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Lignan complex derived from flaxseed as hypercholesterolemic and anti-atherosclerotic agent |
| RE40837 |
Lignan complex derived from flaxseed as hypercholesterolemic and anti-atherosclerotic agent
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| Patent Drawings: | |
| Inventor: |
Prasad |
| Date Issued: |
July 7, 2009 |
| Application: |
11/322,204 |
| Filed: |
December 29, 2005 |
| Inventors: |
Prasad; Kailash (Saskatoon, CA)
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| Assignee: |
Archer-Daniels-Midland Company (Decatur, IL) |
| Primary Examiner: |
Jiang; Shaojia Anna |
| Assistant Examiner: |
Henry; Michael C |
| Attorney Or Agent: |
K&L Gates LLP |
| U.S. Class: |
514/25; 530/500; 536/128; 536/4.1 |
| Field Of Search: |
514/25; 536/4.1; 536/128; 530/500 |
| International Class: |
C07H 15/00 |
| U.S Patent Documents: |
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| Foreign Patent Documents: |
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| Other References: |
Gura (Science, 1997, 278(5340):1041-1042. cited by examiner.
MacRae, W. Donald and Towers, G.H. Neil, Biological Activities of Lignans, Phytochemistry, vol. 23, No. 6, pp. 1207-1220 (1984). cited by examiner.
Bakke, Jerome E. and Klosteman, Harold J., Proc. N. Dak. Acad. of Science, 10, 18-22 (1956). cited by examiner. |
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| Abstract: |
A method is described for treating hypercholesterolemic atherosclerosis or for reducing total cholesterol while raising high-density lipoportoein cholesterol. It involves administering to a patient a substantially pure complex derived from flaxseed and containing secoisolariciresinol diglucoside (SDG), cinnamic acid glucosides and hydroxymethyl glutaric acid. |
| Claim: |
What is claimed is:
1. A method for treating hypercholesterolemic atherosclerosis or for reducing total cholesterol while raising high-density lipoprotein cholesterol which comprisesadministering to a .[.patient an effective amount of.]. .Iadd.human or non-human animal a composition comprising .Iaddend.a .Iadd.substantially pure .Iaddend.complex .[.having a purity of at least 95%.]. derived from flaxseed and containing about 34 to37% by weight secoisolariciresinol diglucoside (SDG), about 13 to 21% by weight cinnamic acid glucosides and about 9.6 to 11.0% by weight hydroxymethyl glutaric acid.
2. .[.A.]. .Iadd.The .Iaddend.method according to claim 1.Iadd., .Iaddend.wherein the cinnamic acid glucosides include coumaric acid glucoside and ferulic acid glucoside.
.Iadd.3. The method according to claim 1, wherein the substantially pure complex is greater than 95% pure..Iaddend.
.Iadd.4. The method according to claim 1, wherein the substantially pure complex has a nominal molecular weight of about 30,000 to 100,000..Iaddend.
.Iadd.5. A method for reducing or treating hypercholesterolemic atherosclerosis, comprising: administering a composition comprising a complex comprising up to 50% secoisolariciresinol diglucoside, up to 25% cinnamic acid glucosides and up to10% hydroxymethyl-glutaric acid to a human or non-human animal; wherein the complex is capable of reducing serum cholesterol in the mammal upon oral administration of a daily dose of 20-60 mg of the complex per kg body weight of the mammal..Iaddend.
.Iadd.6. The method according to claim 5, wherein the composition takes a form selected from the group consisting of a tablet, a capsule, and a food..Iaddend.
.Iadd.7. The method according to claim 5, further comprising extracting the complex from flaxseed..Iaddend. |
| Description: |
BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to a method for the use of a lignan complex isolated from flaxseed for the treatment of atherosclerosis, e.g. reducing or preventing the development of hypercholesterolemic atherosclerosis, for reducing total cholesteroland for raising HDL-C in blood.
2. Description of the Prior Art
Hypercholesterolemia is a major risk factor for atherosclerosis (narrowing of the artery due to deposition of fat in the arterial wall) and related occlusive vascular diseases such as heart attack, stroke and other peripheral vascular diseases. Heart disease is the number one killer. Hypercholesterolemic atherosclerosis has been reported to be associated with oxidative stress increase in levels of reactive oxygen species (ROS), production of ROS by polymorphonuclear leukocytes as assessed bychemiluminescence (PMNL-CL), and a decrease in the antioxidant reserve. Pretreatment with antioxidants (vitamin E, probucol, garlic, purpurogallin, secoisolariciresinol diglucoside) reverses the effects of hypercholesterolemia. Flaxseed which is a richsource of .alpha.-linolenic acid and richest source of plant lignans has been shown to be effective in reducing hypercholesterolemic atherosclerosis without lowering serum levels of cholesterol. Using flaxseed which has very low .alpha.-linolenic acid,has shown that antiatherogenic activity of flaxseed is not due to .alpha.-linolenic acid but may be due to lignan component of flaxmeal.
Presently the treatment of hypercholesterolemia and hypercholesterolemic atherosclerosis is to reduce hypercholesterolemia by using various lipid lowering agents such as bile acid sequestrant (cholestyramine, colestipol), nicotinic acid, HMG-CoAreductase inhibitor (lovastatin, provastatin, simvastatin, fluvastatin and atrovastatin) and gemfibrozil. Recently probucol which has both antioxidant and lipid lowering activity and vitamin E which has antioxidant activity have been used to preventatherosclerosis and restenosis.
Drugs used for lowering serum lipids and for treatment of atherosclerosis (heart attack and stroke) have many side effects and are expensive. Fibric acid derivatives (gemfibrozil) produces gall stones, myopathy and hepatomegaly. Nicotinic acidproduces gastrointestinal symptoms, flushing, hyperglycemia, hepatic dysfunction, elevated uric acid, abnormal glucose tolerance, and skin rash. Bile acid sequestrant (cholestyramine, colestipol) produces gastrointestinal symptoms, and high serum levelsof very low density-lipoprotein (VLDL). HMG-CoA reductase inhibitors (statin) produce gastrointestinal symptoms, myopathy and hepatotoxicity. Probucol produces diarrhea and decreases the serum levels of HDL (good cholesterol).
Prasad, U.S. Pat. No. 5,846,944, describes the use of secoisolariciresinol diglucoside (SDG), isolated from flaxseed, for reducing hypercholesterolemic atheroscleorsis and reducing serum cholesterol. However, isolating SDG from flaxseed is arelatively expensive procedure.
In Westcott et al., U.S. Pat. No. 6,264,853, a new lignan complex is described which has been isolated from flaxseed. This lignan complex typically contains SDG (35%), cinnamic acid glycosides and hydroxymethyl glutaric acid. Only a simpleprocedure is required to isolate this lignan complex from flaxseed.
The purpose of the present invention is to provide a method of using the above lignan complex derived from flaxseed for medical purposes.
SUMMARY OF THE INVENTION
In accordance with this invention, it has been found that a lignan complex isolated from flaxseed can safely be administered to humans or non-human animals for the treatment of a variety of diseases. The complex and a method for its productionare described in Westcott et al., U.S. Pat. No. 6,264,853, issued Jul. 24, 2001, .Iadd.assigned to Agriculture and Agri-Food Canada, .Iaddend.and incorporated herein by reference. .Iadd.The assignee of U.S. Pat. No. 6,264,853 and the assignee ofthe invention disclosed herein were parties to a joint research agreement. .Iaddend.This complex is used in substantially pure form, e.g. a purity of at least 95%, and contains secoisolariciresinol diglucoside (SDG), cinnamic acid glucosides andhydroxymethyl glutaric acid. .Iadd.The complex is substantially pure form comprising SDG, cinnamic acid glucosides and HMGA is a novel material which can be used as is or in the form of a liquid or powder. The powder may contain up to 50% SDG, up to25% total cinnamic acid glucosides and up to 10% HMGA, with less than 1% nitrogen. .Iaddend.It typically has a nominal molecular weight in the range of about 30,000 to 100,000. The complex can be administered orally or intraperitoneally and has beenfound to be highly effective when administrated in a daily oral dosage of 20 to 60 mg per kg of body weight. The oral doses may conveniently be in the form of tablets or capsules and the complex may be used together with a variety of pharmaceuticallyacceptable diluents or carriers.
When administered to humans or non-human animals, the complex has been found to be highly effective for treating hypercholesterolemic atherosclerosis, as well as for reducing total cholesterol and raising HDL-C in blood. Thus, it is useful forthe prevention and treatment of coronary artery disease, stroke and other peripheral vascular diseases.
BRIEF DESCRIPTION OF THE DRAWINGS
In the drawings which illustrate the present invention:
FIG. 1 is a graph showing sequential changes in serum triglyceride concentration for four different experimental groups;
FIG. 2 is a graph showing sequential changes in serum total cholesterol concentration of four different experimental groups;
FIG. 3 is a graph showing sequential changes in serum LDL-C concentration for four different experimental groups;
FIG. 4 is a graph showing sequential changes in serum HDL-C concentration for four different experimental groups;
FIG. 5 is a bar graph showing sequential changes in serum malondialdehyde (MDA) for four different experimental groups;
FIG. 6 is a bar graph showing aortic tissue malondialdehyde (MDA) concentration for four different experimental groups;
FIG. 7 is a bar graph showing aortic tissue chemiluminescence (Aortic-CL) for three different experimental groups;
FIG. 8 shows photographs of endothelial surfaces of aortas for four different experimental groups; and
FIG. 9 is a bar graph showing the extent of atherosclerotic plaques in the initial surface of aorta for four different experimental groups.
In the graphs, the results are expressed as mean.+-.S.E. The symbols used in FIGS. 1 to 5 have the following meanings. *P<0.05, Comparison of values at different times with respect to time "0" in the respective group. .sup.aP<0.05,Control vs other groups. .sup.bP<0.05, Lignan complex vs 0.5% cholesterol or 0.5% cholesterol+lignan complex. .sup.cP<0.5% Cholesterol vs 0.5% cholesterol+lignan complex. .sup.+P<0.05, Month 1 vs month 2 in the respective groups.
In FIGS. 6 and 7 the symbols have the following meanings: *P<0.05, control Vs other groups; .dagger.P<0.05, lignan complex Vs 0.5% cholesterol or 0.5% cholesterol+lignan complex. .sup.aP<0.05, 0.5% cholesterol Vs 0.5% cholesterol-lignancomplex.
For FIG. 7, the significance symbols are as follows: *P<0.05, control Vs other groups. .dagger.P<0.05, 0.5% cholesterol Vs 0.5% cholesterol+lignan complex.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The complex used according to this invention typically contains about 34 to 37% by weight of SDG, about 15 to 21% by weight cinnamic acid glucosides and about 9.6 to 11.0% by weight hydroxmethyl glutaric acid. The cinnamic acid glycosidesinclude coumaric acid glucoside and ferulic acid glucoside. They are typically present in the complex in amounts of about 9.5 to 16.0% by weight coumaric acid glucoside and 4.5 to 5.0% ferulic acid glucoside.
The complex composition typically contains about 59 to 70% by weight of the above active ingredients. The balance comprises protein, ash and water of crystallization.
The invention is further illustrated by the following non-limiting examples.
EXAMPLE 1
EXPERIMENTAL PROTOCOL
Experiments were conducted on New Zealand White rabbits. Rabbits were assigned to 4 groups as shown in Table 1. Those in Group 1 were fed rabbit laboratory chow diet. The other groups received lignan complex or cholesterol orcholesterol+lignan complex. The lignan complex was obtained from Agriculture and Agri-Food Canada and was extracted from flaxseed by the method described in Westcott et al., U.S. Pat. No. 6,264,853incorporated herein by reference. The diet wasespecially prepared by Purina and did not contain any antioxidant. Lignan complex was given orally daily in the dose of 40 mg/kg body weight. The rabbits were cared for according to approved standards for laboratory animal care. The rabbits were ontheir respective diet treatment for 2 months.
Blood samples were collected (from ear marginal artery) for measurement of serum-triglycerides (TG), total cholesterol. (C), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), enzymes, albumin, creatinine,and malondialdehyde (MDA) before (0 time) and after 1 and 2 months on the respective experimental diets. The rabbits were anesthetized at the end of 2 months and aortas were removed for assessment of atherosclerotic plaques, and measurement of aortictissue MDA and antioxidant reserve (Aortic-chemiluminescence). The measurement of lipids, atherosclerotic plaques, oxidative stress were done according to known methods. Serum enzymes, albumin and creatinine for assessment of liver and kidney functionwere measured by already established techniques. Assessment of hemopoietic system were made by established techniques available in the hospital.
SERUM LIPIDS. Changes in serum TG, C, LDL-C, and HDL-C in the 4 groups are shown in FIGS. 1-4. Lignan complex did not affect serum TG, TC, LDL-C but increased HDL-C significantly in the groups on control diet. A 0.5% cholesterol diet increasedserum TG, C, LDL-C and HDL-C. Lignan complex in 0.5% cholesterol-fed rabbit produced less increase in C and LDL-C, and greater increase in HDL-C as compared to only 0.5% cholesterol-fed rabbits. Serum TG levels were similar in Group III and IV.
These results indicate that the lignan complex lowers serum cholesterol (significantly) and LDL-C (not significant), and raises HDL-C (significantly) in hypercholesterolemic rabbit. Lignan complex also raises HDL-C in normocholesterolemicrabbits.
OXIDATIVE STRESS. Results for oxidative stress parameters (serum MDA, aortic tissue-MDA, aortic tissue antioxidant reserve) are shown in FIGS. 5-7. Serum MDA levels remained unaltered in control and lignan complex groups. It increased in both0.5% cholesterol and 0.5% cholesterol+lignan groups. However, the increase was less in groups with 0.5% cholesterol+lignan complex. Aortic MDA increased and lignan complex decreased in 0.5% cholesterol-fed rabbits. Aortic tissue chemiluminscence(Aortic-CL) is a measure of antioxidant reserve. An increase in Aortic-CL suggests a decrease in the antioxidant reserve and vice-versa. Aortic-CL decreased in cholesterol-fed group of rabbits. Lignan complex in cholesterol-fed rabbits tended toincrease the aortic-CL compared to 0.5% cholesterol without lignan complex.
These results indicate that high cholesterol increases oxidative and the lignan complex reduces oxidative stress.
ATHEROSCLEROSIS. Representative photographs of endothelial surfaces of aortas from each group are depicted in FIG. 8, and the results are summarized in FIG. 9. In FIG. 8, Group I is Control, Group II is lignan complex, Group III is 0.5%cholesterol and Group IV is 0.5% cholesterol+lignan complex. In FIG. 9: *P<0.05Group I or Group II vs Group III and Group IV. .dagger.P<0.05, Group III vs Group IV. Atherosclerotic plaques were absent in Group I and II. However, a significantarea of aortic surface from Group III (50.84.+-.6.23%) and Group IV (33.40.+-.4.80%) was covered with atherosclerotic plaques.
This indicates that the lignan complex reduced the hypercholesterolemic atherosclerosis by 34.3%.
HEMOPOIETIC SYSTEM
Red Blood Cells (RBCs). The changes in various parameters related to RBC are shown in Tables 2-8. In general lignan complex in the control diet group (Group II) did not affect the RBC count, hemoglobin (Hb), hematocrit (Hct), mean corpuscularvolume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC) and red blood cell distribution width (RDW). Cholesterol diet (Group III) alone produced significant decreases in RBC, Hb, Hct and MCH; increases in RDW;and no change in MCV and MCHC. Lignan complex in 0.5% cholesterol-fed rabbits (Group IV) reduced RBC, Hb, and Hct; increased MCV, MCH and RDW. The values for RBC, Hb, Hct, MCV, MCH, MCHC and RDW in Group IV were not significantly different from thosein Group III. This shows that, in general, the lignan complex has no adverse effects on the hemopoietic system.
White Blood Cells. The changes in the white blood cells (WBCs) and the differential counts granulocytes, lymphocytes, and monocytes are shown in Tables 9-12. Lignan complex in the control diet group (Group II) produced decreases in WBCs andmonocytes, and no changes in granulocytes and lymphocytes. These changes in the various parameters in Group II were not significantly different from those in control group (Group I). These parameters of WBCs were unaffected in Group III and IV exceptin Group III where monocyte counts decreased.
These results indicate that lignan complex has no adverse effects on the WBCs, granulocytes, lymphocytes and monocyte counts.
PLATELET. The changes in platelet counts and mean platelet volume (MPV) of the four groups are summarized in Tables 13-14. Platelet counts slightly decreased in Group I but MPV remained unchanged. These parameters remained unaltered in GroupII. Basically, all the parameters in all the groups remained unaltered. These results indicate that lignan complex has no adverse effects on platelet counts and mean platelet volume.
EXAMPLE 2
Studies were conducted to determine if the lignan complex given for 2 months produces adverse effects on liver and kidney function.
(a) Assessment of liver function was made by measuring serum enzymes [alkaline phosphatase (ALP), alanine amino-transferase (ALT), aspartate aminotransferase (AST) and gamma-glutamyltransferase (GGT)] and serum albumin. These serum enzymes areelevated and serum albumin is decreased in liver disease. The results are summarized in Table 15-19. Serum levels of ALT, AST and GGT were similar in Groups I and II at month two of the protocol, however levels of serum ALP were lower in Group IIcompared to Group I. The changes in the serum levels of ALP, ALT and GGT remained unchanged as compared to "0" month in the Groups III and IV. However serum levels of AST increased to a similar extent in both groups III and IV. Serum albumin levelsincreased at month one as compared to "0" month in all the groups, however the increases at month two were not significantly different as compared to "0" month. The values of serum albumin at month two, although higher in Groups I and II as compared toGroup III and IV, they were not significantly different from each other.
These results indicate that hypercholesterolemia has adverse effects on liver function and that the lignan complex does not have adverse effects on liver function.
(b) Assessment of kidney function was made by measuring serum enzymes (ALT and AST) and creatinine. ALT, AST and creatinine levels are elevated in dysfunctional kidney. The results are summarized in Tables 16, 17 and 20.
There were no significant differences in the values of serum ALT, AST and creatinine among the 4 groups.
These results indicate that the lignan complex or hypercholesterolemia did not have adverse effects on kidney function.
EXAMPLE 3
The lignan complex was also fed orally to normal ratsfor 2 months at a daily dosage of 40 mg/kg of body weight and the rats were studied to see if the complex had any affect on the liver and kidney function and hemopoietic cells. It was foundthat the lignan complex did not affect any of the above, indicating that it is not toxic to liver, kidney and blood cells.
TABLE-US-00001 TABLE 1 Experimental Diet Groups Group Diet/Treatment I (n = 10) Control (Rabbit chow diet) II (n = 6) Lignan complex control (Rabbit chow diet supplemented with lignan complex, 40 mg/kg body weight, orally, daily) III (n = 12)Cholesterol diet (0.5% cholesterol in rabbit chow diet) IV (=16) Cholesterol diet + lignan complex (0.5% cholesterol diet supplemented with lignan complex, 40 mg/kg; body weight, orally, daily)
TABLE-US-00002 TABLE 2 Red Blood Cells (RBC) Counts (10.sup.12/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 5.08 .+-. 0.12.sup. 6.22 .+-. 0.18* 6.04 .+-. 0.16* .sup. II. Control diet + 5.76 .+-. 0.16.sup.a 6.03.+-. 0.13 5.90 .+-. 0.20 .sup. lignan complex III. 0.5% cholesterol 5.67 .+-. 0.07.sup.a 5.61 .+-. 0.09*.sup.,b 4.60 .+-. 0.11*.sup.,.dagger.,a,b diet IV. 0.5% cholesterol 5.83 .+-. 0.09.sup.a 5.43 .+-. 0.06*.sup.,a,b 4.70 .+-. 0.14*.sup.,.dagger.,a,b diet + lignan complex *P < 0.05, 0 month vs 1 and 2 months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups. .sup.bP < 0.05, GroupII vs Group III or Group IV.
TABLE-US-00003 TABLE 3 Hemoglobin Levels in the Blood (g/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 111.8 .+-. 1.6.sup. 133.8 .+-. 4.2*.sup. 128.9 .+-. 2.5* II. Control diet + 126.8 .+-. 2.2.sup..dagger. 134.6 .+-. 2.4*.sup. 129.0 .+-. 3.1 lignan complex III. 0.5% cholesterol 125.1 .+-. 1.6.sup..dagger. 122.8 .+-. 1.7.sup..dagger.,a 107.7 .+-. 2.2*.sup.,.dagger.,a diet IV. 0.5% cholesterol 127.6 .+-. 1.6.sup..dagger. 122.9 .+-. 1.8.sup..dagger.,a 110.0 .+-. 2.6*.sup.,.dagger.,a diet + lignan complex *P < 0.05, 0 month vs 1 and 2 months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs othergroups. .sup.bP < 0.05, Group II vs Group III or Group IV.
TABLE-US-00004 TABLE 4 Hematocrit (L/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 0.327 .+-. 0.00 0.385 .+-. 0.01* 0.376 .+-. 0.01* II. Control diet + 0.357 .+-. 0.00.sup.a 0.382 .+-. 0.01* 0.373 .+-. 0.01 .sup. lignan complex III. 0.5% choles- 0.364 .+-. 0.01.sup.a 0.348 .+-. 0.01*.sup.,a,b 0.300 .+-. 0.01*.sup.,.dagger.,a,b terol diet IV. 0.5% choles- 0.372 .+-. 0.00.sup.a 0.347 .+-. 0.01*.sup.,a,b 0.310 .+-. 0.01*.sup.,.dagger.,a,b terol diet + lignancomplex *P < 0.05, 0 month vs 1 and 2 months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups. .sup.bP < 0.05, Group II vs Group III or Group IV.
TABLE-US-00005 TABLE 5 Mean corpuscular volume (fL) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 64.4 .+-. 0.9 61.8 .+-. 0.9 62.3 .+-. 0.9 .sup. II. Control diet + 62.4 .+-. 1.1 63.4 .+-. 1.0 63.3 .+-. 0.8 .sup. lignan complex III. 0.5% cholesterol 64.2 .+-. 0.4 62.2 .+-. 0.4* 65.3 .+-. 0.5.sup..dagger.,a diet IV. 0.5% cholesterol 63.8 .+-. 0.6 64.0 .+-. 0.6.sup.c 66.1 .+-. 0.6*.sup.,.dagger.,a,b diet + lignan complex *P < 0.05, 0 month vs 1 and 2months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups. .sup.bP < 0.05, Group II vs Group III or Group IV. .sup.cP < 0.05, Group III vs Group IV.
TABLE-US-00006 TABLE 6 Mean Corpuscular Hemoglobin (pg) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 22.0 .+-. 0.34 21.5 .+-. 0.26 21.4 .+-. 0.32 .sup. II. Control diet + 22.1 .+-. 0.38 22.4 .+-. 0.33 21.9 .+-. 0.34 .sup. lignan complex III. 0.5% cholesterol 22.1 .+-. 0.15 22.0 .+-. 0.24 23.4 .+-. 0.20*.sup.,.dagger.,a,b diet IV. 0.5% cholesterol 21.9 .+-. 0.26 22.7 .+-. 0.19*.sup.,a,c 23.4 .+-. 0.23*.sup.,.dagger.,a,b diet + lignan complex *P <0.05, 0 month vs 1 and 2 months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups. .sup.bP < 0.05, Group II vs Group III or Group IV. .sup.cP < 0.05,Group III vs Group IV.
TABLE-US-00007 TABLE 7 Mean Corpuscular Hemoglobin Concentration (g/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 341.8 .+-. 3.8 347.6 .+-. 1.8 343.3 .+-. 1.5 II. Control diet + 354.2 .+-. 1.7 352.5 .+-. 1.7 346.2.+-. 2.4* lignan complex III. 0.5% cholesterol 343.5 .+-. 1.5 351.7 .+-. 2.5 357.7 .+-. 1.9 diet IV. 0.5% cholesterol 342.9 .+-. 2 354.6 .+-. 3.0 354.9 .+-. 1.7 diet + lignan complex *P < 0.05, 0 month vs 1 and 2 months in the respectivegroups.
TABLE-US-00008 TABLE 8 Red Blood Cell Distribution Width (RDW) as % in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 11.68 .+-. 0.22.sup. 12.44 .+-. 0.37 12.84 .+-. 0.35 II. Control diet + 13.52 .+-. 0.28.sup.a 13.1.+-. 0.33 12.95 .+-. 0.32 lignan complex III. 0.5% choles- 11.56 .+-. 0.20.sup.b 12.3 .+-. 0.14*.sup.,b 13.42 .+-. 0.3*.sup.,.dagger. terol diet IV. 0.5% choles- 12.2 .+-. 0.27.sup.b 13.1 .+-. 0.37*.sup.,c 13.17 .+-. 0.21* terol diet + lignancomplex *P < 0.05, 0 month vs 1 and 2 months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups. .sup.bP < 0.05, Group II vs Group III or Group IV. .sup.cP< 0.05, Group III vs Group IV.
TABLE-US-00009 TABLE 9 White Blood Cell Counts (10.sup.9/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 4.96 .+-. 0.62 5.34 .+-. 0.77 5.3 .+-. 0.38 II. Control diet + .sup. 7.7 .+-. 0.7.sup.a 7.33 .+-. 0.25.sup.a4.85 .+-. 0.78*.sup.,.dagger. lignan complex III. 0.5% cholesterol 6.34 .+-. 0.33 8.5 .+-. 0.48*.sup.,a 6.88 .+-. 0.73 diet IV. 0.5% choles- .sup. 6.05 .+-. 0.28.sup.b 9.14 .+-. 0.44*.sup.,a,b 6.59 .+-. 0.93.sup..dagger. terol diet + lignancomplex *P < 0.05, 0 month vs 1 and 2 months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups. .sup.bP < 0.05, Group II vs Group III or Group IV.
TABLE-US-00010 TABLE 10 Granulocytes Content of Blood (10.sup.9/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 0.96 .+-. 0.12 0.64 .+-. 0.08 1.02 .+-. 0.15 II. Control diet + 1.14 .+-. 0.18 1.21 .+-. 0.08* .sup. 0.65 .+-. 0.09.sup..dagger. lignan complex III. 0.5% cholesterol 1.10 .+-. 0.08 1.75 .+-. 0.27*.sup.,a 1.36 .+-. 0.23 diet IV. 0.5% cholesterol 0.87 .+-. 0.078 1.21 .+-. 0.20 1.84 .+-. 0.38* diet + lignan complex *P < 0.05, "0" time vs 1month and 2 months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups.
TABLE-US-00011 TABLE 11 Lymphocyte Counts in Blood (10.sup.9/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 3.42 .+-. 0.44.sup. 4.22 .+-. 0.69 4.0 .+-. 0.29 II. Control diet + 5.27 .+-. 0.33.sup.a 5.53 .+-. 0.27.sup.a 3.87 .+-. 0.65.sup..dagger. lignan complex III. 0.5% cholesterol 4.19 .+-. 0.19.sup.b 6.41 .+-. 0.51* 4.74 .+-. 0.46.sup..dagger.t diet IV. 0.5% cholesterol 4.65 .+-. 0.27.sup.a 5.02 .+-. 0.74 5.09 .+-. 0.56 diet + lignan complex *P< 0.05, 0 month vs 1 and 2 months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups. .sup.bP < 0.05, Group II vs Group III or Group IV.
TABLE-US-00012 TABLE 12 Monocyte Counts in the Blood (10.sup.9/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 0.56 .+-. 0.07 0.46 .+-. 0.05 0.28 .+-. 0.07* II. Control diet + 0.62 .+-. 0.07 0.58 .+-. 0.047 0.33.+-. 0.08*.sup.,.dagger. lignan complex III. 0.5% cholesterol 0.75 .+-. 0.07 0.75 .+-. 0.08.sup.a 0.37 .+-. 0.05*.sup.,.dagger. diet IV. 0.5% cholesterol 0.45 .+-. 0.05.sup.c 0.56 .+-. 0.09 0.45 .+-. 0.02.sup.a diet + lignan complex *P <0.05, "0" month vs 1 month and 2 months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups. .sup.cP < 0.05, Group III or Group IV.
TABLE-US-00013 TABLE 13 Platelet Counts in the Blood (10.sup.9/L) in the Blood of Various Experimental Groups Time (months) Group 0 1 2 I. Control diet 393 .+-. 46.sup. 324 .+-. 52 286 .+-. 25* II. Control diet + 329 .+-. 20.sup. 280 .+-. 8* 267 .+-. 23 lignan complex III. 0.5% cholesterol 422 .+-. 24.sup.b 341 .+-. 26* .sup. 401 .+-. 31.sup.a,b diet IV. 0.5% cholesterol 403 .+-. 20.sup.b 309 .+-. 23* 364 .+-. 37 diet + lignan complex *P < 0.05, "0" month vs other months inthe respective groups. .sup.aP < 0.05, Group I vs other groups. .sup.bP < 0.05, Group II vs Group III or Group IV.
TABLE-US-00014 TABLE 14 Mean Platelet Volume in Fentoliter (fL) for Various Experimental Groups Time (months) Group 0 1 2 I. Control diet 5.38 .+-. 0.27 5.64 .+-. 0.21 5.69 .+-. 0.21 II. Control diet + 6.03 .+-. 0.16 5.81 .+-. 0.11 5.75.+-. 0.11 lignan complex III. 0.5% cholesterol 5.37 .+-. 0.07.sup.a 5.27 .+-. 0.09.sup.a 5.96 .+-. 0.11*.sup.,.dagger. diet IV. 0.5% cholesterol 5.51 .+-. 0.7.sup.a 5.47 .+-. 0.07.sup.a 5.85 .+-. 0.07*.sup.,.dagger. diet + lignan complex *P< 0.05, "0" month vs other months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective groups. .sup.aP < 0.05, Group I vs other groups. .sup.bP < 0.05, Group II vs Group III or Group IV.
TABLE-US-00015 TABLE 15 Serum Alkaline Phosphatase (ALP) Levels (U/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 121.3 .+-. 20.2 152.6 .+-. 10.9 118.1 .+-. 7.7.sup..dagger. II. Control diet + 71.0 .+-. 9.65.sup.alignan complex III. 0.5% cholesterol 169.1 .+-. 16.6 191.5 .+-. 15.6 160.3 .+-. 11.6.sup.a,b diet IV. 0.5% cholesterol 142.7 .+-. 1.4 181.2 .+-. 7.9* 132.7 .+-. 19.5 .sup. diet + lignan complex *P < 0.05, "0" month vs 1 month and 2 months inthe respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups. .sup.bP < 0.05, Group II vs Group III and Group IV.
TABLE-US-00016 TABLE 16 Serum Alanine Aminotransferase (ALT) Levels (U/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 27.25 .+-. 3.6 44.2 .+-. 5.85 41.2 .+-. 3.5* II. Control diet + Not Not 47.33 .+-. 9.2 lignancomplex measured measured III. 0.5% cholesterol 41.22 .+-. 3.1.sup.a 59.3 .+-. 11.2 69.08 .+-. 13.3 diet IV. 0.5% cholesterol 41.6 .+-. 2.6.sup.a 45.4 .+-. 9.4 39.1 .+-. 5.6 diet + lignan complex *P < 0.05, "0" month vs other months in therespective groups. .sup.aP < 0.05, Group I vs other groups.
TABLE-US-00017 TABLE 17 Serum Aspartate Aminotransferase (AST) Levels (U/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 25.0 .+-. 5.1 25.4 .+-. 0.5 41.1 .+-. 3.6*.sup.,.dagger. II. Control diet + Not Not 34.7 .+-. 4.4 lignan complex measured measured III. 0.5% cholesterol 35.0 .+-. 3.3 44.1 .+-. 6.5 53.1 .+-. 2.4*.sup.,a diet IV. 0.5% cholesterol 28.8 .+-. 4.4 29.6 .+-. 2.4 49.4 .+-. 4.5*.sup.,.dagger. diet + lignan complex *P < 0.05, "0" month vs 1month and 2 months in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups.
TABLE-US-00018 TABLE 18 Serum Levels (U/L) of Gamma-glutamyltransferase (GGT) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 9.0 .+-. 0.8 8.8 .+-. 1.0 8.0 .+-. 1.9 II. Control diet + Not Not 8.0 .+-. 1.3 lignan complexmeasured measured III. 0.5% cholesterol 9.6 .+-. 0.4 8.6 .+-. 0.8 6.4 .+-. 1.7 diet IV. 0.5% cholesterol 9.0 .+-. 1.1 6.5 .+-. 0.6 6.4 .+-. 1.2 diet + lignan complex
TABLE-US-00019 TABLE 19 Serum Albumin Levels (gm/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 15.8 .+-. 0.2 17.8 .+-. 0.37* 30.3 .+-. 5.2 II. Control diet + 35.50 .+-. 4.52 lignan complex III. 0.5% cholesterol16.9 .+-. 0.31 18.3 .+-. 0.42* 20.41 .+-. 2.58 diet IV. 0.5% cholesterol 17.2 .+-. 0.2 19.0 .+-. 0.54* 26.77 .+-. 4.1 diet + lignan complex *P < 0.05, comparison of the values at various times with respect to "0" time in the respective groups.
TABLE-US-00020 TABLE 20 Serum Creatinine Levels (.mu.moles/L) in the Experimental Groups Time (months) Group 0 1 2 I. Control diet 48.4 .+-. 2.46 78.8 .+-. 2.35* 103.3 .+-. 5.4*.sup.,.dagger. II. Control diet + Not Not 104.25 .+-. 6.2*lignan complex measured measured III. 0.5% cholesterol 62.12 .+-. 1.68.sup.a 80.7 .+-. 3.9* 106.4 .+-. 4.6*.sup.,.dagger. diet IV. 0.5% cholesterol 60.0 .+-. 6.0 73.2 .+-. 3.7 97.56 .+-. 5.33*.sup.,.dagger. diet + lignan complex *P < 0.05,comparison of values at various times with respect to "0" time in the respective groups. .sup..dagger.P < 0.05, 1 month vs 2 months in the respective group. .sup.aP < 0.05, Group I vs other groups.
Since lignan complex lowers serum cholesterol, elevates serum HDL-C and reduces hypercholesterolemic atherosclerosis it will be of use in the prevention and treatment of the following diseases: i) Hypercholesterolemic atherosclerosis. ii)Coronary artery disease (heart attack). iii) Stroke. iv) Restenosis following percutaneous transluminal coronary angioplasty. v) Restenosis after stent implant. vi) Stroke, heart attack, renal failure and retinopathy in diabetes mellitus. vii)Hypercholesterolemia. viii) Peripheral vascular diseases, such as intermittent clandication.
The use of lignan complex derived from flaxseed according to this invention has the following advantages: i) Lignan complex contains materials that have antioxidant and anti-PAF activity and hence is an anti-inflammatory agent. ii) It lowersserum cholesterol, raises HDL-C and reduces hypercholesterolemic atherosclerosis. iii) This compound is a natural food product and has no toxicity on hemopoietic system, liver and kidney, and it is a safe drug. iv) It is inexpensive and safe ascompared to other drugs used for lowering lipids and reducing atherosclerosis. v) This compound is cheaper than SDG because processing of SDG is expensive as compared to lignan complex. vi) The dose of lignan complex is very small as compared toflaxseed.
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