- Open Access
Sex hormones affect endothelial lipase-mediated lipid metabolism and atherosclerosis
Lipids in Health and Disease volume 18, Article number: 226 (2019)
Endothelial lipase (EL) plays an important role in lipoprotein metabolism and atherosclerosis. To study the functional roles of EL, we recently generated transgenic (Tg) rabbits and reported that increased hepatic expression of EL in male Tg rabbits significantly reduced diet-induced hypercholesterolemia compared with non-Tg controls. This gender difference suggests that sex hormones may mediate EL functions thereby influencing lipoprotein metabolism. To examine this hypothesis, we compared the effects of orchiectomy and ovariectomy on plasma lipids and diet-induced atherosclerosis in both Tg and non-Tg rabbits.
Male rabbits were under orchiectomy whereas female rabbits were under ovariectomy. We compared plasma lipids, lipoproteins, and apolipoproteins of rabbits before and after surgery in each group fed either a chow diet or cholesterol-rich diet.
On a chow diet, both male and female Tg rabbits showed lower plasma lipids than non-Tg counterparts and this lipid-lowering effect of EL was not affected by either orchiectomy in male or ovariectomy in female Tg rabbits. On a cholesterol diet; however, male Tg rabbits but not female Tg rabbits showed significant resistance to diet-induced hypercholesterolemia and atherosclerosis. The EL-mediated atheroprotective effect was eliminated after orchiectomy in male Tg rabbits. Female Tg rabbits showed similar levels of total cholesterol and lesion size of atherosclerosis compared with non-Tg rabbits and ovariectomy did not affect diet-induced hypercholesterolemia or atherosclerosis.
These results suggest that increased EL protects against diet-induced hypercholesterolemia and atherosclerosis. The beneficial effect of EL was dependent upon the presence of androgenic hormones.
Atherosclerotic complications such as myocardial infarction and stroke are the major cause of morbidity and mortality in the world [1, 2]. Atherosclerosis is related with a number of genetic and environmental factors and its pathogenesis is associated with many risk factors, such as hyperlipidemia, hypertension, diabetes and smoking [3,4,5,6]. In addition, many other factors are also involved in the development of atherosclerosis. For example, it is well known that the prevalence of atherosclerosis is lower in women before menopause than men. Epidemiological, clinical, and experimental studies have provided ample evidence that there are gender-specific variations in cardiovascular risks [7,8,9,10]. However, after menopause, the risk of atherosclerosis in women begins to rise and even exceed that in men, suggesting that estrogen exerts athero-protective functions through mediation of vascular functions and lipoprotein metabolism, hemostasis and fibrinolysis [11,12,13,14,15,16,17]. In spite of this, gender-differences cannot be completely explained by estrogen alone and interactions between sex hormones and other factors also play a role in atherosclerosis although it is not completely understood regarding these factors.
Sex hormones affect may many facets of lipid metabolism through interactions with other regulators. Apolipoprotein E (apoE) and lipoprotein lipase (LPL), two important mediators in lipoprotein metabolism, are significantly affected by sex hormones because male and female animals exhibit different lipoprotein profiles and response to a cholesterol diet and atherosclerosis when these two genes are overexpressed [18, 19]. Endothelial lipase (EL) was originally cloned from endothelial cells [20, 21], but EL is also expressed in liver, lung, thyroid, and kidney [22, 23]. Although EL, LPL, and hepatic lipase (HL) hydrolyze both triglycerides (TG) and phospholipids (PL) in the lipoproteins, they show different substrate selectivity. EL exhibits high phospholipase activity in high-density lipoproteins (HDL) but low triglyceride lipase activity, whereas LPL and HL mainly exercise TG lipase activity [24, 25]. Previous studies have shown that EL mediates HDL-cholesterol (HDL-C) levels along with VLDL levels [21, 26]. Recently, we found that expression of hepatic EL showed a significant influence on plasma lipids and lipoprotein metabolism . Interestingly, increased hepatic expression of EL inhibits cholesterol diet–induced hypercholesterolemia and protects against atherosclerosis in male Tg rabbits but not in female Tg rabbits. This finding prompted us to envision that there is an interaction between EL and sex hormones thereby influencing lipoprotein metabolism and atherosclerosis. To investigate this issue, we compared the lipoprotein features in male and female rabbits after castration. Our current study showed that gender differences in lipid metabolism and atherosclerosis observed in EL Tg rabbits are dependent on the presence of androgens but not estrogens.
Materials and methods
Transgenic (Tg) Japanese white rabbits expressing the human EL in the liver were generated in our laboratory as described previously . Rabbits were fed with a chow diet (RM-4, Funabashi Farmer) containing 16.5% protein, 4.2% fat, and 13% crude fiber. Tg rabbits along with sex- and age-matched non-Tg littermates (4–6 months old) were used for the current study. For a cholesterol diet experiments, all rabbits were fed with a chow diet supplemented with 0.3% cholesterol and 3% soybean oil for 16 weeks. AII animal experiments were performed with the approval of the Animal Care Committee of the University of Yamanashi and Saga and conformed to the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health.
Analysis of plasma lipids and lipoproteins
Plasma levels of total cholesterol (TC), triglycerides (TG) and HDL cholesterol (HDL-C) were measured using enzymatic assay kits (Wako Pure Chemical Industries Ltd., Osaka) [27, 28]. Plasma lipoproteins were further isolated by sequential gradient ultracentrifugation and then subjected to a 1% agarose gel (Helena Laboratories, Saitama, Japan) electrophoresis and stained with Fat Red 7B or transferred to a nitrocellulose membrane for immunoblotting with polyclonal antibodies (Abs) against apoB, apoE (Rockland Inc., Limerick, PA, USA), and apoAI (Bio-Rad AbD Serotec, Kidlington, UK). Lipoprotein fractions were fractionated by 4~20% SDS-PAGE. Apolipoproteins were visualized by Coomassie brilliant blue (CBB) staining. TC and TG contents in each density fraction were measured using the Wako assay kits described above [27, 28].
Effects of sex hormone on lipids and atherosclerosis
To investigate the effect of sex hormones on EL-mediated lipoprotein metabolism, male Tg rabbits along with non-Tg littermates were undergone a bilateral orchiectomy whereas female Tg rabbits and littermates were undergone a bilateral ovariectomy . All castrated rabbits were further fed a cholesterol-rich diet containing 0.3% cholesterol and 3% soybean oil for 16 weeks and then their plasma lipids and aortic lesions of atherosclerosis were compared. Because only male Tg rabbits showed protection against diet-induced hypercholesterolemia (see below), we envisioned that estrogen may suppress the functions of EL in male rabbits. To investigate this issue, male Tg rabbits and non-Tg littermates at 4 months of age were intramuscularly injected with 17α-ethinyl estradiol (Sigma-Aldrich, St. Louis; USA) at a dose of 100 μg/kg/day for 10 days . After estrogen injection or ovariectomy, blood was collected from fasted rabbits for plasma lipid analysis as described above. Plasma levels of testosterone and estradiol were measured using Electro chemiluminescence immunoassay (ECLIA) (SRL, Inc. Tokyo, Japan). Plasma EL levels were measured using an ELISA kit as described previously .
Quantification of aortic atherosclerosis
At the end of cholesterol diet feeding for 16 weeks, all rabbits were euthanized by injection of an overdose of sodium pentobarbital solution. The whole aortas were stained with Sudan IV for evaluation of the gross lesion size as described previously . For microscopic evaluation of the lesion area, the aortic arch was dissected into 10 sections and embedded in paraffin. Serial sections (3 μm thick) were stained with hematoxylin-eosin (HE), elastica van Gieson (EVG) and immunohistochemically stained with monoclonal Abs against macrophages RAM11 (Dako Inc., Carpinteria, CA) (1:400 dilution) and smooth muscle α-actin HHF35 (Dako Inc., Carpinteria, CA) (1200 dilution). The microscopic lesion area, macrophage and SMC contents in the lesions were quantified with WinRoof image analysis system (Mitani Co., Tokyo, Japan) .
All data are expressed as mean ± SD. ANOVA was used for lipid parameter analysis and Mann-Whitney U-test was used for lesion analysis using SPSS 22.0 software. P values < 0.05 were considered significant.
Plasma lipids and lipoproteins
On a chow diet, both male and female Tg rabbits showed significant reduction of plasma total cholesterol mainly caused by significant decrease of HDL-C levels (Fig. 1). Plasma levels of TC were reduced by 68% in males and 47% in females while HDL-C levels were reduced by 90% in males and 65% in females compared with non-Tg counterparts. Plasma TG levels were not significantly changed in Tg males and females compared with non-Tg rabbits.
On a cholesterol diet for 16 weeks; however, male Tg rabbits exhibited protection against diet-induced hypercholesterolemia: TC, TG and HDL-C levels of Tg rabbits remained lower than those of non-Tg rabbits (Fig. 1). In contrast, in female Tg rabbits, TC, TG and HDL-C levels were not significantly different from those of non-Tg groups after a cholesterol diet feeding (Fig. 1).
In the previous study, we showed that there was a marked change in male Tg rabbits compared with non-Tg rabbits: there was a remarkable reduction of apoB-containing particles associated with reduced contents of apoB and apoE as shown in the previous studies .
However, female Tg rabbits showed a similar lipoprotein profile including apoB and apoE contents in apoB-containing particles and apoAI and apoE in HDL particles compared with non-Tg females (Fig. 2a–b). Quantitation of TC and TG contents in these fractions showed that all lipoproteins were similar in female Tg rabbits compared with non-Tg females (Fig. 2c).
These observations suggest that sex hormones may affect the functions of EL in Tg rabbits on a cholesterol diet.
Effects of castration on plasma lipids and atherosclerosis
To determine if ablation of endogenous androgen or estrogen would affect EL-mediated lipoprotein metabolism and atherosclerosis, we examined the changes of male rabbits that were undergone a bilateral orchiectomy and female rabbits that were undergone a bilateral ovariectomy. Orchiectomy dropped the plasma levels of testosterone (1.15 ng ± 0.44 ng/ml to 0.25 ± 0.06 nm/ml after orchiectomy, n = 6 for each group) and elevated plasma EL in male Tg rabbits on a chow diet (Additional file 1: Figure S1). Ovariectomy did not change the plasma levels of EL in female Tg rabbits on a chow diet but elevated EL when they were on a cholesterol-rich diet. Regardless of this, as shown in Fig. 3, castration did not affect the plasma lipids in both male and female rabbits on a chow diet. Plasma levels of TC and HDL-C remained at lower in Tg rabbits compared with non-Tg counterparts. We were particularly interested in male Tg rabbits because they showed protection against diet-induced hypercholesterolemia (Fig. 1). We further intramuscularly injected male rabbits with 17α-ethinyl estradiol for 10 days. Similar to orchiectomied male rabbits, estrogen injection in male rabbits did not change the patterns of plasma lipids compared with un-injected rabbits (Fig. 4). These results suggest that sex hormones did not directly influence EL-mediated lipid metabolism in Tg rabbits on a chow diet.
Then, we fed castrated rabbits with a cholesterol-rich diet for 16 weeks and compared their plasma lipids with uncastrated controls. Interestingly, castrated Tg male rabbits showed similar “high” hypercholesterolemia compared with non-Tg rabbits: TC, TG and HDL-C levels were basically similar to those of non-Tg rabbits (Fig. 5). In another word, EL-mediated protection against hypercholesterolemia in male Tg rabbits was totally eliminated by castration. On the contrary, castrated female Tg rabbits had similar levels of lipids compared to non-Tg rabbits, as those uncastrated female rabbits: there was no significant difference in plasma lipids of Tg rabbits and non-Tg rabbits regardless of castration (Fig. 5).
Finally, we analyzed en face aortic lesion areas and found that the whole aortic atherosclerotic lesions of male Tg rabbits were significantly reduced by 61% in the total aorta compared with non-Tg rabbits. However, after castration, male Tg rabbits showed similar lesion size to that of non-Tg rabbits. This result suggests that castration eliminated atheroprotective effects of EL in male Tg rabbits because there was no significant difference in both plasma TC and aortic atherosclerosis between castrated Tg rabbits and non-Tg rabbits (Fig. 6a). In female rabbits; however, Tg showed similar atherosclerosis lesion area compared with non-Tg rabbits both in uncastrated and castrated rabbits (Fig. 6b). Microscopically, the lesions of atherosclerosis were not significantly changed including the lesion size and cellular components after castration (data not shown).
In the current study, we attempted to elucidate whether sex hormones affect EL-mediated lipoprotein metabolism and atherosclerosis in rabbits fed both chow and cholesterol diets. This study was performed based on the previous observation that increased EL expression in male Tg rabbits protected against cholesterol-induced hypercholesterolemia and atherosclerosis . We found that lipoprotein changes were more prominent in male Tg than female Tg rabbits even on a chow diet. In addition, male but not female Tg rabbits showed protection against cholesterol diet induced hypercholesterolemia and aortic atherosclerosis. This gender difference in terms of EL functions was initially surprising but also reported in EL KO mice. Ishida et al. reported that LDL-C levels were increased by 90% in male LIPG−/− mice as compared with wild-type mice, but no change in females . They showed a significant 24% decrease in the lesion area of male LIPG−/−/apoE−/− mice when compared with apoE−/− mice; however, the difference was smaller and not statistically significant between female LIPG−/−/apoE−/− and apoE−/− mice .
As we reported in the previous studies, male Tg rabbits showed constantly and significantly lower levels of TC and HDL-C on both chow and cholesterol-rich diets . In HDLs, phospholipids contents were remarkably reduced in both male and female Tg rabbits . In contrast, female Tg rabbits showed lower levels of plasma TC and HDL-C but only on a chow diet. When female Tg rabbits were challenged with a cholesterol diet, they developed similar “high” hypercholesterolemia as non-Tg rabbits. Therefore, EL-mediated cholesterol-lowering and atheroprotective effects were only present in male Tg rabbits, raising a possibility that sex hormones may be involved in EL-lipoprotein metabolism especially on a cholesterol diet.
We initially hypothesized that either estrogen inhibits EL functions or androgen enhances EL functions. To answer these two questions, we performed orchiectomy in males and ovariectomy in females. Our current studies showed that it is mostly likely that the presence of androgen in male Tg rabbits is required for the lipid-lowering and atheroprotective effects of EL because orchiectomy can completely eliminate these beneficial effects of EL. On the other hand, estrogen, if any, has very little influence on EL functions because ovariectomy in females or estrogen treatment in males did not change the lipoprotein profiles and diet-induced hypercholesterolemia and atherosclerosis. In spite of this observation, it is currently unknown how androgen interacts with EL and further studies are needed to elucidate molecular mechanisms. In our previous study, we did not find any difference of EL concentrations of post-heparin plasma between male and female Tg rabbits, suggesting that androgen or estrogen does not directly mediate EL expression . We have found that lipid-lowering functions of EL are essential for atheroprotective effects in male Tg rabbits (Niimi et al. submitted for publication). In light of these findings, there is another possibility that androgen may help promote the hepatic catabolism of apoB-containing particles in male Tg rabbits because we recently showed that Dil-labeled β-VLDL clearance was faster in Tg rabbits than non-Tg rabbits. How androgen interacts with EL; however, requires future investigations. There is a need to delineate the underlying molecular mechanisms of androgen-EL-lipoprotein metabolism. It is well known that sex hormones mediate lipid metabolism and cholesterol biology through a number of pathways [4, 18, 30,31,32]. Although it is generally believed that androgen such as testosterone may increase men’s cardiovascular risk, it is not clear whether androgen has some other beneficial effects on lipoprotein metabolism in humans. In support of speculation, it has been reported that men with lower testosterone levels tend to have higher incidence of coronary artery disease [33, 34].
In conclusion, our study has shown that increased expression of EL inhibits diet-induced hypercholesterolemia and atherosclerosis in a gender-dependent manner. Although the molecular mechanisms remain to be defined, it seems that androgen is involved in the lipid-lowering and atheroprotective effects of EL in Tg rabbits.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author upon request.
Very low-density lipoprotein
Roth GA, Johnson C, Abajobir A, Abd-Allah F, Abera SF, Abyu G, Ahmed M, Aksut B, Alam T, Alam K, et al. Global, regional, and national burden of cardiovascular diseases for 10 causes, 1990 to 2015. J Am Coll Cardiol. 2017;70:1–25.
Fowkes FG, Rudan D, Rudan I, Aboyans V, Denenberg JO, McDermott MM, Norman PE, Sampson UK, Williams LJ, Mensah GA, Criqui MH. Comparison of global estimates of prevalence and risk factors for peripheral artery disease in 2000 and 2010: a systematic review and analysis. Lancet. 2013;382:1329–40.
Nelson RH. Hyperlipidemia as a risk factor for cardiovascular disease. Prim Care. 2013;40:195–211.
Anderson KM, Castelli WP, Levy D. Cholesterol and mortality. 30 years of follow-up from the Framingham study. JAMA. 1987;257:2176–80.
Assmann G, Schulte H. The Prospective Cardiovascular Munster (PROCAM) study: prevalence of hyperlipidemia in persons with hypertension and/or diabetes mellitus and the relationship to coronary heart disease. Am Heart J. 1988;116:1713–24.
Burke GM, Genuardi M, Shappell H, D'Agostino RB Sr, Magnani JW. Temporal Associations Between Smoking and Cardiovascular Disease, 1971 To 2006 (from the Framingham heart study). Am J Cardiol. 2017;120:1787–91.
Cifkova R, Krajcoviechova A. Dyslipidemia and cardiovascular disease in women. Curr Cardiol Rep. 2015;17:609.
Zhang XE, Cheng B, Wang Q, Wan JJ. Association of gender-specific risk factors in metabolic and cardiovascular diseases: an NHANES-based cross-sectional study. J Investig Med. 2018;66:22–31.
Wild S, Pierpoint T, McKeigue P, Jacobs H. Cardiovascular disease in women with polycystic ovary syndrome at long-term follow-up: a retrospective cohort study. Clin Endocrinol. 2000;52:595–600.
Vitale C, Fini M, Speziale G, Chierchia S. Gender differences in the cardiovascular effects of sex hormones. Fundam Clin Pharmacol. 2010;24:675–85.
Kannel WB, Hjortland MC, McNamara PM, Gordon T. Menopause and risk of cardiovascular disease: the Framingham study. Ann Intern Med. 1976;85:447–52.
Abbott RD, Garrison RJ, Wilson PW, Epstein FH, Castelli WP, Feinleib M, LaRue C. Joint distribution of lipoprotein cholesterol classes. The Framingham study. Arteriosclerosis. 1983;3:260–72.
Mathur P, Ostadal B, Romeo F, Mehta JL. Gender-related differences in atherosclerosis. Cardiovasc Drugs Ther. 2015;29:319–27.
Nguyen TT, Hernandez Mijares A, Johnson CM, Jensen MD. Postprandial leg and splanchnic fatty acid metabolism in nonobese men and women. Am J Phys. 1996;271:E965–72.
Gardner CD, Tribble DL, Young DR, Ahn D, Fortmann SP. Population frequency distributions of HDL, HDL (2), and HDL (3) cholesterol and apolipoproteins A-I and B in healthy men and women and associations with age, gender, hormonal status, and sex hormone use: the Stanford five city project. Prev Med. 2000;31:335–45.
Schaefer EJ, Lamon-Fava S, Cohn SD, Schaefer MM, Ordovas JM, Castelli WP, Wilson PW. Effects of age, gender, and menopausal status on plasma low density lipoprotein cholesterol and apolipoprotein B levels in the Framingham offspring study. J Lipid Res. 1994;35:779–92.
Jenner JL, Ordovas JM, Lamon-Fava S, Schaefer MM, Wilson PW, Castelli WP, Schaefer EJ. Effects of age, sex, and menopausal status on plasma lipoprotein(a) levels. The Framingham Offspring Study. Circulation. 1993;87:1135–41.
Huang Y, Schwendner SW, Rall SC Jr, Sanan DA, Mahley RW. Apolipoprotein E2 transgenic rabbits. Modulation of the type III hyperlipoproteinemic phenotype by estrogen and occurrence of spontaneous atherosclerosis. J Biol Chem. 1997;272:22685–94.
Koike T, Liang J, Wang X, Ichikawa T, Shiomi M, Liu G, Sun H, Kitajima S, Morimoto M, Watanabe T, et al. Overexpression of lipoprotein lipase in transgenic Watanabe heritable hyperlipidemic rabbits improves hyperlipidemia and obesity. J Biol Chem. 2004;279:7521–9.
Hirata K, Dichek HL, Cioffi JA, Choi SY, Leeper NJ, Quintana L, Kronmal GS, Cooper AD, Quertermous T. Cloning of a unique lipase from endothelial cells extends the lipase gene family. J Biol Chem. 1999;274:14170–5.
Jaye M, Lynch KJ, Krawiec J, Marchadier D, Maugeais C, Doan K, South V, Amin D, Perrone M, Rader DJ. A novel endothelial-derived lipase that modulates HDL metabolism. Nat Genet. 1999;21:424–8.
Zhang J, Yu Y, Nakamura K, Koike T, Waqar AB, Zhang X, Liu E, Nishijima K, Kitajima S, Shiomi M, et al. Endothelial lipase mediates HDL levels in normal and hyperlipidemic rabbits. J Atheroscler Thromb. 2012;19:213–26.
Yu KC, David C, Kadambi S, Stahl A, Hirata K, Ishida T, Quertermous T, Cooper AD, Choi SY. Endothelial lipase is synthesized by hepatic and aorta endothelial cells and its expression is altered in apoE-deficient mice. J Lipid Res. 2004;45:1614–23.
Yasuda T, Ishida T, Rader DJ. Update on the role of endothelial lipase in high-density lipoprotein metabolism, reverse cholesterol transport, and atherosclerosis. Circ J. 2010;74:2263–70.
McCoy MG, Sun GS, Marchadier D, Maugeais C, Glick JM, Rader DJ. Characterization of the lipolytic activity of endothelial lipase. J Lipid Res. 2002;43:921–9.
Ishida T, Choi S, Kundu RK, Hirata K, Rubin EM, Cooper AD, Quertermous T. Endothelial lipase is a major determinant of HDL level. J Clin Invest. 2003;111:347–55.
Wang C, Nishijima K, Kitajima S, Niimi M, Yan H, Chen Y, Ning B, Matsuhisa F, Liu E, Zhang J, et al. Increased hepatic expression of endothelial lipase inhibits cholesterol diet-induced hypercholesterolemia and atherosclerosis in transgenic rabbits. Arterioscler Thromb Vasc Biol. 2017;37:1282–9.
Wang Y, Niimi M, Nishijima K, Waqar AB, Yu Y, Koike T, Kitajima S, Liu E, Inoue T, Kohashi M, et al. Human apolipoprotein A-II protects against diet-induced atherosclerosis in transgenic rabbits. Arterioscler Thromb Vasc Biol. 2013;33:224–31.
Ishida T, Choi SY, Kundu RK, Spin J, Yamashita T, Hirata K, Kojima Y, Yokoyama M, Cooper AD, Quertermous T. Endothelial lipase modulates susceptibility to atherosclerosis in apolipoprotein-E-deficient mice. J Biol Chem. 2004;279:45085–92.
Sorva R, Kuusi T, Dunkel L, Taskinen MR. Effects of endogenous sex steroids on serum lipoproteins and postheparin plasma lipolytic enzymes. J Clin Endocrinol Metab. 1988;66:408–13.
Galan X, Llobera M, Ramirez I. Lipoprotein lipase and hepatic lipase in Wistar and Sprague-Dawley rat tissues. Differences in the effects of gender and fasting. Lipids. 1994;29:333–6.
Khoo C, Campos H, Judge H, Sacks FM. Effects of estrogenic oral contraceptives on the lipoprotein B particle system defined by apolipoproteins E and C-III content. J Lipid Res. 1999;40:202–12.
Vigen R, O'Donnell CI, Baron AE, Grunwald GK, Maddox TM, Bradley SM, Barqawi A, Woning G, Wierman ME, Plomondon ME, et al. Association of testosterone therapy with mortality, myocardial infarction, and stroke in men with low testosterone levels. JAMA. 2013;310:1829–36.
Catakoglu AB, Kendirci M. Testosterone replacement therapy and cardiovascular events. Turk Kardiyol Dern Ars. 2017;45:664–72.
We thank Yoko Nakagawa for her technical assistance in making pathological specimens.
This work was supported in part by a research grant from the National Key Research and Development Program of China (No.2016YFE0126000), the National Natural Science Foundation of China (No.81800401, 81570392, 81770457, 81941001), JSPS KAKENHI Grant (15H04718), and JSPS-CAS under the Japan-China Research Cooperative Program.
Ethics approval and consent to participate
AII animal experiments were performed with the approval of the Animal Care Committee of the University of Yamanashi and Saga and conformed to the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Additional file 1: Figure S1.
Comparison of EL concentrations after castration in male and female rabbits. Rabbits were either on a chow diet or cholesterol-rich diet. Post-heparin plasma was collected and EL concentrations in pre- and post-orchiectomy or ovariectomy were measured using an EL ELISA kit from IBL (Gunma, Japan). Data are expressed as mean ± SD. n = 3–4 for each group.
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
About this article
Cite this article
Wang, C., Niimi, M., Kitajima, S. et al. Sex hormones affect endothelial lipase-mediated lipid metabolism and atherosclerosis. Lipids Health Dis 18, 226 (2019). https://doi.org/10.1186/s12944-019-1175-4
- Endothelial lipase
- Sex hormones
- Gender difference