H, s, H-5), 4.73
8.6 Hz, H-3′, 5′), 5.99 (1H, s, H-5), 4.92 (1H, d, J = 9.8 Hz, H-1″),
(
1H, d, J = 7.8 Hz, H-1‴), 4.66 (1H, d, J = 9.8 Hz, H-1″), 3.6 (3H, m,
.85 (2H, d, J = 3.1 Hz, 2 × H-6″), 3.69 (H, t, J = 9.2 Hz, H-4″), 3.63
H-6″, 2 × H-6‴), 3.46 (2H, m, H-2″, H-6″), 3.25 (3H, m, H-3″, H-4″,
H-5″), 3.18 (2H, m, H-3‴, H-5‴), 3.08 (1H, t, J = 9.2 Hz, H-4‴), 2.88
(
H, t, J = 9.2 Hz, H-2″), 3.57 (H, t, J = 8.9 Hz, H-3″), 3.49 (H, m, H-
13
13
5″); C NMR 150 MHz (acetone-d , 298 K) δ 197.8 (CO), 162.6
(
1
1H, t, J = 8.4 Hz, H-2″); C NMR 150 MHz (DMSO-d , 298 K) δ
6
6
(
(
(
C-4′), 161.9 (C-4), 161.4 (C-2), 160.5 (C-6), 133.3 (C-1″), 132.5
C-2′, 6′), 115.3 (C-3′, 5′), 106.6 (C-1), 104.7 (C-3), 96.9 (C-5), 82.1
C-5″), 79.3 (C-3″), 76.6 (C-1″), 74.6 (C-4″), 70.6 (C-2″), 61.7 (C-
93.1 (C, CO), 161.8 (C, C-1′), 157.7 (C, C-1), 155.2 (C, C-2),
1
55.2 (C, C-4), 131.8 (CH, C-3′, 5′), 130.2 (CH, C-4′), 114.8 (CH,
C-2′, 6′), 110.0 (C, C-6), 106.2 (C, C-3), 100.5 (CH, C-1‴), 94.8
(
CH, C-5), 81.0 (CH, C-3″), 78.0 (CH, C-5″), 77.1 (CH, C-5‴), 76.6
6″).
(
CH, C-3‴), 74.9 (CH, C-1″), 73.2 (CH, C-2‴), 72.3 (CH, C-2″),
Identification of the O-Linked Hexose Residue in the
Hydrolyzed Product. The other half of the hydrolyzed product
was partially evaporated under vacuum, and a small volume of the
concentrated liquid was removed for an enzyme robot assay. This
assay was conducted on a Thermo Scientific Arena 20XT random
access chemistry analyzer (Thermo Fisher Scientific, Oy, Finland) with
the use of an Enytec fluid D-glucose no. 5140 enzyme reagent kit
6
6
5
9.3 (CH, C-4″), 69.3 (CH, C-4‴), 60.5 (CH C-6‴), 60.1 (CH , C-
2
,
2
−
″); HRESIMS m/z 569.1503 [M − H] (calcd for C H O ,
96.1506); ESIMS [m/z (%)] 569 (100) [M − H] , 1139 (20) [2M −
2
5
29 15
−
−
+
H] ; HRESIMS m/z 571.1661 [M + H] (calcd for C H O ,
5
H] , 409 (100) [M + H − 162] , 391 (60) [M + H − 162 − H O] ,
25
31 15
+
71.1663); ESIMS [m/z (%)] 1141 (10) [2M + H] , 571 (60) [M +
+
+
+
2
D
dx.doi.org/10.1021/np5007247 | J. Nat. Prod. XXXX, XXX, XXX−XXX

Journal of Natural Products
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(
AEC-Amersham, Kayalami, South Africa) for the identification of
°C for 15 min, followed by the addition of 40 μL of the substrate, 1.2
mM 7-O-α-D-glucopyranosyl-4-methylumbelliferone, by dispenser.
glucose according to the manufacturer’s instructions.
The remaining sample volume was freeze-dried, derivatized with
bis(trimethylsilyl)trifluoroacetamide (BSTFA) using the procedure
described by Roessner, and subjected to GC-MS analysis. D-Glucose
and D-galactose standards (Sigma-Aldrich) were also derivatized prior
to analysis. Sample volumes of 1 μL were injected with a split ratio of
Fluorescence (λ : 360 nm; λEM: 460 nm) was monitored over 30
min, and the net fluorescence (net FL) and percent enzyme activity
were calculated using the following formulas:
EX
25
Net FL = Fluorescence30min − Fluorescence0min
1
:10. The injection temperature was 280 °C, the interface set to 280
°C, and the ion source adjusted to 240 °C. The carrier gas was helium
Net FL
set at a constant flow rate of 1.0 mL/min. The temperature program
comprised a 6 °C oven temperature ramp from 70 to 76 °C within 1
min, followed by a 32 °C/min ramp to 300 °C, and a final 5 min
heating at 300 °C. Mass spectra were recorded over an m/z scanning
range of 40 to 650. Electron energy was 70 eV and solvent delay 8 min.
sample
%
Enzyme Activity = 100 × Net FL
assay control
Statistical analysis was performed with GraphPad Prism version 5.00
for Windows (GraphPad Software, San Diego, CA, USA, www.
graphpad.com) using one-way ANOVA with Tukey’s multiple
comparison posthoc test to determine significant differences between
values at the 95% confidence level (p < 0.05).
3
-C-β-D-Glucopyranosylmaclurin (2): light yellow, amorphous
1
powder; UV λmax online 236, 290 (sh), 318 nm; H NMR 600 MHz
DMSO-d , 298 K) δ 7.15 (1H, d, J = 1.93 Hz, H-2′), 7.06 (1H, dd, J
(
=
5
(
6
1.93, 8.24 Hz, H-6′), 6.74 (1H, d, J = 8.24 Hz, H-5′), 5.94 (1H, s, H-
3
3
2
-Deoxy-[ H]-D-glucose ( H-2-DOG) Uptake. To estimate in
), 4.60 (1H, d, J = 9.77 Hz, H-1″), 3.61 (1H, d, 10.96 Hz, H-6a), 3.51
3
13
vitro glucose uptake activity, cellular H-2-DOG uptake was assessed
2H, m, H-2″, 6″), 3.20 (3H, H-3″, 4″, 5″); C NMR 150 MHz
by liquid scintillation counting, using the method described by
(
DMSO-d , 298 K) δ 194.6 (C, CO), 158.4 (C, C-4), 156.7 (C, C-
6
2
7
4
Mazibuko. Briefly, L6 myoblasts (2.5 × 10 cells/mL) and 3T3-L1
6
1
3
3
), 156.3 (C, C-2), 150.0 (C, C-4′), 144.6 (C, C-3′), 131.0 (C, C-1′),
22.3 (CH, C-6′), 116.2 (CH, C-2′), 114.7 (CH, C-5′), 107.6 (C, C-
), 103.6 (C, C-1), 94.8 (CH, C-5), 81.1 (CH, C-5″), 78.3 (CH, C-
4
fibroblasts (2.0 × 10 cells/mL) were seeded into 24-well plates in
Dulbecco’s modified Eagle’s medium (DMEM) supplemented with
″), 74.8 (CH, C-1″), 72.1 (CH, C-4″), 69.6 (CH, C-2″), 60.4 (CH ,
10% fetal or normal calf serum, respectively. C3A hepatocytes were
2
−
4
C-6″); HRESIMS m/z 423.0933 [M − H] (calcd for C H O ,
seeded at 5.5 × 10 cells/mL in Eagle’s minimal essential medium
19
19 11
−
4
23.0927); ESIMS [m/z (%)] 1271 (5) [3M − H] , 847 (70) [2M −
(EMEM) supplemented with 10% fetal calf serum. All cells were
−
−
−
H] , 423 (100) [M − H] , 303 (20) [M − H − 120] ; HRESIMS m/
cultured at 37 °C in humidified air with 5% CO . Cell culture media
2
+
z 425.1075 [M + H] (calcd for C H O , 425.1084); ESIMS [m/z
DMEM, EMEM, and fetal and normal calf serum were obtained from
Lonza (Walkersville, MD, USA). The L6 myoblasts and 3T3-L1
fibroblasts were differentiated into myotubule-forming myocytes and
adipocytes, respectively, while the C3A hepatocytes were used as
19
21 11
+
+
(
%)] 425 (80) [M + H] , 407 (100) [M + H − H O] , 389 (10) [M +
2
+
+
H − 2 × H O] , 371 (10) [M + H − 3 × H O] , 341 (10) [M + H −
2
2
+
+
+
8
+
4] , 329 (15) [M + H − 96] , 305 (20) [M + H − 120] , 287 (5) [M
+
H − 120 − H O] .
3
2
semiconfluent cultures. For the H-2-DOG uptake experiments, cells
1 h for L6 myocytes, and 3 h for 3T3-L1 adipocytes and C3A
α-Glucosidase Inhibitory Activity. A method for the determi-
(
26
nation of α-glucosidase inhibitory effects was adapted for use on a
BioTek SynergyHT microplate reader with dispenser (BioTek
Instruments, Winooski, VT, USA). A mixture containing α-glucosidase
was extracted from rat intestinal acetone powder (Sigma-Aldrich) by
suspending ca. 350 mg of powder in 10 mL of cold KH PO buffer
hepatocytes) were exposed to 1 and 3-C-β-D-glucopyranosyl-
iriflophenone at concentrations ranging from 0.001 to 100 μM.
Compounds were dissolved in DMSO and diluted with Krebs-Ringer
bicarbonate HEPES buffer (KRBH) containing 8 mM glucose (final
DMSO concentrations <0.004%). For glucose uptake determination,
2
4
(
200 mM KH PO , pH 6.8 with KOH) followed by repeated
2 4
3
cells were pulse-labeled for 15 min with 0.5 μCi/mL H-2-DOG
sonication on ice (sonication sequence repeated 12 times: 30 s
sonication with 25% amplitude, 1 min rest) using a model VCX600
high-intensity ultrasonic processor with a 3 mm stepped microtip
(American Radiolabeled Chemicals, Inc., St. Louis, MO, USA) in
glucose- and serum-free KRBH containing 1 and 3-C-β-D-
glucopyranosyliriflophenone at the relevant concentrations. Insulin
and metformin (1,1-dimethylbiguanide hydrochloride) (Sigma-Al-
drich) both at 1 μM were included as positive and drug reference
(
Sonics & Materials Inc., Newton, CT, USA). The crude mixture was
centrifuged at 10000g for 30 min at 4 °C in a Hettich Universal 320R
refrigerated centrifuge (Hettich Holding GmbH & Co. oHG,
Kirchlengern, Germany), and the supernatant was retrieved and
filtered using 0.45 μm pore size, 33 mm Millex HV PVDF filter
membranes (Merck Millipore). The supernatant was used as an
enzyme mixture after dilution to the standardized concentration based
on activity testing.
3
controls, respectively. The amount of H-2-DOG taken up by cells was
measured using a liquid scintillation counter (2200CA Tricarb Series,
Packard Instrument Company, Downers Grove, IL, USA), and the
3
activity calculated as fmol ( H-2-DOG)/mg protein. Statistical analysis
was performed with GraphPad Prism version 5.00 for Windows using
one-way ANOVA with Dunnett’s multiple comparison post hoc test to
determine significant differences between values at the 95% confidence
level (p < 0.05).
Activity determination of the enzyme mixture was performed daily
prior to each set of experiments, using the same procedure as for the
inhibition assays, but with H O as sample controls and varying
2
dilutions of the enzyme mixture. Fluorescence measurements were
used to determine the correct concentration for optimal enzyme
activity, ca. 15 to 20 mg/mL of the original powder estimated as an
ASSOCIATED CONTENT
■
FL-value of 50 000 (λ : 360 nm; λEM: 460 nm), 20 min after addition
EX
*
S
Supporting Information
of the substrate.
1
13
S1 ( H), S2 ( C), S3 (COSY), S4 (1D NOESY), S5 (HSQC),
The inhibitory activities of 1, 2, 3-C-β-D-glucopyranosyl-
iriflophenone (Fluka, Sigma-Aldrich, St. Louis, MO, USA), and
maclurin (Sigma-Aldrich) were assessed at three concentration levels
ranging between 50 and 400 μM. Acarbose (Sigma-Aldrich), a known
inhibitor of mammalian α-glucosidase, was used as positive control at
and S6 (HMBC) NMR spectra of 3-C-β-D-glucopyranosyl-4-O-
1
β-D-glucopyranosyliriflophenone (1). S7: H NMR spectra for
3-C-β-D-glucopyranosyliriflophenone (obtained by acid hydrol-
ysis of 1), with an overlay of corresponding spectra for the
commercial reference standard. S8: The unreacted product of 1
is also compared to the starting material of 1 to assess the
stability of the sugar moiety during the acid hydrolysis reaction.
This material is available free of charge via the Internet at
http://pubs.acs.org.
65 μM. The following test procedure was employed: 20 μL of the
assay control (H O), positive control, or target analyte at selected
2
concentration was added to 125 μL of a 200 mM KH PO buffer (pH
2
4
6
.8) and 65 μL of the chosen enzyme dilution in 96-well black, flat-
bottom microplates with a clear bottom (Greiner Bio-One GmbH,
Rainbach im Muhlkreis, Austria). The mixture was preincubated at 37
̈
E
dx.doi.org/10.1021/np5007247 | J. Nat. Prod. XXXX, XXX, XXX−XXX

Journal of Natural Products
Article
(
20) Tanaka, T.; Sueyasu, T.; Nonaka, G.-I.; Nishioka, I. Chem.
AUTHOR INFORMATION
Corresponding Author
E-mail: beelderst1@arc.agric.za (T. Beelders). Phone: +27-21-
09-3441. Fax: +27 21-809-3430.
■
Pharm. Bull. 1984, 32, 2676−2686.
21) Li, H.; Song, F.; Xing, J.; Tsao, R.; Liu, Z.; Liua, S. J. Am. Soc.
Mass. Spectrom. 2009, 20, 1496−1503.
22) Zhang, Y.; Qian, Q.; Ge, D.; Li, Y.; Wang, X.; Chen, Q.; Gao, X.;
(
*
8
(
Notes
Wang, T. J. Agric. Food Chem. 2011, 59, 11526−11533.
(23) Zhang, Y.; Liu, X.; Han, L.; Gao, X.; Liu, E.; Wang, T. Food
Chem. 2013, 141, 2896−2905.
The authors declare no competing financial interest.
(
24) Zhou, G.; Myers, R.; Li, Y.; Chen, Y.; Shen, X.; Fenyk-Melody,
J.; Wu, M.; Ventre, J.; Doebber, T.; Fujii, N.; Musi, N.; Hirshman, M.
F.; Goodyear, L. J.; Moller, D. E. J. Clin. Invest. 2001, 108, 1167−1174.
25) Roessner, U.; Wagner, C.; Kopka, J.; Trethewey, R. N.;
ACKNOWLEDGMENTS
■
This work is based on the research supported in part by the
South African Department of Science and Technology (DST/
CON 0133/2012). Other financial support was received
through a grant from the Economic Competitive Support
Package for Agroprocessing to the ARC by the South African
Government. NRF grant holders (E.J. and C.J.M.) acknowledge
that opinions, findings, and conclusions or recommendations
expressed in any publication generated by the NRF-supported
research (IFRR Grant 85277 and Thuthuka Grant 87849) are
those of the authors and that the NRF accepts no liability
whatsoever in this regard. An NRF-DST Professional Develop-
ment Program Doctoral Scholarship to T.B. is acknowledged.
Mr. F. Joubert (Koksrivier) is acknowledged for supplying plant
̈
(
Willmitzer, L. Plant J. 2000, 23, 131−142.
(26) Azuma, T.; Kayano, S.; Matsumura, Y.; Konishi, Y.; Tanaka, Y.;
Kikuzaki, H. Food Chem. 2011, 125, 471−475.
(27) Mazibuko, M. E. In Vitro and in Vivo Effect of Aspalathus
linearis and Its Major Polyphenols on Carbohydrate and Lipid
Metabolism in Insulin Resistant Models. Ph.D. Thesis, University of
Zululand, KwaDlangezwa, South Africa, 2013.
̈
material. Ms. W. Kuhn (Water Analysis Division, CAF,
Stellenbosch University) is thanked for the enzyme robot
assay, and Mr. F. Hiten (Mass Spectrometry Unit, CAF,
Stellenbosch University) for GC-MS analyses.
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dx.doi.org/10.1021/np5007247 | J. Nat. Prod. XXXX, XXX, XXX−XXX