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Brazilian Journal of Medical and Biological Research

On-line version ISSN 1414-431X

Braz J Med Biol Res vol.45 no.10 Ribeirão Preto Oct. 2012 Epub May 31, 2012

http://dx.doi.org/10.1590/S0100-879X2012007500091 

Braz J Med Biol Res, October 2012, Volume 45(10) 982-987

Behavioral meaningful opioidergic stimulation activates kappa receptor gene expression

E. Teodorov1, M.F.R. Ferrari2, D.R. Fior-Chadi3, R. Camarini4 and L.F. Felício5

1Centro de Matemática, Computação e Cognição, Universidade Federal do ABC, São Paulo, SP, Brasil
2Departamento de Genética e Biologia Evolutiva, Instituto de Biociências, Universidade de São Paulo, São Paulo, SP, Brasil
3Departamento de Fisiologia, Instituto de Biociências, Universidade de São Paulo, São Paulo, SP, Brasil
4Departamento de Farmacologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, SP, Brasil
5Departamento de Patologia, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, SP, Brasil

Abstract
Introduction
Material and Methods
Results
Discussion
References
Acknowledgments
Correspondence and Footnotes


Abstract

The periaqueductal gray (PAG) has been reported to be a location for opioid regulation of pain and a potential site for behavioral selection in females. Opioid-mediated behavioral and physiological responses differ according to the activity of opioid receptor subtypes. The present study investigated the effects of the peripheral injection of the kappa-opioid receptor agonist U69593 into the dorsal subcutaneous region of animals on maternal behavior and on Oprk1 gene activity in the PAG of female rats. Female Wistar rats weighing 200-250 g at the beginning of the study were randomly divided into 2 groups for maternal behavior and gene expression experiments. On day 5, pups were removed at 7:00 am and placed in another home cage that was distant from their mother. Thirty minutes after removing the pups, the dams were treated with U69593 (0.15 mg/kg, sc) or 0.9% saline (up to 1 mL/kg) and after 30 min were evaluated in the maternal behavior test. Latencies in seconds for pup retrieval, grouping, crouching, and full maternal behavior were scored. The results showed that U69593 administration inhibited maternal behavior (P < 0.05) because a lower percentage of U69593 group dams showed retrieval of first pup, retrieving all pups, grouping, crouching and displaying full maternal behavior compared to the saline group. Opioid gene expression was evaluated using real-time reverse-transcription polymerase chain reaction (RT-PCR). A single injection of U69593 increased Oprk1 PAG expression in both virgin (P < 0.05) and lactating female rats (P < 0.01), with no significant effect on Oprm1 or Oprd1 gene activity. Thus, the expression of kappa-opioid receptors in the PAG may be modulated by single opioid receptor stimulation and behavioral meaningful opioidergic transmission in the adult female might occur simultaneously to specific changes in gene expression of kappa-opioid receptor subtype. This is yet another alert for the complex role of the opioid system in female reproduction.

Key words: Real-time reverse-transcription polymerase chain reaction; Opioid receptor; Gene expression; Opioid sensitivity; Kappa opioid receptor


Introduction

Opioidergic stimuli modulate various sensory systems with behavioral consequences for both male and female mammals (1-9). The periaqueductal gray (PAG) is likely to influence a number of brainstem sites that are critically involved in controlling both somatomotor (e.g., mating) and autonomic (e.g., thermoregulation) responses, as well as hypothalamic regions related to the control of generalized arousal and sensorimotor integration (10,11). The PAG is also known to play important roles in the modulation of nociceptive sensory transmission, regulation of the cardiovascular system (12), vocalization (13), and expression of a variety of behaviors, including defensive (14), sexual (15), maternal (16-18), and feeding behaviors (15,19,20). The PAG occupies a pivotal position in the central nervous system that influences the selection of adaptive behavioral responses. This region receives both limbic information and a vast array of inputs from prefrontal cortical areas (21,22). Previous studies from our laboratory have suggested an integrative role of opioidergic transmission in the PAG in influencing behavioral selection during lactation (6,23-25). The role played by the PAG in maternal behavior may be dependent on adequate local expression of opioid-related genes.

Opioid receptors have been the focus of intense molecular, physiological, and pharmacological research. The PAG has a high density of opioid receptors and activation of these metabotropic, G-protein-coupled receptors modulates various aspects of reproductive behavior in females. There are three types of opioid receptors: mu, delta, and kappa (26). Multiple reproductive experiences influence both gene activity and opioid receptor expression in the PAG. A preliminary study suggested that opioidergic stimulation modulates opioid gene expression in the female PAG (27,28).

Our group has shown that the morphine-induced inhibition of maternal behavior is plastic and adaptive and that opioidergic transmission in the rostral PAG plays a role in this process. In addition, it has been demonstrated that both repeated treatment with morphine and reproductive experience have effects on the expression of opioid receptors. The present study further extends this line of research by investigating the hypothesis that one stimulation would modify the activity of a specific receptor gene. Although the major target of morphine and naloxone is Oprm1, the acute inhibition of maternal behavior induced by kappa receptor stimulation needs more investigation. Because kappa stimulation is behaviorally meaningful, this study was designed to specifically investigate the dynamics of kappa on the PAG. In order to test for indirect or nonspecific effects, the kappa activity of Oprm1 and Oprd1 was also measured.

The present study investigated the effects of U69593, a kappa-opioid receptor agonist, on mu-, kappa-, and delta-opioid receptor Oprm1, Oprk1, and Oprd1 gene activity in the PAG of both lactating and virgin female rats. This was performed by evaluating opioid gene expression using real-time reverse-transcription polymerase chain reaction (RT-PCR).

The aim of the present study was to determine whether a single kappa opioidergic stimulation using the kappa agonist U69593 can promote immediate changes in the activity and expression of the kappa-opioid receptor gene in the PAG of female animals. In order to test for indirect effects of such kappa stimulation on other opioid receptor genes, the activity of mu and delta receptor genes was also measured. Both virgin and lactating rats were tested to determine whether the physiological state influences the response to this agonist.


Material and Methods

Animals and housing

Female Wistar rats weighing 200-250 g at the beginning of the study were obtained from Faculdade de Medicina Veterinária, Universidade de São Paulo. The animals were housed in polypropylene cages (32 x 40 x 18 cm) with 3 animals per cage, under conditions of controlled temperature (22 ± 2°C), a 12/12-h light/dark cycle (lights on at 6:00 am), and free access to food and water during the experimental procedure. All animal procedures were in accordance with the guidelines of the Committee on the Care and Use of Laboratory Animal Resources, National Research Council, USA. We attempted to minimize the number of rats used, and every effort was made to ensure that no rat suffered unnecessarily.

For mating, 2 female rats were placed overnight with 1 sexually experienced male rat. The day on which sperm was observed in the vaginal lavage was designated day 1 of pregnancy. Pregnant rats were housed 2 per cage until day 18 of pregnancy and then individually until the end of the experiments. At parturition, all pups were examined externally, sexed, and weighed, with 8 pups (4 males and 4 females) left with each dam until the maternal behavior test (experiment 1) and gene expression studies (experiment 2).

Maternal tasks

On day 5 of lactation, pups were removed at 7:00 am and placed in another home cage that was distant from their mother. Thirty minutes after removing the pups, the dams were acutely challenged with U69593 ([5-α,7-α,8-β]-[+]-N-methyl-N-{7-(1-pyrrolidinyl)-1-oxaspiro[4.5]dec-8-yl}benzeneacetamide; Sigma Aldrich, USA, 0.15 mg/kg, sc) or saline. Thirty minutes after the injections were given to the dams, all pups were placed back with their mothers, and maternal behavior testing began. Latencies in seconds for pup sniffing, retrieval, grouping, crouching, and full maternal behavior were scored (2,3). Animals were scored as fully maternal if they retrieved all 8 pups to the nest and displayed nursing behavior with their back arched over the pups for 3 consecutive minutes. If animals were not fully maternal after 30 min of continuous observation, they were checked every 15 min up to 60 min and then hourly until full maternal behavior was observed. Events observed after the first 30 min of continuous observation were recorded at the time of first observation (e.g., if full maternal behavior was first observed at 60 min, the full maternal behavior latency was scored as 60 min, or 3600 s). The same criterion was used for all other responses. For all behavioral tests, the observers were blind to the treatment of the test subjects.

Opioid-selective agonist treatment

Sixty virgin and lactating rats were randomly divided into two (experiment 1) and four (experiment 2) groups of 10 animals each. They were treated with U69593 (0.15 mg/kg), saline, or no treatment (i.e., no experimental procedures were conducted on these animals, which were defined as blank). Brains were collected on day 5 of lactation. After 1 h, the animals were decapitated for PAG dissection using a blade dissecting approximately 2 cm2 around the coordinate anteroposterior: 6.0; dorsoventral: 4.3; mediolateral: 0.6 coordinates (29). In both experiment, because the results for the saline and no treatment (blank) groups were similar (P > 0.5), they are presented as a single group (N = 10).

RNA extraction, cDNA construction, and real-time RT-PCR quantification of opioid gene expression

Total RNA was extracted from each tissue sample using TRIZOL reagent (Invitrogen Life Technologies, USA). Thus, immediately after euthanasia by decapitation, the PAG (approximately 40 mg, removed with a scalpel) was suspended in 1 mL ice-cold TRIZOL, and total RNA was extracted according to manufacturer instructions. The final RNA pellets were resuspended in 50 µL diethyl-pyrocarbonate-treated water. The total RNA concentrations were measured spectrophotometrically at 260 nm, and the integrity of RNA samples was analyzed on 1.5% agarose gel (Sigma, USA) containing ethidium bromide (0.5 µg/mL). Total RNA was then treated with DNase I before further processing and stored at -80°C.

Oligo DT primers (1 µL) and dNTPs (1 µL) were added to the total RNA sample (5 µg) and incubated at 65°C for 5 min; 5X buffer (4 µL; Superscript II RNase H-reverse transcriptase), DTT (1 M, 2 µL), and RNaseOUT (1 µL) were then added, and the mixture was incubated at 42°C for 2 min. Superscript II (1 µL) was added and the mixture was incubated at 42°C for 50 min. An additional incubation was performed at 70°C for 15 min. One microliter RNaseH was added for the removal of remaining RNA and the mixture was incubated at 37°C for 20 min. All reagents were purchased from Invitrogen Life Technologies.

Real-time RT-PCR was performed using an ABI Prism 7000 Sequence Detection System (Applied Biosystems, USA) with TaqMan Universal Master Mix (part No. 4304437; Applied Biosystems). PCR primers (Applied Biosystems) and the TaqMan probes for Oprm1, Oprd1, Oprk1, and 18S quantification were selected using the Primer Express software (Applied Biosystems), verified by a BLAST search of GenBank, and labeled Rn00565144_m1 for Oprm1, Rn00567737_m1 for Oprk1, RN00561699_m1 for Oprd1, and 4319413E for 18S, which was used as a housekeeping control. The primers were chosen to amplify a 65-bp fragment. The internal TaqMan probe (FAM-3’-TCTGGGCA CCTCTCTTT-5’-NFQ) was designed following the general rules outlined by the manufacturer and carried a 5’-reporter dye [6-carboxy fluorescein (FAM)] and a 3’-non-fluorescent quencher dye (NFQ). The primers and probes were used with 100% efficiency at final concentrations of 0.9 and 0.25 µM, respectively.

The thermal cycling conditions for cDNA quantification assays were established according to ABI Prism 7000 Sequence Detection System parameters. Relative gene expression data were analyzed by the 2-ΔΔCT method (30).

Statistical analysis

Behavioral data were analyzed by comparing the means using the Student t-test. The percents of animals showing each behavior during the 30-min test were compared by the Fisher test. Mean gene expression data were compared by the Student t-test. Values of P < 0.05 were considered to be statistically significant.


Results

Experiment 1

The 0.15 mg/kg dose of U69593 induced no sedation. Comparison of the saline and U69593 groups revealed that a lower percentage of U69593 group dams showed retrieval of first pup, and retrieving all pups, grouping, crouching and displaying full maternal behavior. Importantly, latencies to sniff the pups did not differ among groups (Table 1). Animals in the U69593 group continued digging in the wood chips and building nests instead of retrieving pups, resulting in longer latencies to retrieve the pups. Such disruptive effects were not observed in the saline group.

Experiment 2

Acute U69593 treatment significantly increased Oprk1 expression in virgin female rats (P < 0.05). This treatment did not induce alterations in Oprd1 or Oprm1 gene expression in the PAG of virgin female rats (Figure 1). In lactating female rats, U69593 treatment increased only Oprk1 expression (P < 0.01). No other significant differences were found in opioid receptor gene expression in lactating rats treated with this drug (Figure 1) in the PAG.


Figure 1. Real-time RT-PCR of 5 µg total RNA extracted from the periaqueductal gray of adult virgin (A, B, C) and lactating female rats (D, E, F) in relation to expression of Oprm1, Oprk1 and Oprd1. Data are reported as means ± SEM. *P < 0.05 compared to the blank group (ANOVA).

[View larger version of this image (54 K JPG file)]


Table 1. Effects of treatment with a selective agonist kappa-opioid receptor (U69593) on maternal behavior on day 5 of lactation.

[View larger version of this table (68 K JPG file)]


Discussion

The PAG belongs to a primary anatomical pathway mediating opioid-based analgesia. Morphine administration produces greater antinociception in males than females (31). In reproductive females, physiological activation of one or more PAG opioid receptors interferes with nursing and other aspects of maternal behavior, such as pup retrieval and pup grooming. The physiological role of female PAG opioid receptors, particularly the kappa receptor, has not been well established. The ventrolateral PAG column of the caudal part might be involved in the expression of kyphosis toward pups, which is the arched-back posture that facilitates nursing (17). Maternal aggression and survival strategies involving stressful situations have also been reported to be influenced by opioid receptors (16,17,32). A previous study reported that stimulation of kappa-opioid receptors using different doses of U69593 interferes with maternal behavior (8). Behavioral data reported in the present study show that peripheral injection of 0.15 mg/kg of the kappa agonist inhibits maternal behavior in lactating rats. On the other hand, other investigators administered a kappa 1 agonist (U69596, 0.1 mg/kg) and found no effect on maternal behavior in lactating rats. The larger dose used in the present study may be responsible for this difference. Alternatively, since another drug was used, kinetic differences may have played a role (33).

A previous study from our laboratory has reported the presence of kappa receptor protein in the PAG of both virgin and lactating rats (8). The present study investigated the expression of Oprm1, Oprk1, and Oprd1 in the PAG of female rats by evaluating the gene expression of mu-, kappa-, and delta-opioid receptors in the PAG of animals treated with an acute injection of U69593. The present data suggest that agonist-induced changes in gene expression are similar in both lactating and virgin animals. Treatment with a single peripheral injection of the kappa-opioid agonist U69593 significantly increased kappa receptor gene expression in both lactating and virgin rats. No significant changes were observed for mu or delta receptor genes after this drug challenge. Consistent with its binding affinity for kappa receptors, this action of U69593 on Oprk1 gene activity suggests a specificity of U69593 for actions on the gene encoding the kappa receptor. In the present study, the behavioral effects of acute kappa opioidergic stimulation in lactating rats were confirmed. In addition, the present data add knowledge to this scenario by demonstrating a specific effect of a kappa agonist on a site that has been functionally implicated in behavioral selection during lactation. Acute stimulation increased Oprk1 gene activity in both virgin and lactating animals. This may indicate a lack of endocrine modulation of this response. Thus, a specific immediate and likely compensatory gene response to kappa receptor stimulation is described in animals acutely exposed to a low dose of U69593. Such response may play a role in plastic mechanisms, resulting in different responses to similar pharmacological challenges. This hypothesis is to be tested in future studies.

The present study shows that by stimulating a kappa-opioid receptor both inhibition of maternal behavior and enhancement of Oprk1 are achieved. Although more studies are necessary to elucidate the functional relationship between these effects, a specific role for the kappa receptor in the context of reproductive behavior now seems feasible. This is yet another alert for the complex role of the opioid system in female reproduction.


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Acknowledgments

Research supported by FAPESP (#2010/50415-4) and CNPq grants to L.F. Felício (#478765/04-05) and E. Teodorov (#2004/54696-0).


Correspondence and Footnotes

Address for correspondence: L.F. Felício, Departamento de Patologia, FMVZ, USP, Av. Prof. Dr. Orlando M. de Paiva, 87, 05508-900 São Paulo, SP, Brasil. E-mail: lfelicio@usp.br

Received February 14, 2012. Accepted May 16, 2012. Available online June 1, 2012. Published September 3, 2012.


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