- Research article
- Open Access
Comparison of plasma lipoprotein profiles and malondialdehyde between hyperlipidemia dogs with/without treatment
© Li et al.; licensee BioMed Central Ltd. 2014
Received: 18 September 2013
Accepted: 5 March 2014
Published: 14 March 2014
The aim of this study is to compare metabolic parameters, malondialdehyde as a lipid oxidation marker, and lipid profiles between dogs with untreated hyperlipidemia and hyperlipidemia with treatment, in order to examine the usefulness of malondialdehyde and lipid profiles as diagnostic parameters at early stages of hyperlipidemia.
Dog samples were collected from four different veterinary clinics across Japan from March to June 2013. They were separated into three groups: control, untreated hyperlipidemia based on temporally screening, and hyperlipidemia with current anti-hyperlipidemic (statins and fibrates) treatment. Triglyceride levels of untreated hyperlipidemia dogs were significantly higher than those of control dogs. ALT levels of hyperlipidemic dogs with treatment were the highest among three groups. VLDL and LDL of both cholesterol and triglyceride of untreated hyperlipidemia dogs were the highest among three groups. HDL1 levels in triglyceride of hyperlipidemia dogs with treatment were significantly higher than those of control and untreated hyperlipidemia dog. Malondialdehyde concentrations of untreated hyperlipidemia dogs were significantly higher than those of control and hyperlipidemic dogs with treatment.
In this study, dogs with untreated hyperlipidemia clearly showed abnormal lipid status, whereas hyperlipidemic dogs under anti-hyperlipidemia treatment showed more normal lipid status suggesting the effectiveness of the therapy. Anti-hyperlipidemics (statins and fibrates) for dogs are also effective in relieving elevated levels of lipids and lipid oxidation. Plasma lipid (triglyceride and cholesterol) profiles and malondialdehyde are useful diagnostic tools for identifying early stages of untreatment hyperlipidemia in dogs.
Aberrations in plasma cholesterol and triglyceride levels are indicative of diseases associated with obesity and diabetes mellitus . Mounting evidences have suggested the increasing recognition of clinical importance of hyperlipidemia in dogs. Hyperlipidemia causes other disorders such as pancreatitis, hypotiroidism [2, 3]. However, many of hyperlipidemia dogs physically appear healthy and do not usually exhibit any symptoms. Therefore, many veterinary practitioners and dog owners exhibit little interest in unsymptomatic lipid metabolism abnormality. Only when the disease progresses and the dog become severely hyperlipidemic, they initiate therapy with anti-hyperlipidemic drugs. In 2012, we set the new screening criteria for detecting early stages of hyperlipidemia in dogs . When we evaluated apparently healthy dogs using these criteria, 23.7% dogs (9 of healthy 38 dogs) were diagnosed with hyperlipidemia. We think that the use of hyperlipidemia screening is valuable in early diagnosis, which in turn, allows for an implementation of early interventions such as diet change, exercise, and more frequent veterinary check-ups. In humans, plasma lipid profile analysis can be useful in diagnosing lipid metabolic disorders. Lipoproteins are believed to play important roles in energy and lipid metabolism of animals, and can reflect metabolic changes. Alterations in the dog’s lipoprotein cholesterol fractions are possibility of aberrations of lipid metabolism due to hyperlipidemia and/or obesity as in human .
Hyperlipidemia also induces oxidative stress, and malondialdehyde (MDA) is one of the end products in lipid peroxidation. Plasma MDA levels increased markedly in animals with obesity and diabetes mellitus and increased MDA indicated elevations of lipid oxidation in tissues . Humans with apparent increase in Malondialdehyde-Modified LDL were shown to be more predisposed to developing arterosclerosis. However it should be noted, dog’s lipoprotein density profiles and lipid metabolism are different from those of humans [5, 7].
The aim of this study is twofold. First is to reveal how the effect of the anti-hyper lipidemic therapy on lipid profiles of hyperlipidemia dogs. There are 2 types of hyperlipedemia dogs; Fisrt hyperlipidemia dog group is classified as untreated hyperlipedemia, and another group of hyperlipidemia dogs managed with lipid-lowering drugs was classified as hyperlipidemia with current treatment.
Second is to compare metabolic parameters, MDA as a lipid oxidation marker, and lipid profiles between dogs with untreated hyperlipidemia, and hyperlipidemia with treatment in order to examine the usefulness of MDA and lipid profiles as diagnostic parameters at early stages of hyperlipidemia.
Elevated triglyceride level >165 mg/dL
Elevated total cholesterol level >200 mg/dL
Elevated free fatty acids level >1.5 mEq/L
All dog owners gave us written informed consent before enrolment in this study. This study was approved by the Nippon Veterinary and Life Science University Animal Research Committee.
Blood sampling and plasma metabolite analysis
Postprandial blood samples were collected from the forelimb vein into heparinized plastic tubes, and plasma was recovered via centrifugation at 4°C and stored at -25°C until further use. Plasma glucose, triglycerides (TG), total cholesterol (T-cho), total protein, aspartate aminotransferase, and alanine aminotransferase (ALT), alkaline phosphatase (ALP), albumin, albumin verses globulin ratio, total bilirubin, total bile acids, γ-GTP were measured by auto-analyzer (Monolis, Inc, Tokyo, Japan) using the manufacturer’s reagents. NEFA, adiponectin, insulin and MDA were determined with NEFA-C test Wako (Wako Pure Chemical Industries, Inc., Tokyo), Dog adiponectin ELISA kit (Circulex Co., Ltd, Nagano), and Lbis dog Insulin kit (Shibayagi Co., Gunma), Malondialdehyde Assay kit, (Northwest Life Science Specialties LLC, Vancouver, WA) respectively.
In order to examine lipoprotein fractions of cholesterol and triglyceride for all dogs, we performed biphasic agarose gel electrophoresis method using commercial Quickgel Lipo gels (Helena Laboratories, Saitama). Lipoproteins were separated by electrophoretic technique and analyzed using a Helena Laboratories Epalyzer 2 Electrophoresis processing Analyzer. Lipoprotein fractions were assessed and analyzed using Edbank III analysis software (Helena Laboratories, Saitama, Japan). Lipoprotein electrophoresis pattern consisted of 4 bands. The bands from left to right were: α1-migrating lipoproteins (HDL2 and HDL3), α2-migrating lipoproteins (HDL1), β-migrating lipoproteins (LDL and VLDL), and κ band (small% of chylomicrons) remaining at the origin (Mori et al., ).
Values were expressed in medians with inter-quartile range (25th Percentile and 75th Percentile). Statistical significance was determined by One-way Ananysis of Variance by Ranks among groups. All tests were performed using Sigmaplot version.11.2 (Systat Software Inc., San Diego, CA, USA). The significance level was set at P < 0.05.
Comparison of plasma biomarker levels and lipoprotein profiles among control, hyperlipidemia dogs with/without treatment
With treatment (4)
Body condition score
Body weight (kg)
Total choresterol (mg/dL)
Total protein (g/dL)
Total bilirubin (mg/dL)
Total bile acid (mg/dL)
Various diagnostic criteria for hyperlipidemia have already been established. The first states plasma total cholesterol level of over 300 mg/dl as a criterion , and another sets both plasma triglyceride and plasma cholesterol levels to be over 500 mg/dl . The above methods only detect dogs which are in severe hyperlipidemic condition and in need of clinical interventions. Our screening methods aim to detect early stages of hyperlipidemia in dogs that may be missed by veterinarinary practitioners. In current study, abnormal lipid satus in plasma was clearly detected in untreated hyperlipidemia group. In this study, most of the hyperlipidemic dogs were under anti-hyperlipidemic therapy as recommended by their veterinarians. The therapy appeared to be fully effective since triglyceride level in hyperlipidemia with treatment group was lower than those of untreated hyperlipidemia group and there was no significant difference in plasma cholesterol levels among three groups. At the time of the blood draw, three of four hyperlipidemic dogs were on fibrates and one dog was on statins. The fibrates are considered the most effective hypertriglyceridemia drugs  and the statins are a class of LDL-cholesterol lowering drugs [11, 12]. ALT levels in hyperlipidemic dogs with treatment were expected to be elevated due to hepatic metabolism of these drugs. HDL1 is a large floating particle which plays an important role in reverse cholesterol transport. LDL functions similarly as HDL 1, and is unique to dogs . HDL1 fractions of both cholesterol and triglycerides in hyperlipidemia with treatment group were the highest among three groups. Additionally, we confirmed correlations between MDA and lipid profiles for each group. MDA level of normal group showed strongly positive correlations with triglycerides level, VLDL of triglycerides (TG r = 0.89, VLDL of TG r = 0.82). Remarkably, MDA level of untreated hyperlipidemia group showed strongly positive correlations with a lot of lipid profiles (T-Cho r = 0.83, HDL2 and HDL3 of T-cho r = 0.86, HDL1 of T-cho r = 0.72, VLDL and LDL of T-cho r = 0.97, HDL1 of TG r = 0.78, VLDL and LDL of TG r = 0.79). Adversely MDA of hyperlipidemia with treatment correlated negatively with total cholesterol level (T-cho, r = -0.75). The highest value of coefficient of correlation was seen between MDA and VLDL/LDL of total cholesterol.
Anti-hyperlipidemic drugs were also effective in reducing lipid oxidation. MDA concentration in untreated hyperlipidemic dogs was the highest among three groups. MDA is an end product of lipid peroxidation, and MDA-modified LDL (MDA-LDL) is generated via lipid peroxidation or during platelet aggregation. Both statins and fibrates therapies had a positive effect on reducing serum MDA-LDL concentrations in human lipid metabolic mechanism [13, 14]. Also statins and fibrates in dogs are effective in relieving the increased lipids and lipid oxidation. Untreated hyperlipidemia group showed significantly higher plasma triglycerides concentration than control and hyperlipidemia with treatment groups. Associated VLDL and LDL in lipoprotein fractions were also higher than those of control and hyperlipidemia with treatment groups. As untreated hyperlipidemia dogs showed abnormality in lipid metabolism, our new criteria in hyperlipidemia is shown to be beneficial in metabolic disease prevention. Xenoulis et al.  also reported in current paper that lipoprotein profiles in dogs could potentially be useful as diagnostic tools in idenfication of dogs suspected of having lipoprotein abnormalities.
Unfortunately, in this study, there was an insufficient number of with/ without treatment hyperlipidemic dogs. The small number of dogs may result in low statistical power, hence results and conclusions need to be interpreted with care. However, this study showed that changes in lipid metabolism are reflected in liver. In the future, we hope to add more sample numbers and to repeat our study using different stages of hyperlipidemia dogs and establish base values of lipid profiles and MDA concentrations as new markers in hypelipidemia screening in order to validate our results.
In this study, dogs with untreated hyperlipidemia clearly showed abnormal lipid status, whereas hyperlipidemic dogs under anti-hyperlipidemia treatment showed more normal lipid status suggesting the effectiveness of the therapy. Plasma lipid (triglycerides and cholesterol) profiles and MDA may be useful as diagnostic tools for early stages of hyperlipidemia dogs.
The authors would like to thank Kodomonokuni Animal hospital (Kanagawa), Togashira Animal hospital (Ibaraki), Sagamihara purimo Animal hospital (Kanagawa), Morinoinuneko Animal Hospital (Kanagawa) in obtaining dog’s blood samples.
- Bauer JE: Lipoprotein-mediated transport of dietary and synthesized lipids and lipid abnormalities of dogs and cats. J Am Vet Med Assoc. 2004, 224: 668-675. 10.2460/javma.2004.224.668.View ArticlePubMedGoogle Scholar
- Fleeman L: Is hyperlipidemia clinically important in dogs?. Vet J. 2010, 183: 10-10.1016/j.tvjl.2008.12.008.View ArticlePubMedGoogle Scholar
- Xenoulis PG, Steiner JM: Lipid metabolism and hyperlipidemia in dogs. Vet J. 2010, 183: 12-21. 10.1016/j.tvjl.2008.10.011.View ArticlePubMedGoogle Scholar
- Kawasumi K, Suzuki T, Fujiwara M, Mori N, Yamamoto I, Arai T: New criteria of hyperlipidemia with insulin resistance in dogs. J Anim Vet Adv. 2012, 11: 3950-3952.Google Scholar
- Mori N, Lee P, Kondo K, Kido T, Saito T, Arai T: Potential use of cholesterol lipoprotein profile to confirm obesity status in dogs. Vet Res Commun. 2011, 35: 223-235. 10.1007/s11259-011-9466-x.View ArticlePubMedGoogle Scholar
- Moussa SA: Oxidative stress in diabetes mellitus. Rom J Biophys. 2008, 18: 225-236.Google Scholar
- Terpstra AH, Sanchez-Muniz FJ, West CE, Woodward CJ: The density profile and cholesterol concentration of serum lipoproteins in domestic and laboratory animals. Comp Biochem Physiol B. 1982, 71: 669-673.PubMedGoogle Scholar
- Whitney MS: Evaluation of hyperlipidemias in dogs and cats. Semin Vet Med Surg (Small Anim). 1992, 7: 292-300.Google Scholar
- Mori N, Lee P, Muranaka S, Sagara F, Takemitsu H, Nishiyama Y, Yamamoto I, Yagishita M, Arai T: Predisposition for primary hyperlipidemia in miniature schnauzers and Shetland sheepdogs as compared to other canine breeds. Res Vet Sci. 2010, 88: 394-399. 10.1016/j.rvsc.2009.12.003.View ArticlePubMedGoogle Scholar
- Brunzell JD, Bierman EL: Chylomicronemia syndrome. Interaction of genetic and acquired hypertriglyceridemia. Med Clin North Am. 1982, 66: 455-468.PubMedGoogle Scholar
- Bilheimer DW, Grundy SM, Brown MS, Goldstein JL: Mevinolin stimulates receptor-mediated clearance of low density lipoprotein from plasma in familial hypercholesterolemia heterozygotes. Trans Assoc Am Physicians. 1983, 96: 1-9.PubMedGoogle Scholar
- Tamura A, Watanabe T, Nasu M: Effects of atorvastatin and pravastatin on malondialdehyde-modified LDL in hypercholesterolemic patients. Circ J. 2003, 10: 816-820.View ArticleGoogle Scholar
- Kondo A, Manabe M, Saito K, Maekawa M, Kanno T: Insulin treatment prevents LDL from accelerated oxidation in patients with diabetes. J Atheroscler Thromb. 2002, 9: 280-7. 10.5551/jat.9.280.View ArticlePubMedGoogle Scholar
- Kanno T, Maekawa M: Influence of fibrate treatment on malondialdehyde-modified LDL concentration. Clin Chim Acta. 2004, 339: 97-103. 10.1016/j.cccn.2003.09.005.View ArticlePubMedGoogle Scholar
- Xenoulis PG, Cammarata PJ, Walzem RL, Macfarlane RD, Suchodolski JS, Steiner JM: Novel lipoprotein density profiling in healthy dogs of various breeds, healthy miniature schnauzers, and miniature schnauzers with hyperlipidemia. BMC Vet Res. 2013, 9: 47-10.1186/1746-6148-9-47.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.