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Role of neuronal nitric oxide synthase (nNOS) at medulla in tachycardia induced by repeated administration of ethanol in conscious rats

Journal of Biomedical Science201825:8

https://doi.org/10.1186/s12929-018-0409-5

Received: 6 November 2017

Accepted: 15 January 2018

Published: 31 January 2018

Abstract

Background

Intake of ethanol (alcohol) has been shown to influence cardiovascular function; the underlying brain mechanism remains unclear. Noting that nitric oxide (NO) system in the CNS is involved in the regulation of cardiovascular function, the present study examined the role of NO in medulla in ethanol-induced cardiovascular changes.

Methods

Ethanol was administered by oral gavage at dose of 3.2 g/kg once every day for 8 consecutive days. Changes in blood pressure (BP) and heart rate (HR) in response to ethanol were measured by radiotelemetry method in freely moving female Sprague-Dawley rats. NO modulators were applied by intracerebroventricular (ICV) injection. The protein levels of nitric oxide synthase (NOS) and NO content in rostroventral medulla were measured by Western blot and nitrate/nitrite colorimetric assay kit, respectively.

Results

Ethanol intake had little effects on basal BP and HR following 8 consecutive day treatments. A significant increase in HR but not BP following ethanol intake was observed at 6th and 8th, but not at 1st and 4th day treatments as compared with saline group. A decrease in the protein expression of neuronal NOS (nNOS) but not inducible NOS or endothelial NOS and a decline in the level of NO in the medulla 30 min after ethanol administration was observed at 8th day treatment. ICV treatment with NO donors attenuated ethanol-induced tachycardia effects at 8th day treatment. Ethanol produced significantly tachycardia responses when ICV nNOS inhibitors were given at 1st day treatment.

Conclusion

Our results suggest that medulla nNOS/NO pathways play an important role in ethanol regulation of HR.

Keywords

EthanolHeart rateTachycardianNOSVentral medullaAutonomic nervous system

Background

The detrimental effects of ethanol undoubtedly are the major concern worldwide. To date, ethanol is the most abused drugs in the world and it affects major organs such as brain and heart. The effects of ethanol consumption can vary according to the amount of intake, exposure duration in terms of acute and chronic intake, and type of ethanol beverages such as beer and wine. Chronic low and moderate ethanol intake has been shown to be cardiovascular protective while chronic high intake of ethanol leads to high risk of cardiovascular disease [13]. Ethanol also may increase heart rate in human [4, 5] or animals [68]. However, the mechanism underlying this phenomenon is not well characterized. It has been reported that the effect of ethanol on central nervous system (CNS), particularly nuclei in ventral region of medulla contain neurons that are responsible for cardiovascular regulation [9, 10], plays a role in mediating changes in cardiovascular function [1116]. Thus, ethanol exposure may affect the function of the neurons in rostral ventrolateral medulla (RVLM) and the underlying cardiovascular regulation [17, 18].

Nitric oxide (NO) is a signaling molecule involved in neurotransmission within CNS as neuronal messenger [19]. NO is generated from amino acid L-arginine by the members of the NO synthase (NOS) family. There are three isoforms in the NOS family: neuronal NOS (nNOS), inducible NOS (iNOS) and endothelial NOS (eNOS) [20]. The three isoforms are localized differently in body’s organs. The constitute expression of iNOS isoform is low and induced under stress condition such as ischemia, trauma and inflammation [21, 22]. eNOS is mainly found in endothelial cells, vascular endothelium, and the smooth muscle. nNOS is a major isoform within the brain areas such as cerebral cortex, lateral dorsal, nucleus of solitary tract and cerebellum [23]. Previous studies have shown an increased vulnerability to ethanol-induced neuronal loss in the neocortex and hippocampus in neonatal mice genetically deficient for nNOS, suggesting a neuroprotective role of NO in ethanol intoxication [24]. In addition, central and peripheral NO and NOS have been demonstrated to participate in cardiovascular regulation [2528] and may play a cardioprotective role [29, 30].

Acute or chronic ethanol intake affects NOS activity; ethanol regulation of NOS activity may vary in different brain cells [31]. It is not clear whether ethanol regulation of NO signals in the CNS is involved in the cardiovascular effects of ethanol. The present study was undertaken to test the hypothesis that repeated ethanol intake may impair the regulation of cardiovascular function and NOS/NO system in the ventral medulla. Using an in vivo model, we demonstrated that repeated administration of ethanol caused tachycardia, which may be consequential to reduction of nNOS protein levels and NO level in ventral medulla of brain by ethanol.

Methods

Animals

All animal care and experimental protocols were carried out in accordance with the guidelines of the Institutional Animal Care and Use Committee of Tzu Chi University. Female Sprague-Dawley rats, aged 11–12 weeks were purchased from commercial supplier (BioLASCO Co., LTD., Taipei, Taiwan). The rats were housed and maintained in controlled room at 23 °C ± 1 °C, with 50% ± 10% humidity and a 12-h light/dark cycle. After radiotelemetry transmitter surgery with or without intracerebroventricular cannula implantation, the rats were housed individually in separated cages.

Determination of blood ethanol concentration

Blood ethanol concentrations were measured in another group of rats to avoid perturbing blood pressure and heart rate measurement. Prior to blood withdrawal, the rats were anesthetized using short-term inhalation anesthetic isoflurane (Panion & BF Biotech Inc., Taoyuan, Taiwan). The blood sample of 0.1 mL was withdrawn from the lateral tail vein using heparinized syringes at 30 min, 60 min, 120 min, and 180 min after oral gavage administration on day 1, day 3 and day 8. Blood ethanol levels were determined by an ethanol assay kit available commercially (BioAssay Systems, Hayward, CA); the rate of increase in absorbance at 580 nm was recorded with a microplate spectrophotometer (Epoch™, BioTek Instruments, Inc., Winooski, VT, USA).

Radiotelemetry transmitter surgery and blood pressure measurement

Under anesthetized by intraperitoneal injection of Zoletil (50 mg/kg), rats were implanted with the transmitter (model PAC40, Data Sciences International). A 4 to 5-cm-long midline incision through the skin and wall of abdomen was made. The location of abdominal aorta was uncovered by using sterile cotton swab. To allow access to the abdominal aorta, the intestine was retracted by using a sterile cotton pad pre-soaked with normal saline. Four to five-cm-long suture was passed to each caudal to the left renal vein and anterior to the iliac bifurcation. Tension was applied to both sutures to allow temporary blood flow occlusion. Using a bended tip of 22-gauge needle, aorta 1–2 mm anterior to the iliac bifurcation was pierced and the catheter was inserted quickly upstream toward the heart. The aorta entry site was dried by using sterile cotton tip applicators and a small amount of Tissue adhesive (Vetbond, 3 M Animal Care Products, St Paul, MN, USA) was used to secure the catheter. Both occlusion sutures were slowly released and removed. The transmitter was placed inside the cavity and sutured to the abdominal wall. The abdominal wall and skin were closed individually. Rats were allowed for recovery at least 7 days before used in the following experiment. After recovery periods, rats were placed individually on a receiver and the transmitter was turned on or turned off by using a magnet. The blood pressure and heart rate data were analyzed using Dataquest A.R.T. System 2.2 software for Windows (Data Sciences International). The data was processed and counted per 60 min before treatment and per 10 min after administration of ethanol.

Oral administration

Ethanol (3.2 g/kg, 40% v/v) or saline was given orally using 16-gauge 3-in.-long stainless steel needle (Cadence Science®, Cadence, Inc., Staunton, VA, USA). Before administration, the rats were restrained gently in upright position by grasping around the thorax to immobilize the head. The needle was inserted into the right side of the mouth and directed along the hard palate of the mouth to the back of the throat. Thereafter, the needle was passed into the esophagus until the base of the needle and ethanol or saline was delivered slowly.

Intracerebroventricular cannula implantation

Procedures for intracerebroventricular (ICV) cannula implantation were similar to those described previously [32]. Briefly, under anesthetized by intraperitoneal injection of Zoletil (50 mg/kg), rats were placed prone in a David Kopf stereotaxic frame and the head was fixed by ear bars and incisor bar. Occipital hole was drilled to the desired position in relation to the bregma using the following stereotaxic coordinates: 1.5 mm lateral to the midline, 0.8 mm caudal to the bregma. A stainless steel guide cannula (23-gauge) was placed into the hole, 3.5 mm below the dorsal surface of the brain and secured with two stainless steel screws and dental cement. A removable stylet was used to close the cannula. A 27-gauge stainless steel micropipette was connected to Hamilton microsyringes (10 μL) and used for ICV administration; drugs (3 μL) were injected using a syringe pump at a rate of 10 μL/min. The drinking behavior caused by ICV angiotensin II (50 ng, 5 μL) 3 days after surgery was used to determine correct placement of the guide cannula [33]; the rats that started drinking within 3 min after the injection were used for the following experiments.

Western blot analysis

The procedure for Western blot analysis of brain tissue was similar to that described in earlier studies [32, 34]. Rats were sacrificed 30 min after oral gavage of ethanol or saline. Brains were rapidly removed and soaked in ice-cold Krebs solution for 1 min. The brainstems were isolated from the brain and quickly frozen by cold spray (FREEZE 75; CRC Industry Europe NV, Zele, Belgium). Coronal section 0.5–1.5 mm rostral to the obex was prepared from the brainstem and the ventral part of the section was isolated. They were frozen in liquid nitrogen and stored at − 85 °C until used. About 10 mg of tissue was homogenized in 100 μL solution (0.32 M sucrose, 1 mM EDTA and 1 mTIU/ml aprotinin) with a homogenizer at speed of 10,000 rpm for 15 s. SDS was added to the sample to a final concentration of 0.1%, and 10 μg of protein was electrophoresed on 8% denaturing polyacrylamide gels. Separated proteins were transferred to PVDF transfer membrane and probed with primary antibody, rabbit anti-nNOS polyclonal antibody (1:1000, ab106417, Abcam, Cambridge, UK), rabbit anti-iNOS polyclonal antibody (1:1000, ab204017, Abcam, Cambridge, UK), and rabbit anti-eNOS polyclonal antibody (1:200, ab66127, Abcam, Cambridge, UK). Bound antibody was incubated with goat anti-rabbit secondary antibody (Bethyl, A120-101P, Bethyl Laboratories, Inc., Montgomery, TX, USA) conjugated to horseradish peroxidase which was reacted with Western Lighting® Plus-ECL Reagent (PerkinElmer, Waltham, MA, USA). The chemiluminescent signal was digitalized by UVP Biospectrum 810 (UVP, LLC, Upland, CA, USA) and the bands were analyzed with VisionWorks LS software for Windows (UVP, Upland). Protein concentrations were determined by BCA method (Sigma CO, St. Louis, MO, USA).

Determination of total nitrate-nitrite

The rats were sacrificed 30 min following saline or ethanol administration and rostroventral medulla was carefully dissected from the brain stem as experiments for Western blot. Total nitrate-nitrite levels were measured by nitrate-nitrite colorimetric assay kit (Cayman Chemical, Ann Arbor, MI, USA) based on Griess method, in which a chromophore with a strong absorbance at 545 nm was formed. NO values obtained by this method represent the total amount of nitrate and nitrite expressed in pmol/mg tissue.

Chemicals

Ethanol, NOC-18, and aprotinin were purchased from Sigma Co (St. Louis, Missouri, USA). NPLA was purchased from Tocris Cookson Ltd. (Bristol, UK). Zoletil® 50 was purchased from Virbac Taiwan Co. Ltd. (Taipei, Taiwan). Reagents for electrophoresis were purchased from Bio-Rad Laboratories (Richmond, CA).

Statistical analysis

Data were presented as mean±S.E.M. and were plotted and analyzed statistically with GraphPad Prism version 6.03 for Windows, GraphPad Software (La Jolla California USA). The time course of percentage changes in BP and HR after administration of ethanol or NO modulators was analyzed using repeated measure one-way ANOVA followed by Dunnett’s post-test. The results of BP, HR and blood ethanol concentration among various days of treatment and the effects of NOS modulators on ethanol effects at different times after administration were analyzed using repeated measure two-way ANOVA followed by the Bonferroni post-test. The results of Western blot analysis and total nitrate-nitrite were analyzed by unpaired t-test (comparison of two groups). P < 0.05 was considered statistically significant.

Results

Effects of ethanol on mean arterial pressure and heart rate

The values of basal mean arterial pressure (MAP) and heart rate (HR) were measured 1-h prior to ethanol or saline administration. Basal MAP and HR of saline group (n = 7) and ethanol group (n = 7) were 102.6 ± 2.0 mmHg and 347.0 ± 11.1 bpm and 101.0 ± 1.4 mmHg and 362.1 ± 6.4 bpm, respectively, in free moving, conscious female rats on day 1 administration. The values of MAP and HR were measured for 8 consecutive days. Compared to saline group, basal MAP and HR of ethanol group were similar in the course of 8 days (Fig. 1). Changes in blood ethanol concentrations of ethanol at 30 min, 60 min, 120 min and 180 min following intake of ethanol at 1st, 3rd, and 8th days of treatment are illustrated in Fig. 2. Blood ethanol concentrations were about 100 mg/dL and 60 mg/dL at 30 min and 180 min, respectively, after oral gavage of 3.2 g/kg ethanol. There is no statistical difference in xethanol blood levels during the observation period among various days of treatment. Oral gavage of saline caused increases in MAP and HR at the early period (10–30 min) after administration. Oral gavage of ethanol caused increases in MAP at the early period (10–20 min) while increases in HR during the observation period (Fig. 3). In comparison to saline group, ethanol did not cause a significant change in MAP over time after exposure on day 1 (Fig. 3a), day 4 (Fig. 3c), day 6 (Fig. 3e), and day 8 (Fig. 3g) treatments. Similarly, ethanol caused no change in HR during ethanol exposure on day 1 (Fig. 3b) and day 4 (Fig. 3d) treatments. However, ethanol produced significantly increases in HR on day 6 (Fig. 3f) and on day 8 (Fig. 3h) treatments as compared with saline group. The tachycardia occurred at 20–30 min after ethanol intake and lasted over 60 min.
Figure 1
Fig. 1

Bar graphs show basal MAP (top) and HR (bottom) before oral administration of 3.2 g/kg ethanol (n = 7) or saline (n = 7) at different days of treatment in freely moving rats. Ethanol (10 mL/kg, 40% (v/v)) or saline (10 mL/kg) was given by gavage once every day for 8 consecutive days. The values of MAP and HR represent an average value of 60 min recordings before ethanol or saline administration at each day of treatment

Figure 2
Fig. 2

Bar graphic shows changes in blood ethanol concentrations at different times after administration of ethanol at day 1, 3, and 8 treatments. Ethanol (3.2 g/kg) was administered once every day for 8 consecutive days (n = 4)

Figure 3
Fig. 3

Line graph show the time course of changes in MAP and HR after oral gavage of saline or ethanol at 1st (a, b), 4th (c, d), 6th (e, f), 8th (g, h) day treatment. Ethanol (10 mL/kg, 40% (v/v)) or saline (10 mL/kg) were administered once every day for 8 consecutive days (n = 7 each). The average BP and HR 60 min before ethanol administration are taken as baseline (B) of 100%. *P < 0.05 compared with baseline (B) using repeated measure one-way ANOVA followed by Dunnett’s post-test. #P < 0.05 compared with saline group analyzed by repeated measure two-way ANOVA followed by Bonferroni post-test

Effects of ethanol on the protein level of NOS and total amount of nitrate-nitrite in rostroventral medulla

The changes in the levels of NOS expressions in the rostroventral part of medulla 30 min after oral administration of saline or ethanol were estimated by immunological staining of Western blots with antibody against nNOS, iNOS, and eNOS. The results showed that the protein level of nNOS was significantly decreased, without significant changes in the levels of iNOS and eNOS compared with saline group at 8th day treatment. Representative Western blots and percentage changes in the levels of nNOS, iNOS, and eNOS protein content in the rostroventral medulla are shown in Fig. 4a, b, and c, respectively. To determine changes in the NO content, the total amount of nitrate and nitrite (NOx) in the rostroventral medulla were measured following administration of ethanol. The NOx levels at 30 min after administration were significantly decreased at day 8 treatment of ethanol (158.26 ± 10.86 pmol/mg) compared with saline group (309.19 ± 16.42 pmol/mg) (Fig. 4d).
Figure 4
Fig. 4

Bar graphs show Western blot analysis of the levels of nNOS (a), iNOS (b), eNOS (c) and changes in NOx (d) content in rostroventral medulla at 30 min after oral gavage of saline (10 mL/kg) or ethanol (3.2 g/kg) at day 8 treatment. Ethanol or saline was administered once every day for 8 consecutive days (n = 4 each). The ratio of different NOS to β-actin in saline group is taken as control of 100%. *P < 0.05 versus saline group analyzed using unpaired t-test

Effects of NO modulators on ethanol regulation of HR

ICV injection of NPLA (a nNOS inhibitor) alone in various dosages (up to 70 nmol) did not cause significant changes in MAP and HR over the observation period (Fig. 5a). However, ethanol produced a significant increases in HR but not MAP following ethanol intake in rats treated with ICV NPLA (10 nmol), which was applied immediately after oral gavage of ethanol, at day 1 ethanol treatment (Fig. 5b), suggesting that acute intake of ethanol may induce or potentiate the tachycardia effects while brain nNOS activity was impaired. ICV injection of a lower dose of NOC-18 (12 nmol, an NO donor) had little effects on MAP and HR. Higher doses of NOC-18 (60, 120 nmol) significantly reduced MAP and HR (Fig. 6a); the reduction lasted for about 20 min. Immediate ICV injection of low dose of NOC-18 (12 nmol) after ethanol administration reduced the tachycardia induced by ethanol at 8th day treatment; treatment with NOC-18 had no significant effects on BP responses (Fig. 6b).
Figure 5
Fig. 5

a Line graph shows the time course of percentage changes in MAP (left) and HR (right) after ICV injection of different doses of NPLA, a nNOS inhibitor (n = 4 each). The average BP and HR 60 min before NPLA injection are taken as baseline (b) of 100%. b Line graph show time course of percentage change in MAP (left) and HR (right) after administration of ethanol (3.2 g/kg) with or without ICV treatment with 10 nmol NPLA (n = 4) on day 1 treatment of ethanol. NPLA was given immediately after ethanol administration. The average BP and HR 60 min before ethanol administration are taken as baseline (b) of 100%. *P < 0.05 compared with baseline (b) using repeated measure one-way ANOVA followed by Dunnett’s post-test. #P < 0.05 compared with ethanol group analyzed by repeated measure two-way ANOVA followed by Bonferroni post-test

Figure 6
Fig. 6

a Line graph shows the time course of percentage changes in MAP (left) and HR (right) after ICV injection of different doses of NOC-18, an 00000NO donor (n = 3 each). The average BP and HR 60 min before NOC-18 injection are taken as baseline (b) of 100%. *p < 0.05 compared with baseline using repeated measure one way ANOVA followed by Dunnett’s posttests. b Line graph show time course of percentage change in MAP (left) and HR (right) after administration of ethanol with or without ICV treatment with 12 nmol NOC-18 (n = 4) on day 8 treatment of ethanol. NOC-18 was given immediately after ethanol administration. The average BP and HR 60 min before ethanol administration are taken as baseline (b) of 100%. #P < 0.05 compared with no ICV treatment using repeated measure two-way ANOVA followed by Bonferroni post-test

Discussion

In the present study, we showed that repeated daily administration of ethanol by oral gavage over 8 days did not significantly change the baseline BP and HR when compared to saline-treated rats. However, repeated ethanol intake caused a progressive increase in HR, but no significant changes in BP following ethanol administration. In addition, the protein level of nNOS and NO content decreased in rostroventral medulla after repeated administration of ethanol. We further showed that acute intake of ethanol produced tachycardia effects when brain nNOS activity was blocked by ICV nNOS inhibitors. ICV treatment with NO donor reduced the tachycardia induced by repeated administration of ethanol. Our results provide the first in vivo evidence that nNOS/NO system in the medulla of the brain participates in the regulation of HR by ethanol. The results imply that the central effects of ethanol play an important role in the mechanisms underlying ethanol regulation of cardiovascular function.

Central regulation of HR mainly relies on parasympathetic impulses from nucleus ambiguus (NA) and sympathetic impulses from RVLM. Both nuclei are located in ventral medulla oblongata. Parasympathetic stimulation has been known to slow down the HR; in contrast, sympathetic stimulation has been known to increase the HR. Ethanol has been repeatedly reported to increase HR [48] though the action mechanism is not well characterized. Some studies suggest that ethanol regulation of the activity of autonomic nuclei in the CNS plays a role in ethanol cardiovascular function. For instance, ethanol may inhibit pressor effects elicited by NMDA receptor stimulation in RVLM [17] or in contrast ethanol may induce pressor responses via the activation of NMDA receptors in the central nucleus of amygdala [11].

In the present study, ethanol did increase HR and BP following administration since day 1 treatment. Nevertheless, the increases in HR and BP existed in both ethanol group and saline group. This is reasonable because oral gavage administration of both ethanol and saline may impose stress on rats, leading to consequent increases in HR and BP. In line with our results, previous studies have shown that oral gavage caused a short-period increase in HR and BP [35]. On day 6 and 8 treatments, however, ethanol significantly increased HR after administration compared with saline group; the effects lasted for around 2-h observation period. The progressive increase in tachycardia responses to ethanol is not due to a baroreflex response because changes in MAP in both saline and ethanol groups are not statistically significant. The autonomic nervous system is crucial for regulation of BP and HR. Though BP and HR have close relationship each other, they are regulated by different mechanisms. Based on our findings, ethanol may have more effects on regulatory machinery of HR than that of BP. Our results showed a decrease in the protein levels and NO content in the rostroventral medulla during tachycardia responses after repeated daily ethanol intake. In addition, ICV application of NO modulators regulated ethanol-induced tachycardia effects. These results suggest that NO system in the autonomic nuclei in the CNS plays an important role in cardiovascular effects of ethanol. Moreover, ethanol-induced increases in HR after repeated administration were observed at blood concentrations of less than 100 mg/dL (0.1%) in the present study. Most heavy drinkers should reach this range of blood levels.

NO has been known as a key modulator in the brain and it has different effects on physiological function including cardiovascular function. Studies have shown that central endogenous and exogenous NO affects BP and HR [2529]. The role of NO in regulation of BP and HR may vary depending on its location and/or under influence of the other substances. For instance, decreases in nNOS protein expression and NO levels by overexpression of cystathionine-β synthase in the RVLM elicited increases in BP and HR in spontaneously hypertensive rats [36]. The mechanisms of superoxide-induced sympathoexcitation in hypertensive rats may partly involve the reduction of NO-mediated GABA release in the RVLM [37]. Those studies imply that increases in NO production in the RVLM may lower BP and HR. On the other hand, studies showed that nNOS-mediated NO production exhibited excitatory tonic activity in the RVLM [38, 39]. The cardioprotection role of nNOS/NO system has been noted in several studies such as control of baroreceptor reflex sensitivity [40], and maintenance of hemodynamic response during brain activation [41]. Our data showed that nNOS protein expression in rostroventral medulla of ethanol-treated rats was reduced on the 8th day treatment compared to saline-treated rats while iNOS and eNOS protein expression remained the same. This implies that the development of tachycardia following administration of ethanol during the course of treatment may be due to the reduction of nNOS protein expression in the rostroventral medulla. In accord with the changes in nNOS protein level, the level of NO represented by total nitrate/nitrite in rostroventral medulla was decreased on day 8 treatment 30 min following administration of ethanol. Previous in vitro and in vivo studies have shown that acute exposure of ethanol had little effects on NOS and nNOS enzyme activity in several brain areas [42, 43]. Thus the decreased NO level is most likely due to reduction in the protein expression of nNOS. Further work would be required to clarify the mechanism underlying ethanol-induced decrease in protein level of NOS.

The present study was carried out in conscious rats. ICV administration of agents regulating nNOS/NO system is the best choice to further clarify the role of nNOS/NO system in HR changes upon repeated ethanol exposure pharmacologically. We examined the effect of ICV nNOS inhibitors on the cardiovascular function. The results showed that neither BP nor HR was affected by ICV nNOS inhibitors alone. Nevertheless, microinjection of nNOS inhibitors into RVLM has been reported to result in significant hypotension and bradycardia [38, 39]. It is likely that nNOS inhibitors after ICV administration are widely diffused in the brain and thus the cardiovascular responses may result from the summation of the activation or inactivation of neuronal activity in various autonomic nuclei. However, treatment with ICV nNOS inhibitors leads to a notable increase in HR following acute administration of ethanol. Central NO donor is known to reduce BP and HR [28, 4446]. Similar to previous findings, our results showed that ICV NO donor can reduce BP and HR. These effects also can be seen when higher doses of NO donor were injected directly to RVLM [38]. Interestingly, our results showed attenuation of ethanol-tachycardia by ICV treatment with small dose of NO donor that has no effects on BP and HR though the attenuation only observed at early period after ethanol administration. The short-acting effect of NO donor may be due to rapid metabolism as our results showed that decreases in BP and HR following ICV administration of high doses of NO donor only lasted for a short period (10–20 min). By combining pharmacological and biochemical approaches, our results demonstrate the specific role of nNOS/NO system in the medulla in the tachycardia caused by repeated ethanol intake. Studies have documented the predominant role of NA, located in the ventral medulla, in regulation of HR [47]. Though our results are not able to indicate the exact site in the medulla due to the limitation of methodology (ICV administration of drugs), NA containing vagal cardioinhibitory neurons is the most likely site for ethanol regulation of HR because decreases in nNOS-mediated NO production may cause a reduction of neuronal activity in NA and a subsequent decrease in vagal tone, leading to tachycardia [48].

Ethanol concentration might be different in the brain among individual [49] and the effects of ethanol are highly correlated with its concentration in the blood. In our results, the blood ethanol concentration was not different between day 1 and day 8. This indicates that the effects of ethanol are not due to pharmacokinetic tolerance. The present study was carried out in female rats. It has been reported that ethanol reach peak concentration in the brain of female rats faster than male rats [50] and thus may cause worsen effect in female rats. In addition, it has been shown that acute ethanol-induced hypotensive effects in female rats are estrogen-dependent [51] . Additional experiments may be required to clarify the role of estrogen in HR responses during repeated administration of ethanol in female rats.

Conclusion

In conclusion, repeated daily ethanol intake that leads to a blood ethanol level comparable to a heavy drinker over 8 days induced tachycardia and decreased nNOS/NO system in the rostroventral medulla. Decreasing brain nNOS activity enhanced the development of tachycardia responses; and restoration of brain NO content could reduce the tachycardia responses. Thus nNOS/NO system in the medulla may play an important role in mediating ethanol-induced tachycardia during repeated ethanol exposure.

Abbreviations

BP: 

Blood pressure

CNS: 

Central nervous system

eNOS: 

Endothelial NOS

HR: 

Heart rate

ICV: 

Intracerebroventricular

iNOS: 

Inducible NOS

MAP: 

Mean arterial pressure

NA: 

Nucleus ambiguus

nNOS: 

Neuronal NOS

NO: 

Nitric oxide

NOS: 

Nitric oxide synthase

NOx: 

Nitrate and nitrite

RVLM: 

Rostral ventrolateral medulla

Declarations

Acknowledgements

Not applicable.

Funding

This study was supported by the Ministry of Science and Technology (MOST 103–2320-B-320 -003) and Tzu Chi University, Taiwan.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors’ contributions

JHS conducted the experiments, analyzed the data, participated in design experiments and drafted the manuscript. HHL and HL helped to perform the experiment. HHL participated in its design and contributed to the writing of the manuscript. CCL conceived of the study, wrote the manuscript and obtained funding. All authors approved the content of this manuscript.

Ethics approval and consent to participate

All experimental procedures were carried out in accordance with the protocol approved by the Institutional Animal Care and Use Committee of Tzu Chi University, Hualien, Taiwan. (protocol no. 102076).

Consent for publication

Yes, we consent for publication.

Competing interests

The authors declare that they have no competing interests.

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Authors’ Affiliations

(1)
Master and PhD Programs in Pharmacology and Toxicology, School of Medicine, Tzu Chi University, Hualien, Taiwan
(2)
Department of Physiology, School of Medicine, Tzu Chi University, Hualien, Taiwan
(3)
Department of Pharmacology, School of Medicine, Tzu Chi University, Hualien, Taiwan

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