Patent Grant
7109232
The present invention relates to novel mixture and compounds from mycelium of Antrodia Camphorata and the use thereof. The present invention relates to the composition or mycelium comprising the compounds of the invention.
The fruiting body of Antrodia camphorata (Polyporaceae, Aphyllophorales) is well known in Taiwan as a traditional Chinese medicine. It grows only on the inner heartwood wall of the endemic evergreen Cinnamomun kanehirai (Hay) (Lauraceae) in Taiwan. It is rare and has not been cultivated. The fruiting bodies have been used for treating of food and drug intoxication, diarrhea, abdominal pain, hypertension, itchy skin, and liver cancer. Very few biological activity studies have been reported hitherto.
Antrodia camphorata also known as “niu-chang-chih” or “niu-chang-ku” in Taiwan, was recently reported as a new fungus species characterized by the cylindrical shape of its basidiospores appearing in fruiting bodies, weakly amyloid skeletal hyphae, bitter taste and light cinnamon resupinate to pileate basidiocarps, as well as chlamydospores and anthroconidia in pure culture. The growth of this new fungus species is extremely slow and restricted to an endemic tree species, Cinnamomum kanehirai Hay (Lauraceae), as the only host. The detailed characterization and taxonomic position of Antrodia camphorata were described in Wu, S.-H., et al., Antrodia cinnamomea (“niu-chang-chih”), New combination of a medicinal fungus in Taiwan, Bot. Bull. Acad. Sin. 38: 273–275 (1997).
In Taiwanese folk medicine, the fruiting bodies of Antrodia camphorata are believed to have certain medical effects. According to the traditional way, the fruiting bodies are ground into dry powder or stewed with other herbal drugs for oral uptake to treat conditions caused by poisoning, diarrhea, abdominal pain, hypertension, skin itches and liver cancer. However, few pharmacological or clinical study in these aspects has appeared in literature to date. Because of the stringent host specificity and rarity in nature, as well as the failure of artificial cultivation, “niu-chang-chih” is very expensive in Taiwan. In recent years, the fruiting bodies of this fungus with high quality have been sold at an extremely high price of around U.S.$ 15,000 per kg.
Accordingly, an object of the present invention is to provide novel mixture from mycelium of Antrodia Camphorata.
Another object of the present invention is to provide novel compounds from mycelium of Antrodia Camphorata.
Further object of the present invention is to provide novel composition comprising the compounds of the invention.
Further object of the present invention is to provide novel mycelium of Antrodia Camphorata comprising the compounds of the invention.
a)-(d) shows test results of compound 3 of the invention.
a)-(c) shows test results of ACM, (Antrodia camphorata mycelia powder) H2O Extract.
a)-(f) shows test results of ACM EtOH (ethyl alcohol) Extract.
a)-(e) shows test results of compound 1 of the invention.
The present invention provides a compound having the formula
wherein
In the compound of the invention, the preferred R1 is C2-6 alkenyloxy, or C2-6 alkynyloxy; the more preferred R1 is C2-6 alkenyloxy substituted with C1-6 alkyl and the most preferred R1 is butenyloxy substituted with methyl. In the compound of the invention, the preferred R2 is C1-6 alkyl, the most preferred R2 is isobutyl.
Accordingly, the preferred compound of the invention is 3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]furan-2,5-dione, 3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]-1H-pyrrol-2,5-dione, 3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]-1H-pyrrol-1-ol-2,5-dione, 3R*,4S*-1-hydroxy-3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]pyrrolidine-2,5-dione, or 3R*,4R*-1-hydroxy-3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]pyrrolidine-2,5-dione.
The further preferred compound of the invention is 3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]-1H-pyrrol-2,5-dione or 3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]-1H-pyrrol-1-ol-2,5-dione. The further preferred compound of the invention is 3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]-1H-pyrrol-1-ol-2,5-dione.
The present invention also provides a mixture from mycelium of Antrodia Camphorata, which comprises the compound of the invention. The mixture of the invention is prepared from water or organic solvent extract of mycelium of Antrodia Camphorata. The organic solvent includes but is not limited to alcohol (such as CH3OH, C2H5OH, C3H7OH), ester (such as acetyl acetate), alkane (such as hexane) and halogenated alkane (such as CH3Cl, C2H2Cl2). The preferred organic solvent is ethanol or alcoholic solvent without causing any side effect of human. The mixture of the invention can decrease systolic blood pressure or increase high density lipoprotein. In addition, the same mixture has central cholinergic agonism, hepatoprotection, anti-inflammation or anti-tumor activity. Especially, the mixture of the invention can inhibit tumor from the cells or tissues selected from the group consisting of liver, intestine, bone, blood, lymph and breast. The subject accepting the mixture of the invention includes but is not limited to human, mammal, mouse, rat, horse, pig, chicken, duck, dog and cat.
The present invention also provides a composition, which comprises the compound of the invention. The composition of the invention can decrease systolic blood pressure or increase high density lipoprotein. In addition, the composition of the invention has central cholinergic agonism, hepatoprotection, anti-inflammation or anti-tumor activity. Especially, the composition of the invention can inhibit tumor from the cells or tissues selected from the group consisting of liver, intestine, bone, blood, lymph and breast. The subject accepting the composition of the invention includes but is not limited to human, mammal, mouse, rat, horse, pig, chicken, duck, dog and cat.
The present invention also provides novel mycelium of Antrodia comprising the compounds of the invention. The preferred mycelium has at least 1% of the weight of raw mycelium being the total weight of the compounds 1–5 of the invention. The most preferred mycelium has at least 3% of the weight of raw mycelium being the total weight of the compounds 1–5 of the invention. The mycelium of Antrodia Camphorata is previously prepared according to submerged liquid fermentation such as T. L. M. Stamford et al., Food Science “Protein enrichment of cashew wastes for animal feeds” from http://www.unu.edu/unupress/food/8F101e/8F101E0b.htm.
The examples below are non-limiting and are merely representative of various aspects and features of the present invention.
General Experimental Procedures.
Melting points were measured on a Yanagimoto micro hot-stage melting point apparatus and uncorrected. Optical rotations were measured with a Jasco DIP-360 automatic polarimeter. UV spectra were measured with a Shimadzu UV-2200 recording spectrophotometer. IR spectra were measured with a Jasco FT/IR-230 infrared spectrometer. 1H- and 13C-NMR spectrum were measured with a Varian Unity Plus 500 spectrometer. EIMS and HR-EIMS were measured with a Jeol JMS-AX 505 HAD mass spectrometer at an ionization voltage of 70 eV. Column chromatography was carried out on silica gel BW-820 MH (normal phase) and Chromatorex-ODS DM1020T (reversed phase) (Fuji Silysia).
Extraction and Isolation
Antrodia camphorata mycelia powder (ACM) (60 g), from Simpson Biotech Co. Ltd., Taiwan, October 2001, were three times extracted with CHCl3 for 3 h under reflux. The CHCl3 extract (5.3 g) was chromatographed on silica gel eluted with n-hexane-acetone (19:1–14:6), and CHCl3-MeOH (1:1) to give nine fractions (Fr. 1–9). Fraction 2 was chromatographed on silica gel to give compound 1 (8.7 mg). Fraction 4 was chromatographed on normal and reversed phase silica gel to give compound 2 (13.6 mg). Fraction 5 was chromatographed on silica gel eluted with n-hexane-acetone (8:2) to give ergosterol peroxide (35.8 mg). Fraction 6 gave compound 3 (14.6 mg) by combination of normal and reversed phase silica gel column chromatography. Fraction 7 yielded a mixture of compounds 4 and 5 (4:1) by column chromatography. The mixture of compounds 4 and 5 were subsequently separated by preparative HPLC [column: Tosoh TSK-gel ODS-80TM (21.5×300 mm), mobile phase: CH3OH—H2O containing 0.1% TFA (70:30)].
3-Isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]furan-2,5-dione (compound 1):
yellow oil; UV (MeOH) λmax (log ε) 227 (4.1), 258 (3.9), 275 (3.8), 355 (3.4) nm; IR (CHCl3) νmax 1763 cm−1; 1H-NMR Table 1; 13C-NMR Table 2; EIMS m/z 314 [M]+ (100), 246 (100), 131 (100); HR-EIMS m/z 314.1523 (Calcd for C19H22O4, 314.1518).
3-Isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]-1H-pyrrole-2,5-dione (2):
yellow needles (n-hexane-AcOEt); mp 110–111° C.; UV (MeOH) λmax (log ε) 230 (4.3), 272 (3.5), 355 (3.7) nm; IR (CHCl3) νmax 1724 cm−1; 1H-NMR Table 1; 13C-NMR Table 2; EIMS m/z 313 [M]+ (8), 245 (100), 203 (77), 131 (28); HR-EIMS m/z 313.1681 (Calcd for C19H23NO3, 313.1678).
X-ray Crystallography of Compound 2:
Yellow needles were obtained by crystallization from n-hexane-AcOEt and selected for data collection. Crystal data: C19H23NO3; Mr=313.40; dimensions 0.15×0.02×0.02 mm; triclinic, space group P1 (#2), a=6.3505(5) Å, b=12.205(1) Å, c=12.560(2) Å, α=64.623(7)°, β=75.358(4)°, γ=84.681(5)°, V=850.9(2) Å3, Z=2, Dcalc=1.223 g/cm3, μ(MoKα)=0.82 cm−1, F000=336.00. Measurement was made on a Rigaku RAXIS-RAPID Imaging Plate diffractometer with graphite monochromated Mo-Kα (λ=0.71069 Å) radiation at 93 K. Of the 8950 reflections which were collected, 4745 were unique (Rint=0.108); equivalent reflections were merged. The crystal structure was solved by direct methods (SHELXS86) and refined by full-matrix least-squares. The non-hydrogen atoms were refined anisotropically. Hydrogen atoms were included but not refined. The final indices were R=0.074, Rw=0.099, with GOF (Guest Observer Facility)=1.06. The maximum and minimum peaks on the final difference Fourier map corresponded to 0.83 and −0.89 e−/Å3, respectively.
3-Isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]-1H-pyrrol-1-ol-2,5-dione (Compound 3): yellow oil; UV (MeOH) λmax (log ε): 232.5 (4.3), 296 (3.7), 374 (3.7) nm; IR (CHCl3) νmax 1717 cm−1; 1H-NMR Table 1; 13C-NMR Table 2; EIMS m/z 329 [M]+ (12), 261 (100), 131 (50); HR-EIMS m/z: 329.1637 (Calcd for C19H23NO4, 329.1627).
3R*,4S*-1-Hydroxy-3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]pyrrolidine-2,5-dione (4): colorless oil; [α]D23+2.5° (c 0.2, MeOH); UV (MeOH) λmax (log ε): 225 (4.3), 275 (3.3), 283 (3.2) nm; IR (CHCl3) νmax 1715 cm−1; 1H-NMR Table 1; 13C-NMR Table 2; EIMS m/z 331 [M]+(2), 263 (67), 207 (66), 191 (30), 179 (40), 133 (64), 69 (100); HR-EIMS m/z 331.1747 (Calcd for C19H25NO4, 331.1783).
3R*,4R*-1-Hydroxy-3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]pyrrolidine-2,5-dione (5): colorless oil; [α]D23+3.0° (c 0.2, MeOH); UV (MeOH) λmax (log ε): 227 (4.3), 275 (3.4), 283 (3.3) nm; IR (CHCl3) νmax 1715 cm−1; 1H-NMR Table 1; 13C-NMR Table 2; EIMS m/z 331 [M]+ (1), 263 (45), 207 (50), 191 (75), 179 (30), 133 (100), 69 (92); HR-EIMS m/z 331.1766 (Calcd for C19H25NO4, 331.1783).
Ergosterol peroxide: colorless needles (n-hexane-acetone); mp 165–169° C. (lit2 mp 171–174° C.).
Cytotoxic Assays. The in vitro LLC tumor cell assay was carried out by sulforhodamin B (SRB) method. The 50% growth inhibition (ED50) was calculated by Probit method.
Results and Discussion
The CHCl3 extract of the mycelium of Antrodia Camphorata was repeatedly hromatographed on normal and reversed phase silica gel to afford five new maleic and succinic acid derivatives (compounds 1–5) together with ergosterol peroxide.
Table 1
1H-NMR Spectral Data of Compounds 1–5 (δ ppm,
13C-NMR Spectral Data for Compound 1–5 (δ ppm) (125
a)Assignments may be interchangeable.
The structures of the new compounds were determined as follow: Compound 2 gave yellow needles, mp 110–111° C., and the molecular formula C19H23NO3 was assigned by HR-EIMS. The IR spectrum showed an imide carbonyl absorption at 1724 cm−1. The 13C-NMR spectrum showed signals of four methyl carbons, two methylene carbons, and one methine carbon in the aliphatic region, as well as one benzene ring, one olefinic group and two carbonyl carbons. The 1H-NMR spectrum showed the presence of an isobutyl moiety at δ 0 0.90, 2.06, and 2.51, a 3-methyl-2-butenyloxy moiety at δ 1.76, 1.81, 4.56, and 5.50, and a para-substituted benzene moiety at δ 6.95 and 7.50, which was further supported by 1H—1H COSY (cooler synchrotron) and HMQC (heteronuclear multiple quantum coherence) experiments. Long range correlations were observed by HMBC as shown in
The molecular formula of compound 1 was assigned as C19H22O4 by HR-EIMS. The IR spectrum revealed a carbonyl absorption of acid anhydride at 1763 cm−1. The 1H-NMR spectrum of compound 1 was similar to that of compound 2, and showed the presence of an isobutyl moiety, a 3-methyl-2-butenyloxy moiety, and a para-substituted benzene ring. From the HMBC spectrum, compound 1 was demonstrated to have the same partial structure to compound 2 (
The molecular formula of compound 3 was assigned as C19H23NO4 by HR-EIMS. The IR spectrum showed a carbonyl absorption at 1717 cm−1, assignable to a hydroxy imide. The 1H- and 13C-NMR spectra were also similar to those of compounds 1 and 2, and showed the presence of an isobutyl moiety, a 3-methyl-2-butenyloxy moiety, and a para-substituted benzene ring. In the HMBC experiment, compound 3 was shown to have the same partial structure as compound 2 (
Compounds 4 and 5 had the same Rf values and the same molecular formula by HR-EIMS (C19H25NO4, found 331.1747 and 331.1766, respectively), however, they could be separated by preparative HPLC. The IR spectrum of both compounds showed a hydroxy imide carbonyl absorption at 1715 cm−1. In the 1H- and 13C-NMR spectra, both compounds showed the presence of an isobutyl moiety, a 3-metyl-2-butenyloxy moiety, and a para-substituted benzene ring, but the isobutyl methylene protons displayed a multiplet and not a doublet as for compounds 1–3. The 1H-1H COSY spectrum indicated that this methylene group is attached to a —CH—CH— unit. The 13C-NMR spectra of compounds 4 and 5 exhibited two additional sp3 carbon signals, replacing two sp2 carbon signals observed for compounds 1–3. Therefore, compounds 4 and 5 were not N-hydroxy maleimides, but rather N-hydroxy succinimides, with stereocenters at positions C-3 and C-4 in the succinimide ring. Compounds 4 and 5 were determined to be trans and cis isomers, respectively, from the coupling constant between H-3 and H-4 (4.0 and 8.0 Hz for compounds 4 and 5, respectively). No NOE was observed between H-3 and H-4 in the NOESY (Nuclear Overhauser Effect Spectroscopy) spectrum of compound 4, while appreciable NOE was observed in that of compound 5. The optical rotations of compounds 4 and 5 showed +2.5° and +3.0°, respectively, while their CD spectra showed no Cotton effects at any wave length, suggesting that both compounds 4 and 5 are racemic mixtures. Resolution of these racemic mixtures by HPLC using a chiral column with several solvent systems was unsuccessful. At present, we cannot definitely conclude whether these compounds are optically active compounds or racemic mixtures. Thus, their relative structures were determined as 3R*,4S*- and 3R*,4R*-1-hydroxy-3-isobutyl-4-[4-(3-methyl-2-butenyloxy)phenyl]pyrrolidine-2,5-dione, respectively.
Isolation of these type of maleic and succinic acid derivatives from nature were second time followed by the report of Aquveque et al.
The cytotoxic activity of the chloroform extract and isolated compounds were investigated using LLC (Lewis lung carcinoma) cell line (Table 3). The chloroform extract showed moderate cytotoxic effects with an ED50 value of 26.7 μg/ml. Maleic compounds 1 and 4 had no cytotoxic activity, whereas compounds 2 and 3 were found to be cytotoxic to the LLC cell line with ED50 values lower than that of the chloroform extract.
a)Positive control.
Tumor Assay of ACM (Antrodia camphorata Mycelia Powder)
A. Cell line
Suspension cell:
Compound 1, Compound 3, ACM EtOH Extract, ACM H2O Extract
C. Assay method
Calculate ED50 (50% inhibition of effective dose
Adherent cell: MTT (methyl thiazolyl tetrazolium) method; for MCF-7, HT-29, KATO II1, SW480, HepG2, cells are determined at 3 days. SW620 at 4 days
Suspension cell: Cell count method; EL4 cells count at 5 days
D. Result
Calculation:
y=m Ln(x)+b
Use value of X (10, 30, 50 ppm) and Y to get correlation curve
y=−0.2643Ln(x)+1.5321
ED50=exp[(0.97/2−1.5321)/(−0.2643)]
Sample Preparation and Sample Description
A. ACM (Antrodia Camphorata Mycelia Powder) H2O Extract
B. Determination of Sample Concentration
C. ACM (Antrodia Camphorata Mycelia Powder) EtOH Extract
D. Compound 1 Pure compound from ACM
E. Compound 3 Pure compound from ACM
MTT Assay Method
Result and Discussion
Deatiled test results as follows:
Analysis of All New Compounds (1, 2 and 3) from ACM EtOH Extract by High Performance of Liquid Chromatography Method
Purpose: In order to measure the amount of all new compounds (1, 2 and 3) from ACM EtOH Extract, High Performance of Liquid Chromatography was employed as our routine quality control procedures.
Preparation for ACM EtOH Extract Sample
Results: according to HPLC analysis, the extract product contains pure compound 1, 2, and 3 was showed in following Table 4
Therefore, the total weight of compounds 1, 2 and 3 is 5.92% by weight in ACM sample.
Tests for ACM-EtOH Extract
Materials and Equipment
1. Test Substances and Dosing Pattern
Test substance was administered orally at an initial dose of 1000 mg/kg for all in vivo assays in a vehicle of 2% Tween 80. Time of observation for each assay was described in methods.
2. Animals
Male or female ICR mice, Wistar-Okamoto derived male spontaneously hypotensive rat (SHR), Wistar and Long Evans derived rats provided by MDS Pharma Services Taiwan Ltd. were used. Space allocation for animals was as folloes: 29×18×13 cm for 10 mice, 45×23×21 cm for 6 rats, and 45×23×21 cm for 3 guinea pigs. Mice and rats were housed in APECR cages. The immunocompetent C57BL/6J male mice, 6–8 weeks age, weighing 21±2 gm were also used in this study and provided by National Taiwan University Animal Center. The animals were housed in Individually Ventilated Cages Racks (IVC racks, 36 Mini Isolator System). Each cage was sterilized by autoclave and contained 5 mice (in 26.7×20.7×14 cm). All animal were maintained in a controlled temperature (21°–23° C.) and humidity (60%–70%) environment with 12 hour light dark cycles for at least one week in the laboratory prior to use. Free access to standard lab chow (LabDiet Rodent Diet and Guinea Pig Diet, PMI Nutrition International, USA) and tap water was granted.
3. Cell Line and Culture Media
The murine melanoma cell line, B16-F0 (ATCC CRL-6322), was purchased from American Type Culture Collection and Dulbecco's Modified Eagle's Medium (GIBCO, USA) was used as culture medium. The tumor cells were incubated in an atmosphere containing 5% CO2 at 37° C.
4. Chemicals
General:
Distilled Water (In-house), Dimethyl Sulfoxide (DMSO, Merck, Germany), Isotonic Sodium Chloride Solution (Sintong Chemical Industry Co. Ltd., R.O.C.), magnesium Sulfate (MgSO4.7H2O, Wako, Japan), Meclofenamate Sodium (Sigma, USA), Methylcellulose (Signa, USA), Sodium Hydroxide (NaOH, Wako, Japan), Phosphate Buffered Saline (Sigma, USA) and Tween 80 (Wako, Japan).
Reagents
Glicose-HA assay kit (Wako, Japan), Alanine aminotransferase (ALT) assay kit (Wako, Japan), Aspartate aminotransferase (AST) assay kit (Wako, Japan), T-Cholesterol-HA and HDL assay kit (Wako, Japan), Hemolynac 3 Hemolys (Nihon Koden, Japan), Isotonic 3 Diluent (Nihon Koden, Japan).
5. Equipment
General Use:
Animal Case (ShinTeh, R.O.C.), Beaker 250 ml and 1000 ml (Kinmax, USA), disposable syringe (1 ml, Top Corporation, Japan), Forceps stainless (klappencker, Germany), Mouse scale #Z-40 (Taconic, USA), needle for oral administration (Natsune, Japan), Needle Hypodermic 23 G×1″ (Top Corporation, Japan), pH Meter (Suntex, USA), Rat scale 500 g±2 g (Chien-chun, ROC), syringe Glass 1 ml, 2 ml and 5 ml (Mitsuba, Japan), and Scissors Stainless (Klappencker, Germany).
Methods and Results:
Test substance was administered orally to a group of 3 Wistar derived male or female rats weighing 150±20 g. During the subsequent 30–60 minute period, the number of animals exhibiting more than 10 seconds of chewing behavior (mouth and/or tongue movements) measured cumulatively and the number of animals exhibiting salivation or exhibiting salivation were noted. Positive responses observed in 2 or more (≧2) of 3 rats indicates possible central cholinergic activity and peripheral cholinergic activity.
Vehicle and test substances were administered orally (PO) while the positive reference compound was injected intraperitoneally (IP). During the subsequent 30–60 minute period, the number of animal exhibiting more than 10 seconds of chewing behavior (mouth and/or tongue movements) measured cumulatively or exhibiting salivation were noted. Positive responses observed in 2 or more (≧2) of 3 rats indicates possible cholinergic activity or peripheral cholinergic activity.
Groups of 3 Wistar-Okamoto derived male spontaneously hypertensive rats (SHR) weighting 250±20 g were used; the mean systolic blood pressure was 200±20 mmHg and heart rate 400±30 beats/min. Blood pressure and heart rate were recorded indirectly by tail cuff method in a temperature controlled environment (32±1° C.) before (0 time) and 1, 2 and 4 hours after oral administration of test substance or vehicle. A reduction in systolic pressure by 10 percent or more (≧10%), or decrease in heart rate by 20 percent or more (≧20%), at each measured time interval relative to 0 time, is considered significant.
SHR with systolic blood pressure of 200±20 mmHg and heart rates of 400±50 mmHg Beats/min were used. Blood pressure was recorded indirectly vial tail cuff at 0 time (before) and 1, 2 and 4 hours after oral administration of vehicle or test substance. A reduction in blood pressure by 10 percent or more (≧10%), or decrease in heart rate by 20 percent or more (≧20%) at each measurement time point relative to 0 time, shown in parenthesis, is considered significant.
SHR with systolic blood pressure of 200±20 mmHg and heart rates of 400±50 mmHg Beats/min were used. Blood pressure was recorded indirectly vial tail cuff at time 0 (before) and 1, 2 and 4 hours after oral administration of vehicle or test substance. A reduction in blood pressure by 10 percent or more 10%), or decrease in heart rate by 20 percent or more (≧20%) at each measurement time point relative to 0 time, shown in parenthesis, is considered significant.
Groups of 5 ICR derived male mice weighing 22±2 g were kept on a high fat diet (g/100 g: coconut oil, 8; cholesterol, 1.0; cholic acid, 0.3; lard 2; standard chow 88.7) for 7 days to induce hypercholesterolemia. Test substance was administered orally on days 5, 6 and 7. After fasting overnight, serum was obtained from each mouse and assayed for total cholesterol (Total), high density lipoprotein (HDL) and percent change in Total/HDL. A decrease of 20 percent or more (≧20%) in serum Total or increase of 20 percent or more (≧20%) in serum HDL or decrease of 40% or more (≧40%) in the Total/HDL ratio relative to vehicle treated control animals is considered significant.
Vehicle, test substance or reference positive compound was administered orally (PO) on days 5, 6 and 7 after being fed a high cholesterol diet. Twenty-four hours after the third dose, the overnight-fasted test animals were sacrificed for assessing serum total cholesterol (Total) and high density lipoprotein (HDL). Decrease of 20 percent or more (≧20%) in serum Total or increase of 20 percent or more (≧20%) in serum HDL or decrease of 40% or more (≧40%) in the Total/HDL ratio is considered significant.
Groups of 5 Wistar derived male rats weighing 200±20 g were used. Each animal was treated with a single injection of D-galactosamine (500 mg/kg, IP) Test substance was administered orally at 0.5 hour before and 4 hours as well as 8 hours after D-galactosamine administration and animals were sacrificed 24 hours later. Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels were measured by an optimized UV method with HITACHI automatic analyzer (model 7050). Reduction in ALT or AST activity by 30 percent or more (≧30%), relative to the vehicle treated control animal indicates significant protection.
Test substance and vehicle administered orally at 0.5 hour before and 4, 8 hours after a single dose of galactosamine (500 mg/kg, IP). The rats were sacrificed 24 hours after galactosamine injection and the ALT and AST values were determined. A reduction of ≧30% in the ALT and AST relative to the vehicle group is considered significant.
A group of 3 Long Evans derived male or female overnight fasted rats weighing 150±20 g was fasted overnight prior to study. Test substance was administered orally one hour before right hind paw received injection of carrageenan (0.1 ml of 1% suspension intraplantar). Hind paw edema, as a measure of inflammation, was recorded 3 hours after carrageenan administration using a plethysmometer with water cell (25 mm diameter). Reduction of hind paw edema by 30 percent or more (≧30%) indicates significant acute anti-inflammatory activity.
Vehicle or test substance was administered to overnight fasted rats one hour before right hindpaw (R.P.) injection of carrageenan (0.1 ml of 1% suspension intraplantar); the left hindpaw (L.P.) was not injected. Reduction of hindpaw edema by 30 percent or more (≧30%), shown in parenthesis, indicates significant acute anti-inflammatory activity.
Groups of 5 immunocompetent (6–8 weeks old), pathogen-free (SPF) C57BL/6J male mice bred in an animal isolator (IVC racks) under specific pathogen free (SPF) condition were used. Viable B16-F0 murine melanoma cells (ATCC CRL-6322, 1.0×105 in 0.2 ml), syngeneic for C57BL/6J mice, were injected subcutaneously into dorsal side of experimental mice. Treatment begins 24 hours after tumor inoculation and test compound was administered daily by oral gavage for 21 days, or less when overt signs of toxicity are seen. The mice were monitored for body weight, tumor size and survival starting from day 1 to day 22. Moreover, the tested mice were monitored for survival till the end of the study on day 45.
Tumor weight (mg) was estimated according to the formula for a prolate ellipsoid: length (mm)×[width (mm)]2×0.5, assuming specific gravity to be one and π to be three. Tumor growth in compound treated animals was calculated as T/C (Treatment/Control)×100%; a value of T/C≦42% was considered significant in demonstrating antitumor activity.
The mean survival time of T/C (Treatment/Control) is ≧125% is also considered significant in demonstrating antitumor activity.
Vehicle and test substance were administered to test animals every day at 24 hours after tumor cells implantation for a total of 21 doses. Concurrently, the reference compound, mitomycin, was administered IP twice a week for a total of 6 doses. Tumor size was measured and recorded twice a week for a period of 22 days. Tumor growth inhibition was calculated as T/C (treatment/control)×100. A T/C value of ≦42% was considered significant in demonstrating antitumor activity.
Vehicle and test substance were administered to test animals every day at 24 hours after tumor cells implantation for a total of 21 doses. Concurrently, the reference compound. Tumor size was administered IP twice a week for a total of 6 doses. Tumor size was measured and recorded twice a week for a period of 22 days. The Student's t test was used to determine the siginifcant difference in the change of body weight between test compound and vehicle control group.
45a
45a
The treated mice were monitored for survival through the end of the study on day 45 od the day when test animal died. The mean survival time of T/C (Treatment/Control)≧125% is also considered significant in demonstrating anti-tumor activity.
Discussion:
ACM-EtOH Extract, administered orally (PO), in accordance with in-house established criteria, caused significant activities in the following mouse and rat assays:
Central cholinergic agonism at 1000 mg/kg in rats; a minimum and non-significant agonism was seen a 300 mg/kg; no significant agonism or antagonism on peripheral cholinergic nerve was seen at 1000 mg/kg (Table 5)
Decrease in systolic blood pressure (16%, 12% and 20% at respective 1, 2 and 4 hours observation time points vs. 100% with 0 time) and associated moderate but non-significant decrease in heart rate at 1000 mg/kg in spontaneously hypertensive (SH) rats (Tables 6 and 7); dose of 300 mg/kg did not cause significant changes in systolic blood pressure nor the heart rate (Tables 8 and 9)
Increase in high density lipoprotein (HDL, 39% over vehicle control) at 1000 mg/kg in diet-induced mice (Table 10); the associate total cholesterol (Total) did not change significantly, while the HDL/total ratio was decreased to near significant 31%; dose of 300 mg/kg did not cause significant changes in Total, HDL and HDL/Total ratio (Table 10).
Hepatoprotection (44% decrease in ALT and 57% decrease in AST vs. vehicle control) from galactosamine induced hepatic injury in rats at 1000 mg/kg×3; moderate decrease of 20% in ALT and of 28% in AST at 300 mg/kg×3 was seen (Table 11)
Anti-inflammation (45% inhibition vs. vehicle control) versus carrageenan-induced paw edema in rats at 1000 mg/kg (Table 12); the lower level of 300 mg/kg did not demonstrate significant activity (3% inhibition vs. vehicle, Table 13)
Anti-tumor activity in syngeneic melanoma B16-F0 cell for C57BL/6J mice on day 8, 11 and 15 (Tables 14 and 15) as well as prolongation in animal survival time at 1000 mg/kg (Table 17); animal body weight did not change significantly (Table 16).
Tests for ACM, ACM-ETOH Extract and Compound 3 of the Invention Nine groups of ICR derived male mice (weighing 22±2 g) of 5 each were used.
Each animals was challenged with a single dose of carbon tetrachloride (CCl4, 0.1 ml/kg in 50% olive oil, PO). The test substance of ACM at doses 300 and 1000 mg/kg or compound 3 of the invention at doses 30, 100 and 300 mg/kg were administered orally at 30 minutes before and 4, 8 hours after CCl4 challenge; whereas ACM-ETOH Extract at 300 and 1000 mg/kg administered orally was pretreated one day (twice a day) and 30 minutes before and 4, 8 hours after carbon tetrachloride The animals were sacrificed 24 hours after CCl4. Alanine aminotransferase (ALT) and Aspartate aminotransferase (AST) levels were measured by optimized UV method using a HITACHI automatic analyzer (model 7050). A reduction of ALT or AST levels by 30 percent or greater (≧30%), relative to the vehicle group, indicating significant protection from hepatic injury.
Results
Discussion:
ACM, ACM-EtOH Extract and compound 3 of the invention were evaluated for possible protective activity from hepatic injury induced by carbon tetrachloride in ICR mice. The test substance of ACM at doses 300 and 1000 mg/kg and compound 3 of the invention at doses 30, 100 and 300 mg/kg were administered orally to test animals 0.5 hour before and 4, 8 hours after CCl4 challenge. For ACM-EtOH Extract at 300 and 1000 mg/kg, 2 times (b.i.d.) of treatment (9:00 AM and 16:00 PM) were done 1 day before CCl4 and followed 0.5 hr before and 4, 8 hours after CCl4 challenge (5 dosing in total). The degree of hepatic injury was determined by increase in serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels relative to the vehicle treated animals. ACM at 1000 mg/kg×3 and compound 3 of the invention at 300 mg/kg×3 caused a significant reduction of ALT (46% and 41%) and AST (36% and 33%) relative to the vehicle treated animals. Simultaneously, ACM-EtOH Extract at 300 and 1000 mg/kg×5 also caused significant reduction in ALT (36% and 34%) and AST (25% and 20%).
Concurrently tested silymarin (100 mg/kg×3, IP) showed significantly reduction of ALT (31%) and AST (31%) relative to the vehicle treated group.
It is concluded that ACM, ACM-EtOH Extract and compound 3 of the invention possess the ability of significant hepatoprotectant activity in a mouse CCl4 model.
While the invention has been described and exemplified in sufficient detail for those skilled in this art to make and use it, various alternatives, modifications, and improvements should be apparent without departing from the spirit and scope of the invention.
One skilled in the art readily appreciates that the present invention is well adapted to carry out the objects and obtain the ends and advantages mentioned, as well as those inherent therein. The cell lines, embryos, animals, and processes and methods for producing them are representative of preferred embodiments, are exemplary, and are not intended as limitations on the scope of the invention. Modifications therein and other uses will occur to those skilled in the art. These modifications are encompassed within the spirit of the invention and are defined by the scope of the claims.
It will be readily apparent to a person skilled in the art that varying substitutions and modifications may be made to the invention disclosed herein without departing from the scope and spirit of the invention.
All patents and publications mentioned in the specification are indicative of the levels of those of ordinary skill in the art to which the invention pertains. All patents and publications are herein incorporated by reference to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference.
The invention illustratively described herein suitably may be practiced in the absence of any element or elements, limitation or limitations, which are not specifically disclosed herein. The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention that in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed. Thus, it should be understood that although the present invention has been specifically disclosed by preferred embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention as defined by the appended claims.
Other embodiments are set forth within the following claims.
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| Number | Date | Country | |
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| 20050197384 A1 | Sep 2005 | US |
