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Biometric, nutritional, biochemical, and cardiovascular outcomes in male rats submitted to an experimental model of early weaning that mimics mother abandoning

Published online by Cambridge University Press:  09 September 2020

Rogério Barbosa de Magalhães Barros
Affiliation:
Fluminense Federal University, Niterói, Rio de Janeiro, Brazil
Thaís Alvim-Silva
Affiliation:
Fluminense Federal University, Niterói, Rio de Janeiro, Brazil
Júlia Raquel Nunes de Souza
Affiliation:
Fluminense Federal University, Niterói, Rio de Janeiro, Brazil
Emiliana Barbosa Marques
Affiliation:
Fluminense Federal University, Niterói, Rio de Janeiro, Brazil
Nazareth N. Rocha
Affiliation:
Fluminense Federal University, Niterói, Rio de Janeiro, Brazil
Fernanda C. F. Brito
Affiliation:
Fluminense Federal University, Niterói, Rio de Janeiro, Brazil
Christianne B. V. Scaramello*
Affiliation:
Fluminense Federal University, Niterói, Rio de Janeiro, Brazil
*
Address for correspondence: Christianne Bretas Vieira Scaramello, PhD, Fluminense Federal University, Rua Professor Hernani Pires de Melo, 101, Sala 204A, São Domingos, Niterói CEP 24.210-130, RJ, Brazil. Email: chrisbretas@gmail.com
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Abstract

Literature describes breast milk as the best food for the newborn, recommending exclusive breastfeeding for up to 6 months of age. However, it is not available for more than 40% of children worldwide. Pharmacological and non-pharmacological models of 3-day early weaning were developed in rodents to investigate later outcomes related solely to this nutritional insult. Thus, the present work aimed to describe biometric, nutritional, biochemical, and cardiovascular outcomes in adult male rats submitted to 3-day early weaning achieved by maternal deprivation. This experimental model comprises not only nutritional insult but also emotional stress, simulating mother abandoning. Male offspring were physically separated from their mothers at 21st (control) or 18th (early weaning) postnatal day, receiving water/food ad libitum. Analysis performed at postnatal days 30, 90, 150, and 365 encompassed body mass and food intake monitoring and serum biochemistry determination. Further assessments included hemodynamic, echocardiographic, and cardiorespiratory evaluation. Early-weaned males presented higher body weight when compared to control as well as dyslipidemia, higher blood pressure, diastolic dysfunction, and cardiac hypertrophy in adult life. Animals early deprived of their mothers have also presented a worse performance on the maximal effort ergometer test. This work shows that 3-day early maternal deprivation favors the development of cardiovascular disease in male rats.

Type
Original Article
Copyright
© The Author(s), 2020. Published by Cambridge University Press in association with the International Society for Developmental Origins of Health and Disease

Introduction

The research field named “Developmental Origins of Health and Disease” (DOHaD) aims to provide a clear perspective on how different life experiences modulate health and disease risks over a lifetime. This research field’s history reached a milestone with David Barker’s theory about the fetal origins of disease. After this, several studies, including animal research, confirmed the principle that early life affect cardiometabolic function in adulthood and elucidated some important underlying programming mechanisms.Reference Penkler, Hanson, Biesma and Müller1

Literature describes breast milk as the best food for the newborn. It potentially reduces infant mortality and protects against infection and diseases.Reference Victora, Smith and Vaughan2 As per several authors, such as Kramer and Kakuma, the World Health Organization (WHO) and the United Nations Children’s Fund (UNICEF) recommend exclusive breastfeeding up to 6 months of age. Exclusive breastfeeding excludes the consumption of any other food or drink besides breast milk, even water, throughout this period.Reference Kramer and Kakuma3 Despite this, it is estimated that exclusively breastfeeding is not available for no more than 40% of children worldwide along the first semester of life.4 Literature also reports that many women cannot breastfeed their children during this time, mainly those from lower social classes.5 Importantly, a growing body of evidence suggests that breastfeeding has a protective role against obesity, hypertension, dyslipidemia, and type 2 diabetes mellitus during adulthood.Reference Kelishadi and Farajian6

Different animal models of early weaning have already been developed in rodents. For example, there are pharmacological and non-pharmacological models that aim to suppress lactation 3 days earlier, considering standard weaning on postnatal day 21.Reference Souza, de Moura and Lisboa7 Bromocriptine administration in lactating female rats inhibits milk secretion, while bandages restrain the offspring’s access to the dams’ tits. As shared findings, these two experimental models have led to higher body mass and serum triglyceride (TG), as well as hyperleptinemia and central resistance to leptin in adulthood.Reference Bonomo, Lisboa, Passos, Passos-Moura, Reis and Moura8Reference Lima, Moura and Passos12 According to Quinn,Reference Quinn13 early weaning at postnatal day 18 mimics a child weaned at the age of 5 months.

However, unlike bromocriptine administration or breast bandages placement, early weaning achievement by maternal deprivation involves maternal milk restriction and maternal care restriction, simulating mother abandoning.Reference Souza, de Moura and Lisboa7 In this scenario, it is crucial to evaluate the offspring outcomes upon the introduction of emotional stress besides nutritional insult. Thus, the present work aimed to describe biometric, nutritional, biochemical, and cardiovascular outcomes in male Wistar rats submitted to maternal deprivation at postnatal day 18. We hypothesize that the combination of nutritional insult and emotional stress raises cardiovascular risk and programs cardiovascular disease.

Materials and methods

Experimental design

The procedures have followed the National Research Council (US) Institute for Laboratory Animal Research. Ethics Committee of Fluminense Federal University (Niteroi, Brazil) approved the use of animals (CEUA UFF812/2016) following the Guide for the Care and Use of Laboratory Animals (NIH Publication No. 8023, revised 1978). All rats received standard chow (Nuvilab®) and tap water ad libitum at controlled conditions (22 °C, 55–65% humidity, 12/12 h light/dark cycle).

The breeding laboratory of the university has provided Wistar rats used for mating (F0 generation). Male (n = 8) and female rats (n = 16) about 3 months of age and no kinship were mated (2 females for 1 male) for 5 days. Afterward, pregnant female rats placed in individual cages have spontaneously given birth to 10–12 puppies after 21 days of gestation, as expected (postnatal day 0). Litters mixing/adjustment (preferably six males/mother) and standard weaning occurred at postnatal days 1 and 21, respectively.Reference Koolhaas and Poole14 Accordingly to previous animal models of early weaning described by literature,Reference Bonomo, Lisboa, Passos, Passos-Moura, Reis and Moura8-Reference Lima, Moura and Passos12 the dams (F0 generation) and consequently their respective offspring (F1 generation) were divided into two groups at postnatal day 18 by simple randomization:

  • Control – offspring weaned at postnatal day 21.

  • Early weaning – offspring weaned at postnatal day 18.

Standard and early weaning encompassed offspring–mother physical separation (two animals/cage). There was a total of 96 rats from the F1 generation:

  • Control – 34 males housed in 17 cages (14 females discarded) – 8 litters.

  • Early weaning – 38 males housed in 19 cages (10 females discarded) – 8 litters.

Offspring analysis occurred at postnatal days 30, 90, 150 and 365. Excepting for biochemical analysis, whenever possible, data were collected precisely from the same rats at different ages (eight males/group). The animals from each group were randomly distributed between biochemical and the other assays.

Biometrical and nutritional analysis

Body weight was monitored twice a week until the end of the experimental period, always at the same hour. Nose-to-anus, abdominal, and thoracic length were measured using a measuring tape, allowing calculation of body mass index (BMI) and abdominal and thoracic lengths ratio. Daily food intake (g) was determined by subtracting the remaining chow by the total put in the cage the day before, dividing by the number of rats (two) per box. The summation of daily food intake throughout the interlude of interest gave the amount of food consumed in a given period.Reference Marques, Barros, Rocha and Scaramello15

It was possible to record data from all animals euthanized at postnatal day 365 (16 animals/group).

Echocardiographic and hemodynamic evaluation

Transthoracic echocardiography took place with anesthetized rats (ketamine 50 mg/kg plus xylazine 5 mg/kg intraperitoneally). The parameters recorded using a portable ultrasound (Siemens Accusion Cypress, Siemens AG, Munich, Germany) and a 10-MHz transducer to evaluate cardiac structure were interventricular septum (IVS) thickness, left ventricular posterior wall (LVPW) thickness, and left ventricular internal diameter (LVID) measured in diastole, as well as relative wall thickness (RWT), left ventricular mass (LVM), and left atrium to aorta ratio (LA/Ao). The parameters recorded to evaluate systolic and diastolic function were left ventricular ejection fraction and mitral deceleration time (MDT), respectively.Reference Lang, Bierig and Devereux16

Hemodynamic assessment occurred after 7 days of acclimation (10 min/day) in the morning. The animals submitted to the noninvasive tail-cuff method were awake (Insight, São Paulo, Brasil). Final values of systolic blood pressure (SBP) and diastolic blood pressure (DBP) represent the average of six measurements successfully acquired and gave mean arterial pressure (MAP) through the formula: MAP = SBP + 2(DBP/3).Reference Sousa, Hermann, Guimarães, Menezes and Carvalho17,Reference Fritz and Rinaldi18 Because of the assay’s stress bias, it was not always possible to record all available animals’ hemodynamic parameters. It was possible to achieve complete hemodynamic data from at least five animals per group.

Maximum effort ergometer test

After 4 days of acclimation, animals were individually submitted to a maximum effort test using a treadmill (Imbrasport®, Brasília, Brasil). Initial speed was 0.9 km/h being followed by progressive increments of 0.3 km/h every 3 min. The end of the test was determined when animals remained still for at least 10 s is considered exhausted. Distance, time spent, and maximum speed developed were recorded and posteriorly analyzed.Reference Molnar, Servais and Guichardant19,Reference Wonders, Hydock and Hayward20

Biochemical analysis

Serum samples were obtained by cardiac puncture after euthanasia using thiopental (100 mg/kg i.p) in fasting conditions and after 15 min of centrifugation at 1300×g (storage at −80 °C). Lipid profile was determined using a commercially available Labtest Brasil kit.Reference Marques, Motta and Kummerle21 Friedewald equationReference Friedewald, Levy and Fredrickson22 was applied to calculate low-density lipoproteins cholesterol (LDL-c) and very low-density lipoproteins cholesterol (VLDL-c) concentrations. The ratio of total cholesterol and high-density lipoproteins cholesterol (HDL-c) levels gave the Castelli I index. The ratio between LDL-c and HDL-c levels provided the Castelli II index.Reference Castelli, Garrison, Wilson, Abbott, Kalousdian and Kannel23 As another atherogenic index, the ratio between TGs and HDL-c concentrations was also evaluated.Reference Reaven24 Serum leptin levels were also determined using a commercially available kit of Enzyme-Linked Immunoabsorbent Assay (Rat Leptin ELISA, Millipore, Billerica, MA, USA).Reference Toste, de Moura, Lisboa, Fagundes, de Oliveira and Passos25

Due to hemolysis, it was impossible to analyze all serum samples, allowing assays with at least five samples from each group.

Statistical analysis

Data were analyzed using GraphPad Prism software version 7.0. Values are expressed as mean ± standard error of the mean. The Shapiro–Wilk test evaluated normality. Normally distributed data were analyzed applying Student’s unpaired t-test comparing control and early weaning groups within the same postnatal day. Significance was accepted when the p-value was < 0.05.

Results

Biometrical and nutritional analysis

Table 1 shows that early-weaned rats at postnatal day 30 presented a lower body weight than their respective controls. In contrast, older animals presented a higher body weight, reflecting lower BMI in youth and a greater abdominal and thoracic circumferences ratio in the elderly. Food intake increased from postnatal day 90 upward (Fig. 1).

Table 1. Biometric parameters

Data are represented as mean ± SEM.

*p < 0.05 between control and early weaning groups at the same postnatal day (Student’s t-test).

Fig. 1. Nutritional parameter. Food intake (g). Data are represented as mean ± SEM. *p < 0.05 between control and early weaning groups at the same period (Student’s t-test). n = 16/group.

Echocardiographic and hemodynamic evaluation

Table 2 shows data from echocardiographic studies and hemodynamic evaluation. There were differences between early-weaned rats and their respective controls at postnatal days 90, 150, and 365. IVS thickness and LVPW thickness, both measured in diastole, as well as LVM, were founded increased in early-weaned rats upward postnatal day 90. However, there were distinguished parameters in specific moments. Animals at postnatal day 90 presented higher left ventricular RWT, LA/Ao ratio, and DBP/mean blood pressure. Rats at postnatal day 365 also exhibited an increased LA/Ao ratio but accompanied by a superior SBP and reduced LVID and MDT. Animals at postnatal day 150 have presented higher values of SBP, DBP, and mean blood pressure. It was also observed higher values of DBP and mean blood pressure at postnatal day 90, while only SBP was increased at postnatal day 365.

Table 2. Echocardiographic and hemodynamic parameters

LVEF, left ventricular ejection fraction; LA/Ao, left atrium to aorta ratio; IVSd, intraventricular septum thickness in diastole; LVPWd, left ventricular posterior wall thickness in diastole; LVIDd, left ventricular internal diameter in diastole; RWT, relative wall thickness; LVM, left ventricular mass; MDT, mitral deceleration time; SBP, systolic blood pressure; DBP, diastolic blood pressure; MAP, mean arterial pressure.

Data are represented as mean ± SEM.

*p < 0.05 between control and early weaning groups at the same postnatal day (Student’s t-test).

Maximum effort ergometer test

There were differences in exercise tolerance between groups only in elderly animals. Early-weaned rats at postnatal day 365 have presented a less lasting test, traveling a shorter distance and reaching an inferior maximum speed compared to respective controls (Table 3).

Table 3. Data from maximum effort ergometer test

Data are represented as mean ± SEM.

*p < 0.05 between control and early weaning groups at the same postnatal day (Student’s t-test).

Biochemical analysis

Serum levels of TGs and VLDL-c, as well as TG/HDL-c ratio, were found higher in early-weaned rats since postnatal day 30. Besides, the Castelli I index was increased in these animals compared to respective controls since postnatal day 150, while HDL concentration was decreased only at postnatal day 365 (Table 4).

Table 4. Biochemical parameters

TG, triglyceride; LDL-c, low density lipoproteins cholesterol; VLDL-c, very low-density lipoproteins cholesterol; HDL-c, high density lipoproteins cholesterol.

Data are represented as mean ± SEM.

*p < 0.05 and **p < 0.01 between control and early weaning groups at the same postnatal day (Student’s t-test).

There were also differences in leptin serum levels (Table 4). Its concentration was higher in early-weaned rats since postnatal 150.

Discussion

The present study has shown an early weaning model achieved by maternal deprivation that combines nutritional insult and emotional stress. It was capable of raising cardiometabolic risk since youth, allowing cardiovascular disease development in adulthood/elderly. We found that early-weaned male rats presented higher body mass, SBP, and impaired serum lipid profile than controls. Besides, diastolic dysfunction associated with a suggestive pattern of cardiac hypertrophy, as well as exercise intolerance, was also observed in these animals.

Soon after early weaning, 30-day-old rats have presented lower body weight and BMI than controls, as reported in previous studies involving mother–offspring separationReference McIntosh, Anisman and Merali26, bromocriptine administration,Reference Bonomo, Lisboa, Pereira, Passos and de Moura9 and bandages.Reference Lima, Moura and Passos12 Thus, these data validate the proposed experimental model of malnutrition during lactation.

Upward postnatal day 150, early-weaned rats have presented a slightly higher body weight than controls, accompanied by hyperphagia, since postnatal day 90. This observation may be due to ‘catch-up growth’ defined by Wit and BoersmaReference Wit and Boersma27 as an accelerated growth after a period of its inhibition determined by early undernutrition. In elderly animals, there was an increased abdominal/thoracic circumferences ratio. According to literature, this profile is related to a higher cardiometabolic risk.Reference Huxley, Mendis, Zheleznyakov, Reddy and Chan28

Dyslipidemic profile corroborates the increase in cardiovascular disease risk, worsened with aging. There were higher plasma levels of TG and VLDL-c, as well as increased TG/HDL-c ratio since postnatal day 30, followed by the rise of the Castelli index and the decrease in HDL-c levels. Dyslipidemic profile was also observed in different models of early weaning.Reference Moura, Bonomo and Neto10,Reference Lima, Moura and Passos12,Reference Franco, Lisboa and Lima29 Experimental studies have shown that hypertriglyceridemia is a risk factor for coronary heart disease, regardless of overweight. TG-rich lipoproteins, particularly VLDLs, have a direct atherogenic effect.Reference Murad, Hazem and Coto-Yglesias30-Reference Havel and Hamilton32 VLDLs are hydrolyzed in the liver by lipase and converted to LDL particles, a crucial trigger of atherosclerosis genesis that favors lipid deposition in vessels.Reference Brown and Goldstein33-Reference Klop, Elte and Cabezas35 Besides, HDL-c has a protective role partly due to its ability to remove intracellular cholesterol and perform reverse transport, allowing its redistribution in the body and biliary excretion.Reference Rizzo, Otvos, Nikolic, Montalto, Toth and Banach36 HDL-c presents antioxidant and anti-inflammatory properties, inactivating or preventing oxidation of phospholipids from LDL-c.Reference Gogonea37,Reference Dobiásová38 HDL-c also inhibits apoptosis of endothelial cells and is associated with a relevant antiatherogenic action.Reference Klop, Elte and Cabezas35-Reference Gogonea37. According to literature, the Castelli I index and TG/HDL ratio are atherogenic markers. They are useful instruments to predict coronary artery disease risk in daily practice, especially in people with other risk factors.Reference Marques, Motta and Kummerle21,Reference Reaven24,Reference Sayın, Kutlu and Koçak39

Leptin serum levels have also increased in early-weaned male rats upward postnatal day 150. Usually, leptin increases the expression of neuropeptides associated with food intake inhibition. Proopimelanocortin, as well as cocaine and amphetamine-regulated transcripts, stimulates total energy expenditure via sympathetic activation. Besides, it decreases the expression of neuropeptide Y and agouti-related protein, associated with increased food intake and reduced energy expenditure.Reference Sayın, Kutlu and Koçak39 Leptin plays an essential role in regulating energy homeostasis, decreasing appetite and increasing energy expenditure. Thus, the hyperphagia and the higher body weight suggest leptin hypothalamic resistance. Hyperphagia, higher body mass, and TG/leptin serum levels as well as leptin resistance outcomes were also observed in previous studies encompassing other animal models of early weaning.Reference Moura, Bonomo and Neto10,Reference Bonomo, Lisboa, Passos, Alves, Reis and de Moura11,Reference Franco, Lisboa and Lima29,Reference Pietrobon, Bertasso and Silva41,Reference Lima, Moura and Franco42

Early-weaned rats presented higher LVM, IVS thickness and LVPW thickness, both in diastole, compared to respective adult and elderly controls. RWT was higher in this group at postnatal day 90 but not 150 or 365. These data point to concentric remodeling that evolved into eccentric patterns commonly observed in patients with diastolic heart failure.Reference Nagueh, Appleton and Gillebert43 The observed increase in LA/Ao diameter ratio suggests pressure raise in LA and consequently dilatation of its cavity, possibly due to ventricular relaxation impairment during diastole.Reference Hoss, Petterson and Scherer44,Reference Boon45 MDT, intimately related to left ventricular compliance, was shorter in early-weaned animals characterizing diastolic dysfunction and left atrial dilatation does.Reference Nagueh, Appleton and Gillebert43

The maximal effort ergometer test infers the cardiorespiratory capacity.Reference Marques, Barros, Rocha and Scaramello15 There is a linear relationship between maximum speed developed by the animal and its oxygen uptake rate.Reference Rodrigues, Figueroa, Mostarda, Heeren, Irigoyen and De Angelis46 Thus, a less lasting test accompanied by a shorter distance traveled and an inferior maximum speed described to elderly early-weaned rats suggest a diminished tolerance to exercise compared to respective controls. Diastolic dysfunction favors exercise intolerance.Reference Cohen-Solal, Beauvais and Tabet47 It is noteworthy that maximum cardiac output during exercise is dependent on diastolic filling. If relaxation abnormalities accompany diastole, lower ventricular filling rates are achieved and become insufficient to supply cardiac output required during exercise sessions. Consequently, filling pressure increases and maximum capacity decreases; thus, as diastolic dysfunction progresses, the lower will become exercise capacity.Reference Otto, Pereira, Beck and Milani48,Reference Little, Kitzman and Cheng49

Early-life stress is also a relevant factor involved in metabolic programming.Reference Souza, de Moura and Lisboa7 Despite this, biometric, nutritional, and biochemical outcomes here described are similar to those observed in studies using pharmacological and non-pharmacological models of early weaning that avoid emotional stress.Reference Bonomo, Lisboa, Passos, Passos-Moura, Reis and Moura8-Reference Lima, Moura and Passos12,Reference Franco, Lisboa and Lima29,Reference Pietrobon, Bertasso and Silva41,Reference Lima, Moura and Franco42

According to Tractenberg et al.,Reference Tractenberg, Levandowski and de Azeredo50 maternal deprivation protocols present methodological pitfalls due to different degrees of stress exposure in maternal separation-reared pups. Nevertheless, here we took care of important methodological issues to avoid bias, such as housing/husbandry conditions, animal/standard facility rearing, and litter controls.

Kikusui, Ichikawa, and MoriReference Kikusui, Ichikawa and Mori51 observed that mice weaned on postnatal day 14 showed a prolonged increase in corticosterone compared to the littermates stayed with dam until postnatal day 21. The last ones have presented a transient increase. Moura et al. Reference Moura, Bonomo and Neto10 also reported hypercorticosteronaemia and higher total catecholamine levels later in life. According to Huang et al.,Reference Huang, White, Ahmad and Leenen52 hypercorticosteronemia could explain the higher blood pressure seen because glucocorticoids increase blood pressure. For instance, hypertension is often associated with left ventricular hypertrophy and heart failure with preserved ejection fraction, that impair exercise tolerance, outcomes described in this study.Reference Otto, Pereira, Beck and Milani48,Reference Little, Kitzman and Cheng49,Reference Dickstein, Cohen-Solal and Filippatos53,Reference Montera, Almeida and Tinoco54

Literature report that adaptation mechanisms may be different between sexes in early weaning models.Reference Souza, de Moura and Lisboa7 Nevertheless, our main objective was to describe outcomes in male rats submitted to an early weaning model encompassing an emotional stress, as widely performed with pharmacological and non-pharmacological models.

The measurement of corticosterone level would contribute to a better understanding of this model, although not compromise the relevance of our findings. Along with corticosterone measurement, sexual dimorphism also encompasses a perspective for future studies in this experimental model.

In conclusion, the present work demonstrates, for the first time, cardiovascular disease development in later life due to maternal deprivation at postnatal day 18. This early weaning model simulates mother abandoning, a social health challenge. As cardiovascular diseases are the leading death causes worldwide, public policies favoring exclusive breastfeeding until 6 months of age may constitute an important strategy to reduce their incidence, reducing direct and indirect health expenditures.

Acknowledgments

The authors thank FAPERJ, CAPES, and CNPq for the financial support.

Conflict of interests

The authors declare no conflict of interest.

References

Penkler, M, Hanson, M, Biesma, R, Müller, R. DOHaD in science and society: emergent opportunities and novel responsibilities. J DOHaD. 2018; 10(3),268273. doi: 10.1017/S2040174418000892 Google ScholarPubMed
Victora, CG, Smith, PG, Vaughan, JP et al. Evidence for protection by breastfeeding against infant deaths from infectious diseases in Brazil. Lancet (Br Edn). 1987; 330: 319322.CrossRefGoogle Scholar
Kramer, MS, Kakuma, R. Optimal duration of exclusive breastfeeding. Cochrane Database Syst Rev. 2012; 8(CD003517), 195. doi: 10.1002/14651858.CD003517.pub2 Google Scholar
WHO. Infant and Young Child Feeding. IOP Publishing WHO. 2017; http://www.who.int/mediacentre/factsheets/fs342/en/. Accessed 17 September 2019Google Scholar
UNICEF and WHO. GLOBAL BREASTFEEDING INVESTMENT CASE. IOP Publishing WHO. http://who.int/nutrition/publications/infantfeeding/global-bf-collective-investmentcase/en/. Accessed 12 December 2019Google Scholar
Kelishadi, R, Farajian, S. The protective effects of breastfeeding on chronic non-communicable diseases in adulthood: a review of evidence. Adv Biomed Res. 2014; 3, 3. doi: 10.4103/2277-9175.124629 CrossRefGoogle ScholarPubMed
Souza, LL, de Moura, EG, Lisboa, PC. Does early weaning shape future endocrine and metabolic disorders? Lessons from animal models. J Dev Orig Health Dis. 2020; 111. doi: 10.1017/S2040174420000410 Google ScholarPubMed
Bonomo, IT, Lisboa, PC, Passos, MC, Passos-Moura, C, Reis, AM, Moura, EG. Prolactin inhibition in lactating rats changes leptin transfer through the milk. Horm Metab Res. 2005; 37(4), 220225. doi: 10.1055/s-2005-861381 CrossRefGoogle ScholarPubMed
Bonomo, IT, Lisboa, PC, Pereira, AR, Passos, MC, de Moura, EG. Prolactin inhibition in dams during lactation programs for overweight and leptin resistance in adult offspring. J Endocrinol. 2007; 192(2), 339344. doi: 10.1677/joe.1.06952 CrossRefGoogle ScholarPubMed
Moura, EG, Bonomo, IT, Neto, JF, et al. Maternal prolactin inhibition during lactation programs for metabolic syndrome in adult progeny. J Physiol. 2009; 587 (20), 49194929. doi: 10.1113/jphysiol.2009.176289 CrossRefGoogle ScholarPubMed
Bonomo, IT, Lisboa, PC, Passos, MC, Alves, SB, Reis, AM, de Moura, EG. Prolactin inhibition at the end of lactation programs for a central hypothyroidism in adult rat. J Endocrinol. 2008; 198, 331337. doi: 10.1677/JOE-07-0505 CrossRefGoogle ScholarPubMed
Lima, NS, Moura, EG, Passos, MC, et al. Early weaning causes undernutrition for a short period and programmes some metabolic syndrome components and leptin resistance in adult rat offspring. Br J Nutr. 2011; 105(9), 14051413. doi: 10.1017/S0007114510005064 CrossRefGoogle Scholar
Quinn, R. Comparing rat’s to human’s age: how old is my rat in people years? Nutrition. 2005; 21(6), 775777. doi: 10.1016/j.nut.2005.04.002 CrossRefGoogle ScholarPubMed
Koolhaas, JM. The laboratory rat. In The UFAW Handbook on the Care and Management of Laboratory Animals (ed. Poole, T), 2006; pp. 313330. 7th ed. British: Blackwell Science.Google Scholar
Marques, EB, Barros, RBM, Rocha, NN, Scaramello, CBV. Aging and cardiac, biochemical, molecular and functional changes: experimental study. Int J Cardiovasc Sci. 2015; 1(1), 4250. doi: 10.5935/2359-4802.20150007 Google Scholar
Lang, RM, Bierig, M, Devereux, RB, et al. Recommendations for chamber quantification: a report from the American Society of Echocardiography’s Guidelines and Standards Committee and the Chamber Quantification Writing Group, developed in conjunction with the European Association of Echocardiography, a branch of the European Society of Cardiology. J Am Soc Echocardiogr. 2005; 18(12), 14401463. doi: 10.1016/j.echo.2005.10.005 CrossRefGoogle ScholarPubMed
Sousa, JMA, Hermann, JLV, Guimarães, JB, Menezes, PPO, Carvalho, ACC. Avaliação das Pressões Sistólica, Diastólica e Pressão de Pulso como Fator de Risco para Doença Aterosclerótica Coronariana Grave em Mulheres com Angina Instável ou Infarto Agudo do Miocárdio sem Supradesnivelamento do Segmento ST. Arq Bras Cardiol. 2004; 82 (5), 426429. doi: 10.1590/S0066-782X2004000500005 CrossRefGoogle Scholar
Fritz, M, Rinaldi, G. Influence of nitric oxide-mediated vasodilation on the blood pressure measured with the tail-cuff method in the rat. J Biomed Sci. 2007; 14(6), 757765. doi: 10.1007/s11373-007-9191-1 CrossRefGoogle ScholarPubMed
Molnar, AM, Servais, S, Guichardant, M, et al. Mitochondrial H2O2 production is reduced with acute and chronic eccentric exercise in rat skeletal muscle. Antioxid Redox Signal. 2006; 8(3–4), 548558. doi: 10.1089/ars.2006.8.548 CrossRefGoogle ScholarPubMed
Wonders, KY, Hydock, DS, Hayward, R. Time-course of changes in cardiac function during recovery after acute exercise. Appl Physiol Nutr Metab. 2007; 32(6), 11641169. doi: 10.1139/H07-127 CrossRefGoogle ScholarPubMed
Marques, EB, Motta, NAV, Kummerle, AE, et al. In vivo effect of LASSBio-785, a lipid-lowering and anti-inflammatory agent, on cardiac Ca2+-ATPases from hypercholesterolemic rats. Int J Cardiol. 2015; 201, 282284. doi: 10.1016/j.ijcard.2015.08.091 CrossRefGoogle Scholar
Friedewald, WT, Levy, RI, Fredrickson, DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972; 18(6), 499502.CrossRefGoogle ScholarPubMed
Castelli, WP, Garrison, RJ, Wilson, PW, Abbott, RD, Kalousdian, S, Kannel, WB. Incidence of coronary heart disease and lipoprotein cholesterol levels. The Framingham Study. JAMA. 1986; 256(20), 28352838. doi: 10.1001/jama.1986.03380200073024 CrossRefGoogle ScholarPubMed
Reaven, G. Metabolic syndrome: pathophysiology and implications for management of cardiovascular disease. Circulation. 2002; 106(3), 286288. doi: 10.1161/01.CIR.0000019884.36724.D9 CrossRefGoogle ScholarPubMed
Toste, FP, de Moura, EG, Lisboa, PC, Fagundes, AT, de Oliveira, E, Passos, MC. Neonatal leptin treatment programmes leptin hypothalamic resistance and intermediary metabolic parameters in adult rats. Br J Nutr. 2006; 95(4), 830837. doi: 10.1079/BJN20061726 CrossRefGoogle ScholarPubMed
McIntosh, J, Anisman, H, Merali, Z. Short- and long-periods of neonatal maternal separation differentially affect anxiety and feeding in adult rats: gender-dependent effects. Dev Brain Res. 1999; 113(1–2), 97106. doi: 10.1016/S0165-3806(99)00005-X CrossRefGoogle Scholar
Wit, JM, Boersma, B. Catch up growth: definition, mechanisms, and models. J Pediatr Endocrinol Metab. 2002; 15 (Suppl. 5), 12291241.Google ScholarPubMed
Huxley, R, Mendis, S, Zheleznyakov, E, Reddy, S, Chan, J. Body mass index, waist circumference and waist:hip ratio as predictors of cardiovascular risk – a review of the literature. Eur J Clin Nutr. 2010; 64(1), 1622. doi: 10.1038/ejcn.2009.68 CrossRefGoogle ScholarPubMed
Franco, JG, Lisboa, PC, Lima, NS, et al. Resveratrol attenuates oxidative stress and prevents steatosis and hypertension in obese rats programmed by early weaning. J Nutr Biochem. 2013; 24(6), 960966. doi: 10.1016/j.jnutbio.2012.06.019 CrossRefGoogle ScholarPubMed
Murad, MH, Hazem, A, Coto-Yglesias, F, et al. The association of hypertriglyceridemia with cardiovascular events and pancreatitis: systematic review and meta-analysis. BMC Endocr Disord. 2012; 12, 2. doi: 10.1186/1472-6823-12-2 CrossRefGoogle ScholarPubMed
Borén, J, Matikainen, N, Adiels, M, Taskinen, MR. Postprandial hypertriglyceridemia as a coronary risk factor. Clin Chim Acta. 2014; 431, 131142. doi: 10.1016/j.cca.2014.01.015 CrossRefGoogle ScholarPubMed
Havel, RJ, Hamilton, RL. Hepatocytic lipoprotein receptors and intracellular lipoprotein catabolism. Hepatology. 1988; 8(6), 16891704. doi: 10.1002/hep.1840080637 CrossRefGoogle ScholarPubMed
Brown, MS, Goldstein, JL. Biomedicine. Lowering LDL – not only how low, but how long? Science. 2006; 311(5768), 17211723. doi: 10.1126/science.1125884 CrossRefGoogle ScholarPubMed
Varbo, A, Benn, M, Smith, GD, Timpson, NJ, Tybjaerg-Hansen, A, Nordestgaard, BG. Remnant cholesterol, low-density lipoprotein cholesterol, and blood pressure as mediators from obesity to ischemic heart disease. Circ Res. 2015; 116 (4), 665673. doi: 10.1161/CIRCRESAHA.116.304846 CrossRefGoogle ScholarPubMed
Klop, B, Elte, JW, Cabezas, MC. Dyslipidemia in obesity: mechanisms and potential targets. Nutrients. 2013; 5(4), 12181240. doi: 10.3390/nu5041218 CrossRefGoogle ScholarPubMed
Rizzo, M, Otvos, J, Nikolic, D, Montalto, G, Toth, PP, Banach, M. Subfractions and subpopulations of HDL: an update. Curr Med Chem. 2014; 21(25), 28812891. doi: 10.2174/0929867321666140414103455 CrossRefGoogle ScholarPubMed
Gogonea, V. Structural insights into high density lipoprotein: old models and new facts. Front Pharmacol. 2016; 6, 318. doi: 10.3389/fphar.2015.00318 CrossRefGoogle ScholarPubMed
Dobiásová, M. Atherogenic index of plasma [log(triglycerides/HDL-cholesterol)]: theoretical and practical implications. Clin Chem. 2004; 50(7), 11131115. doi: 10.1373/clinchem.2004.033175 CrossRefGoogle ScholarPubMed
Sayın, S, Kutlu, R, Koçak, A. The relationship between atherogenic index of plasma and major risk factors of cardiovascular disease in obese and nonobese individuals. Eur Res J. 2019; 5(4), 678685. doi: 10.18621/eurj.414561 Google Scholar
Fonseca-Alaniz, MH, Takada, J, Alonso-Vale, MIC, Lima, FB. O tecido adiposo como centro regulador do metabolismo. Arq Bras Endocrinol Metab. 2006; 50(2), 216229. doi: 10.1590/S0004-27302006000200008 CrossRefGoogle Scholar
Pietrobon, CB, Bertasso, IM, Silva, BS, et al. Body adiposity and endocrine profile of female Wistar rats of distinct ages that were early weaned. Horm Metab Res. 2020; 52(1), 5866. doi: 10.1055/a-0966-8784 Google ScholarPubMed
Lima, NS, Moura, EG, Franco, JG, et al. Developmental plasticity of endocrine disorders in obesity model primed by early weaning in dams. Horm Metab Res. 2013; 45(1), 2230. doi: 10.1055/s-0032-1323703 Google ScholarPubMed
Nagueh, SF, Appleton, CP, Gillebert, TC, et al. Recommendations for the evaluation of left ventricular diastolic function by echocardiography. Eur J Echocardiogr 2009; 10(2), 165193. doi: 10.1016/j.echo.2008.11.023 CrossRefGoogle ScholarPubMed
Hoss, AJ, Petterson, CHP, Scherer, L. Miocardiopatia hipertrófica. Papel da ecocardiografia doppler no diagnóstico e na orientação terapêutica. Arq Bras Cardiol 1998; 70(4), 301306. doi: 10.1590/S0066-782X1998000400012 CrossRefGoogle Scholar
Boon, JA. Manual of Veterinary Echocardiography, 1998; pp. 478. Williams and Wilkins, Baltimore.Google Scholar
Rodrigues, B, Figueroa, DM, Mostarda, CT, Heeren, MV, Irigoyen, MC, De Angelis, K. Maximal exercise test is a useful method for physical capacity and oxygen consumption determination in streptozotocin-diabetic rats. Cardiovasc Diabetol. 2007; 6 (38). doi: 10.1186/1475-2840-6-38 CrossRefGoogle ScholarPubMed
Cohen-Solal, A, Beauvais, F, Tabet, JY. Physiology of the abnormal response of heart failure patients to exercise. Curr Cardiol Rep. 2004; 6(3), 176181. doi: 10.1007/s11886-004-0020-0 CrossRefGoogle ScholarPubMed
Otto, MEB, Pereira, MM, Beck, ALS, Milani, M. Correlação da função diastólica com a capacidade máxima de exercício ao teste ergométrico. Arq. Bras. Cardiol. 2011; 96(2), 107113. doi: 10.1590/S0066-782X2011005000004 CrossRefGoogle Scholar
Little, WC, Kitzman, DW, Cheng, CP. Diastolic dysfunction as a cause of exercise intolerance. Heart Fail Rev. 2000; 5(4), 301306. doi: 10.1023/a:1026503028065 CrossRefGoogle ScholarPubMed
Tractenberg, SG, Levandowski, M, de Azeredo, LA et al. An overview of maternal separation effects on behavioural outcomes in mice: evidence from a four-stage methodological systematic review. Neurosci Biobehav Rev. 2016; 68, 489503. doi: 10.1016/j.neubiorev.2016.06.021 CrossRefGoogle ScholarPubMed
Kikusui, T, Ichikawa, S, Mori, Y. Maternal deprivation by early weaning increases corticosterone and decreases hippocampal BDNF and neurogenesis in mice. Psychoneuroendocrinology 2009; 34(5), 762772.CrossRefGoogle ScholarPubMed
Huang, BS, White, RA, Ahmad, M, Leenen, F. Role of brain corticosterone and aldosterone in central angiotensin II-induced hypertension. Hypertension. 2013; 62, 564571. http://dx.doi.org/10.1161/HYPERTENSIONAHA.113.01557 CrossRefGoogle ScholarPubMed
Dickstein, K, Cohen-Solal, A, Filippatos, G, et al. ESC Committee for Practice Guidelines (CPG). ESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2008: the Task Force for the diagnosis and treatment of acute and chronic heart failure 2008 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association of the ESC (HFA) and endorsed by the European Society of Intensive Care Medicine (ESICM). Eur J Heart Fail. 2008; 10(10), 933989. doi: 10.1016/j.ejheart.2008.08.005 CrossRefGoogle Scholar
Montera, MW, Almeida, RA, Tinoco, EM et al. Sociedade Brasileira de Cardiologia. II Diretriz Brasileira de Insuficiência Cardíaca Aguda. Arq Bras Cardiol. 2009; 93(3 Suppl. 3), 165. doi: 10.1590/S0066-782X2009001900001 Google Scholar
Figure 0

Table 1. Biometric parameters

Figure 1

Fig. 1. Nutritional parameter. Food intake (g). Data are represented as mean ± SEM. *p < 0.05 between control and early weaning groups at the same period (Student’s t-test). n = 16/group.

Figure 2

Table 2. Echocardiographic and hemodynamic parameters

Figure 3

Table 3. Data from maximum effort ergometer test

Figure 4

Table 4. Biochemical parameters