Modulatory effect of three antibiotics on uterus bovine contractility
Transcription
Modulatory effect of three antibiotics on uterus bovine contractility
Theriogenology 82 (2014) 1287–1295 Contents lists available at ScienceDirect Theriogenology journal homepage: www.theriojournal.com Modulatory effect of three antibiotics on uterus bovine contractility in vitro and likely therapeutic approaches in reproduction M. Piccinno a, A. Rizzo a, M.A. Maselli b, M. Derosa c, R.L. Sciorsci a, * a Department of Emergency and Organ Transplantation, Section of Veterinary Medicine and Animal Production, University of Bari Aldo Moro, Valenzano Bari, Italy Experimental Pharmacology Laboratory, Scientific Institute of Gastroenterology IRCCS “S. de Bellis,” Castellana Grotte, Bari, Italy c ASL, Prefecture of Bari, Putignano, Bari, Italy b a r t i c l e i n f o a b s t r a c t Article history: Received 15 May 2014 Received in revised form 18 August 2014 Accepted 19 August 2014 This in vitro study investigates the modulatory effect of three antibiotics (amoxicillin, enrofloxacin, and rifaximin) on contractility of the bovine uterine tissue in follicular and luteal phases. The effects of these antibiotics at three single doses (106, 105, and 104 M) on their basal contractility were evaluated in isolated organ bath. The functionality of the strip throughout the experiment was evaluated by a dose of carbachol (105 M); the obtained effect had to be repeatable (difference of 20%) that is comparable to that induced by the previous administration of the same substance. The results demonstrate the different modulatory activities of these antibiotics on uterine contractility in follicular and luteal phases. The effects induced by amoxicillin and enrofloxacin are opposite: the first relaxes and the second increases the uterine contractility in both cycle phases. Instead, the activity of rifaximin varies depending on the phase of estrous cycle: it increases in the follicular phase and relaxes in the luteal phase. The obtained data provide the hypothesis of possible implications of these drugs in the pharmacologic modulation of uterine contractions. Their action at this level, associated with their specific antimicrobial effects, could suggest using these antibiotics for the treatment of diseases related to postpartum or infections that may occur in pregnant cattle, by virtue of their effects on myometrial contractility too. Ó 2014 Elsevier Inc. All rights reserved. Keywords: Amoxicillin Enrofloxacin Rifaximin Uterus contractility Bovine 1. Introduction The postpartum is a particularly critical period for bovine fertility, because of an increased susceptibility to recurrent infections of the uterus, which may give rise to chronic forms resulting in more or less prolonged infertility [1–3]. Several researches have been conducted on diseases that affect the uterus during delicate process of uterine involution [4–6]. In this period, the natural antibacterial mechanisms of the uterus (local production of antibodies, the phagocytic action of neutrophils and macrophages), the * Corresponding author. Tel.: þ39 0805443882; fax: þ39 0805443883. E-mail address: [email protected] (R.L. Sciorsci). 0093-691X/$ – see front matter Ó 2014 Elsevier Inc. All rights reserved. http://dx.doi.org/10.1016/j.theriogenology.2014.08.008 mechanical action of the secretions, and the contractile activity of myometrium [7–11] perform an action of selfcleaning by allowing, in most cases, to limit the duration and spread of infection [12]. However, sometimes the defense mechanisms are not able to counteract the action of bacteria [13,14], resulting in the development of pathologies, such as retained placenta and metritis, that affect the genital tract and the fertility of the subject [15,16]. These inflammatory processes may lead to a prolongation of the time needed to complete uterine involution and a delay in the resumption of ovarian activity [17,18]. The therapy of postpartum pathologies involves the local and systemic administration of antibiotics, alone or 1288 M. Piccinno et al. / Theriogenology 82 (2014) 1287–1295 associated with uterotonic substances [19–21]. The use of antibiotics was justified by their antimicrobial activity and for some of these (penicillins, quinolones, rifamycins, and macrolides) by their anti-inflammatory action and stimulatory effect on the immune system ([22–30]; M. Albrizio et al., unpublished data, 2014). Moreover, the antibiotics, such as penicillins and quinolones, can also affect the oxidative state of the organism and the production of reactive oxygen species [30–34]. Several studies have reported that antibiotic therapy is able to directly modulate the contractility of smooth muscles [35–39] also. However, this effect is subject to changes attributed to the species, tissue, or organ under examination [38–41]. For example, the erythromycin is able to stimulate the contraction of smooth muscle cells of the stomach and duodenum, probably by acting on the receptors of motilin [42,43] and moreover, seems to determine an increase in the amplitude and frequency of contraction even in rat’s myometrium; the effect probably mediated by histamine H1 receptors and calcium channels [44]. On the contrary, other studies have shown that erythromycin, as well as clarithromycin, neomycin, gentamicin, clindamycin, and ceftriaxone, would result in a relaxation of myometrial contractility in several species (woman, rat, and cow) [45–48]. Caron et al. [49] have also shown that the administration of amoxicillin and clavulanic acid determines, in humans, increased bowel activity, which could depend on the intraluminal release of mediators of contractility (e.g., motilin) or by direct interaction of the b-lactam with Gamma-AminoButyric Acid (GABA) receptors present at the level of the myenteric plexus. Other studies on smooth muscles of different organs and animal species have reported that fluoroquinolones act as antagonists of the GABA receptor by blocking the ATP-dependent potassium channels [36–38,41,50–52]. In addition, fluoroquinolones induce the release of PGF2a in guinea-pig ileum [38], which are responsible for cholinergic transmission in the myenteric plexus [53,54]. Moreover, in vitro studies on rat’s myometrium have reported that danofloxacin has a biphasic dose-related effect on uterine contractility induced by oxytocin. At low doses, the antibiotic induces an increase in the frequency and amplitude, thereby blocking ATP-dependant potassium channels, whereas at high doses, it decreases the peak area, probably blocking hyperpolarization [41]. In in vivo studies, there are conflicting opinions about the action of rifaximin on smooth muscles. Most authors believed that this antibiotic is not able to influence either the emptying rate or intestinal motility of mouse, rat, and human, except presence of small intestinal bacterial overgrowth [29,55,56]. On the basis of these premises, the aim of this work was to test the in vitro activity of amoxicillin, enrofloxacin, and rifaximin commonly used in bovine reproduction on the uterus contractility in this species. 2. Materials and methods 2.1. Uterine strip preparation A total of 68 uteri were obtained from cows slaughtered at a local abattoir. All uteri were found to be healthy and so were considered in our study: 33 from cows in the follicular phase and 35 from cows in the luteal phase. The estrus phase was recognized by antemortem and postmortem examinations. Antemortem, the phase of the estrous cycle and ovarian activity were determined through clinical examination, rectal palpation, and ultrasonography. At the same time, blood samples were collected from the coccygeal vein of each cow in prerefrigerated vacutainer glass tubes. After transporting blood samples to the laboratory, they were centrifuged at 1620 g for 10 minutes at 4 C. The sera were subsequently frozen at 20 C for later analysis of progesterone (P4), which was conducted with a competitive immunoenzymatic colorimetric method (Progesterone EIA WELL; Radim SpA, Pomezia [Roma], Italy). The crossreactions between P4 and steroid hormones were reported as follows: P4 100%; 11-a OH-P4 18%; 17-a OH-P4 16%; 20-a OH-P4 1%; estradiol less than 1 102%; testosterone less than 1 102%; cortisol less than 1 103%; and cholesterol less than 1 103%. The detection limit of the assay was 0.05 ng/mL. The intra-assay and interassay precisions had coefficient of variations of 2.9% and 4.8%, respectively. Cutoff values for estrus and diestrus were set at 1 ng/mL and greater than 2 ng/mL, respectively [57]. After stunning, the animals’ genital tract and functional ovarian structures were visually examined for further identification of the phase of the estrous cycle and to exclude any pathologic conditions [7]. The time from when the cows were slaughtered to when the uteri were collected was about 20 10 minutes. From each uterus, a single circular portion of the middle part of the ipsilateral horn to the functional ovarian structure was excised and immediately placed in a flask containing prerefrigerated and oxygenated Krebs solution (NaCl 113 mM, KCl 4.8 mM, CaCl2$2H2O 2.2 mM, MgSO4 1.2 mM, NaH2PO4 1.2 mM, NaHCO3 25 mM, glucose 5.5 mM, and sodium ascorbate 5.5 mM), which was prepared daily. The flask was then immediately transported to the laboratory in an insulated box. Mean transportation time was about 15 5 minutes. Uterine circular full-thickness portions were cut into strips (10 mm 3 mm) parallel to the longitudinal muscle fibers. 2.2. Experimental design The strips were immediately placed in an organ bath (10 mL) (model 4050; Ugo Basile, Milan, Italy) containing Krebs solution continuously bubbled with 95% O2 and 5% CO2. The pH was kept at 7.4, and the temperature was maintained at 37 C. A silk thread was used to tie the myometrial strips to an isometric transducer (FORT25; AD Instruments, Castle Hill, NSW, Australia). The contractile activities were recorded using a PowerLab 4/35 (AD Instruments acquisition software). After 1 hour, stabilization strips were placed under tension of 2 g for about 30 minutes. Next followed the equilibration, carbachol (105 M), the esterified form of acetylcholine, was added to the bath. This concentration of carbachol had a selective and prolonged contractant effect and was subsequently removed with the wash (washout). Carbachol was repeated after 30 minutes, time needed to ensure that the strip returned to the equilibrium condition. In the presence of a repeatable response M. Piccinno et al. / Theriogenology 82 (2014) 1287–1295 with a deviation of 20% or less, calculated by the formula (valuemaximum valueminimun/valuemaximum) 100, we proceeded to the experimental protocol, otherwise carbachol at the same concentration (105 M) was again administered (Fig. 1). If the latter administration of carbachol was not repeatable, the strip was discarded. The experimental protocol included those strips that were exposed to single concentrations of amoxicillin, enrofloxacin, and rifaximin (106, 105, and 104 M). Because there are no studies in this regard, the choice of concentrations used in vitro was made starting from the lowest concentration (106 M), and then ascending to reach in vitro concentrations that are closest to the minimum concentration of these antibiotics [58–60]. The rifaximin’s stock solution was made in ethanol, whereas those of amoxicillin and enrofloxacin were made in distilled water. Previous studies from our group reported that ethanol has no effect on in vitro uterine contractility of the cow [61]. The three antibiotics at concentrations of 106, 105, and 4 10 M were left in the bath for 10 minutes and then removed by washing. The time needed to obtain an effect of antibiotics on myometrial contractility was 10 minutes. Then, we proceeded to calculate the contractile activity as average amplitude (grams) and average frequency (number of contractions per minute), before and after the administration of antibiotics. For each concentration, the percentage increase from baseline was evaluated using the following formula: (T2 T1/T1) 100 [62]. 1289 2.4. Statistical analysis Amplitude and frequency values were expressed as the mean standard error of the mean (SEM) and were subjected to statistical analysis with SPSS Statistics 19 (IBM, New York, USA). Effects of different antibiotics in the two phases of the cycle and on the contractile response were analyzed with Student’s t test and one-way ANOVA and post hoc least significant difference test, respectively. The values were considered statistically significant at P < 0.05. 3. Results Spontaneous uterine contractility was observed in 27 strips of 33 uteri collected in the follicular phase and 32 strips of 35 uteri collected in the luteal phase. Nine strips that not show any spontaneous or comparable responses to carbachol (105 M) were discarded. The representative tracings (Figs. 2–4), respectively, show the effects induced by amoxicillin, enrofloxacin, and 2.3. Chemicals Carbachol, amoxicillin, and enrofloxacin were purchased from Sigma-Aldrich, Milano, Italy and rifaximin was a gift from Fatro, Italy. Other chemicals were obtained from commercial sources. Fig. 1. Representative tracing of the effect on uterine contractility induced by carbachol (105 M). The presence of two contractile responses comparable (difference of 20%) (confirmed) the functionality. The contraction evoked by carbachol was the control of our experiments and was always followed by its washout (w.o.). The amplitude (y-axis) is expressed in grams. Fig. 2. Representative tracing of the effects induced by the highest concentration of amoxicillin (104 M) in the follicular (A) and luteal (B) phases on uterine contractility. The amplitude (y-axis) is expressed in grams. 1290 M. Piccinno et al. / Theriogenology 82 (2014) 1287–1295 Fig. 4. Representative tracing of the effects induced by the highest concentration of rifaximin (104 M) in the follicular (A) and luteal (B) phases on uterine contractility. The amplitude (y-axis) is expressed in grams. Fig. 3. Representative tracing of the effects induced by the highest concentration of enrofloxacin (104 M) in the follicular (A) and luteal (B) phases on uterine contractility. The amplitude (y-axis) is expressed in grams. rifaximin at the highest concentration (104 M) tested in this study, in the follicular (Figs. 2A, 3A, and 4A) and luteal (Figs. 2B, 3B, and 4B) phases. The mean values SEM of amplitude and frequency before and after the administration of drugs (106, 105, and 104 M) and the relative percentage index are reported in Tables 1–6, respectively, for amoxicillin, enrofloxacin, and rifaximin. At all stages of the experiment, the amplitude and frequency of contraction baseline showed a statistically significant difference between the follicular and the luteal phases (Tables 1–6), as reported by previous work [63,64]. The contractile activity induced by the drugs tested was evaluated for a period of 10 minutes. This has allowed us to identify the effect and the real range of action of the molecules, which amounted to 2.5 and 9 minutes for amoxicillin, enrofloxacin, and rifaximin, respectively. The three antibiotics have modulated myometrial contractility in a different manner for activity and duration of action. In particular, amoxicillin had a concentrationdependent relaxing effect delayed in time, which was Table 1 Effect of single concentrations of amoxicillin on the amplitude contractions of bovine uterus contractions, during follicular and luteal phases. Amoxicillin (amplitude, g) Follicular phase Basal 106 M Basal 105 M Basal 104 M 1.70 1.66 1.65 1.60 1.76 1.62 Mean SEM 0.08c 0.07a 0.07c 0.07c 0.13a 0.09a Luteal phase Percentage index (%) Mean SEM L2.35 1.00 0.98 0.92 0.90 1.06 1.03 L3.03 L7.95 0.18d 0.19b 0.17d 0.15d 0.17b 0.18b Percentage index (%) L2.00 L2.17 L2.83 Data are expressed as the mean SEM. The table also shows, in bold, the percentage of decrease in the average amplitude of contraction of the myometrium bovine, after the administration of different concentrations of amoxicillin on basal value. In row superscripts a, b indicate P < 0.05 and c, d indicate P < 0.01. M. Piccinno et al. / Theriogenology 82 (2014) 1287–1295 1291 Table 2 Effect of single concentrations of amoxicillin on the frequency of contractions of bovine uterus, during follicular and luteal phases. Amoxicillin (frequency number of contractions/2.5 min) Follicular phase Basal 106 M Basal 105 M Basal 104 M 1.00 1.00 1.00 1.00 0.88 0.88 Mean SEM 0.13 0.13 0.14 0.17 0.15 0.19 Luteal phase Percentage index (%) Mean SEM 0 0.67 0.67 0.80 0.80 0.80 0.80 0 0 Percentage index (%) 0.08 0.13 0.13 0.13 0.12 0.12 0 0 0 Data are expressed as the mean SEM. The table also shows, in bold, the percentage index of the average frequency of bovine myometrium contraction, after the administration of different concentrations of amoxicillin on basal value. evident 1.5 minutes after the administration of the molecule, persisting for 2.5 minutes. The tonic effect induced by enrofloxacin began 1 minute after the administration and persisted for 3 minutes. This activity was present in both phases of the cycle (Fig. 3A, B). Even rifaximin had a delayed effect in time that occurred 1 minute after the administration and lasted until the wahout (9 minutes). This antibiotic determined a high and long-lasting contraction in the follicular phase (Fig. 4A), whereas in the luteal phase (Fig. 4B) it induced a massive and prolonged relaxation. Regarding the comparison between concentrations, statistically significant differences were observed only for the amplitude induced by rifaximin between 105 and 106 M in the follicular phase and between 104 and 106 M in the luteal phase, respectively (Table 5). The frequency induced by increasing the concentration of different antibiotics (106, 105, and 104 M) was not significantly different. The activity of antibiotics was also evaluated by the change in percentage index of contractility compared with its baseline. In both phases, amoxicillin caused a concentrationdependent decrease in the amplitude of contraction as shown by the percentages in Table 1. Such an effect was more evident in the follicular phase and, in particular, at a concentration of 104 M (7.95%). The frequency of contraction did not seem to be changed by amoxicillin (Table 2). Enrofloxacin had a tonic effect on myometrial contractility of the bovine species in both phases of the estrous cycle, with the highest values in the luteal phase (3.30%, 4.69%, and 6.77% at concentrations of 106, 105, and 104 M, respectively) (Table 3). Like amoxicillin, this antibiotic did not change the frequency of uterine contraction (Table 4). In the follicular phase, rifaximin determined an impressive and long-lasting increase in the contractile tone (12.45%, 21.25%, and 30.43% at concentrations of 106, 105, and 104 M, respectively), whereas in the luteal phase, it determined a relaxation of the strip by inducing a decrease in the contractile tone (26.34%, 34.97%, and 53.01% at concentrations of 106, 105, and 104 M, respectively) (Table 5). As regards with the frequency, rifaximin determined a decrease in the contractile tone in both phases with a greater decrease in the luteal phase at the concentration of 104 M (26.32%) (Table 6). 4. Discussion Uterine contractility is crucial for the realization of several reproductive events in both women and other mammals [65–67]. Understanding the mechanisms involved in myometrial contractility and their possible pharmacologic modulation is of great importance for the purpose of human obstetrics and gynecology and veterinary medicine. There are many studies that have evaluated the action of certain antibiotics (erythromycin, clarithromycin, neomycin, gentamicin, clindamycin, and ceftriaxone) on uterine contractility of woman, rat, and bovine, bringing a relaxing effect on myogenic activity and hormone induced [46–48,68]. These results support the hypothesis that antibiotics may act, in the postpartum, as a potential obstacle in the physiological process of self-cleaning, favoring the persistence of exudates and microorganisms inside the uterus. In our study, we tested for the first time the in vitro effect of three antibiotics (amoxicillin, enrofloxacin, and Table 3 Effect of single concentrations of enrofloxacin on the amplitude of contractions of bovine uterus, during follicular and luteal phases. Enrofloxacin (amplitude, g) Follicular phase Basal 106 M Basal 105 M Basal 104 M 2.04 2.05 2.07 2.13 2.00 2.12 Mean SEM 0.27a 0.28 0.18a 0.18a 0.23a 0.24a Luteal phase Percentage index (%) Mean SEM D0.49 1.21 1.25 1.28 1.34 1.33 1.42 D2.90 D6.00 0.21b 0.24 0.26b 0.26b 0.16b 0.16b Percentage index (%) D3.30 D4.69 D6.77 Data are the expressed as the mean SEM. The table also shows, in bold, the percentage of increase in the average amplitude of contraction of the myometrium bovine, after the administration of different concentrations of enrofloxacin on basal value. In row superscripts a, b indicate P < 0.05. 1292 M. Piccinno et al. / Theriogenology 82 (2014) 1287–1295 Table 4 Effect of single concentrations of enrofloxacin on the frequency of contractions of bovine uterus, during follicular and luteal phases. Enrofloxacin (frequencydnumber of contractions/3 min) Follicular phase Basal 106 M Basal 105 M Basal 104 M 1.33 1.33 1.20 1.20 1.25 1.25 Luteal phase Mean SEM 0.19a 0.19a 0.11a 0.12a 0.08c 0.05e Percentage index (%) Mean SEM 0 0.67 0.67 0.80 0.80 0.80 0.80 0 0 0.08b 0.13b 0.13b 0.13b 0.12d 0.12f Percentage index (%) 0 0 0 Data are expressed as the mean SEM. The table also shows, in bold, the percentage index of the average frequency of contraction of the myometrium bovine, after the administration of different concentrations of enrofloxacin on basal value. In row superscripts a, b indicate P < 0.05; c, d indicate P < 0.01; and e, f indicate P < 0.001. rifaximin), normally used in bovine reproduction, on the contractile activity of bovine uterus in the follicular and luteal phases. The results showed that all three antibiotics showed modulatory activity on uterine contractility, with the different effect and duration of action. In particular, the amoxicillin has induced a relaxing concentration-dependent effect on basal contractility in both phases of the cycle, with a more striking effect in the follicular phase. In this study, we have not studied the mechanism of action of the tested antibiotics; however, it is possible that the muscle relaxant effect may be attributed to amoxicillininduced stimulation of mechanisms involved in physiological uterine relaxation: activation of adenylate cyclase or the opening of potassium channels or to decreased levels of intracellular free calcium. The effect of amoxicillin on uterine contraction, associated with its antimicrobial effect highly selective for the bacterial wall, could suggest the using of this antibiotic for the treatment of diseases that may occur in pregnancy as it is not toxic to the embryo and fetus. Our analysis confirms that the amoxicillin could be used safely during pregnancy, as it may even assist and enhance the quiescence induced by P4 [69]. On the contrary, the use of the same antibiotic in the postpartum is counterproductive, as its effect on uterine contractility can negatively affect the self-cleaning. In our study, we also evaluated the effect exerted by enrofloxacin on uterus bovine contractility. This antibiotic has increased the spontaneous contractions of strips of bovine uterus in a concentrationdependent manner. In agreement with the previous studies of other fluoroquinolones [36,51], we believe that enrofloxacin acts even in the uterus such as GABAA antagonist, blocking the ATP-dependent potassium channels [36–38,41,50–52]. In support of this, the stimulatory action of enrofloxacin on uterine contractility, measured in our experiment, was higher in the luteal phase, the concentration of the GABAA receptor in uterine tissue [70]. On the contrary, the increased presence of GABAB receptors in the follicular phase [70] could explain the less effect of enrofloxacin on the uterine muscle measured by us at this stage of the cycle. In other studies conducted in the myenteric plexus, the ability of fluoroquinolones to stimulate the release of PGF2a that are responsible for releasing of acetylcholine at prejunctional cholinergic transmission and then inducing muscle contractility [53,71] too was reported. The excitatory effects on contractility highlighted in this study allow us to consider the possibility of using enrofloxacin in the therapy of retained placenta and endometritis in cattle, because in addition to the already known mechanisms of action, it may modulate the contractile activity facilitating cleaning and uterine involution. In particular, the use of this drug for the treatment of all forms of metritis, including chronic metritis, derives from the absence of a conditioning dictated by steroid hormones. It is possible that even in the uterus, as shown in the intestine [53,71], this could lead fluoroquinolones to induce the release of PGF2a, which are responsible of myometrial contractility and trigger the process of luteolysis, too. Regarding the rifaximin, its modulatory action on the contractility of the bovine uterus showed a twofold effect: in the follicular phase it increases tonic activity of uterus, Table 5 Effect of single concentrations of rifaximin on the amplitude of contractions, during follicular and luteal phases. Rifaximin (amplitude, g) Follicular phase Basal 106 M Basal 105 M Basal 104 M 2.49 2.80 2.87 3.48 2.30 3.00 Mean SEM 0.19a 0.22eB 0.15e 0.14eA 0.10a 0.13c Luteal phase Percentage index (%) Mean SEM D12.45 1.86 1.37 1.83 1.19 1.83 0.86 D21.35 D30.43 0.12b 0.11fB 0.12f 0.17f 0.11b 0.12dA Percentage index (%) L26.34 L34.97 L53.01 Data are expressed as the mean SEM. The table also shows, in bold, the percentage index of the average amplitude of contraction, after the administration of different concentrations of rifaximin on basal value. In row superscripts a, b indicate P < 0.05; c, d indicate P < 0.01; and e, f indicate P < 0.001. In column superscripts A, B indicate P < 0.05. M. Piccinno et al. / Theriogenology 82 (2014) 1287–1295 1293 Table 6 Effect of single concentrations of rifaximin on the frequency of contractions, during both cycle phases. Rifaximin (frequencydnumber of contractions/9 min) Follicular phase Basal 106 M Basal 105 M Basal 104 M 1.06 1.03 1.25 1.18 1.11 1.02 Luteal phase Mean SEM 0.15a 0.13a 0.10e 0.06e 0.05e 0.13c Percentage index (%) Mean SEM L2.83 0.64 0.58 0.50 0.40 0.57 0.42 L5.60 L8.11 Percentage index (%) 0.07b 0.11b 0.07f 0.11f 0.08f 0.09d L9.38 L20.00 L26.32 Data are expressed as the mean SEM. The table also shows, in bold, the percentage of decrease in the average frequency of contraction, after the administration of different concentrations of rifaximin, during the follicular and luteal phases. In row superscripts a, b indicate P < 0.05; c, d indicate P < 0.01; and e, f indicate P < 0.001. whereas in the luteal phase it induces a relaxation of the uterine musculature. From these results, it is conceivable that the effect induced by rifaximin is under the control of steroid hormones predominant at different stages of the cycle, respectively, estrogen in the follicular phase and P4 in the luteal phase. The in vitro studies that illustrate the action of this antibiotic on the smooth muscles are not present in the literature, whereas in vivo studies conflicting opinions are revealed. However, it is known that this molecule is able to bind to a nuclear receptor for steroids and xenobiotics [72–74]: the pregnane-X-receptor (PXR) [75,76] involved, in turn, in the modulation of myometrial contractility [77]. The binding of rifaximin with this receptor leads to an increased expression of PXR [75,76,78], but the synthesis of new receptors takes a long time [79], which is not covered by the timing of our laboratory procedures. However, in studies of the epithelial cells of the human colon knockout for PXR, Mencarelli et al. [78] found that rifaximin acted as an agonist of PXR too. Furthermore, Xue et al. [80] have clearly shown that the PXRs can suffer from coactivation of steroids and xenobiotics. In this sense, it is conceivable that in the presence of rifaximin, the PXRs might have sustained a hesitant coactivation potentiation of the contractant or releasing action exercised by the predominant steroid in the phase of the cycle in which it was the uterus (estrogen in the follicular phase and P4 in the luteal phase). In the light of what has been exposed, the increase in the contractile tone induced by the rifaximin under the influence of estrogen allows to consider the possibility of using this molecule at the time of heat, for the treatment of subacute metritis to facilitate the uterine cleaning. On the other hand, the relaxation obtained in the luteal phase, associated with the good selective toxicity given by substantial structural difference between the RNA polymerase of the prokaryotic cell and that of the eukaryotic cell [81,82], makes possible the use of rifaximin, if necessary, even during pregnancy as it intensifies uterine quiescence induced by P4. For this reason, its use is not suitable for the treatment of chronic metritis because the relaxing effect induced by rifaximin would favor the persistence of organic substances (liquid residues of childbirth, cellular debris, blood, pus) able to inactivate its own action. Further studies are, however, required to clarify the use of this antibiotic for the treatment of acute metritis, in which there is not a prevalent hormonal state, as the disease is realized before the functional reactivation of reproductive axis. 4.1. Conclusions This study shows, for the first time, the modulatory activity of three antibiotics (amoxicillin, enrofloxacin, and rifaximin) on the bovine uterine contractility. The drugs tested show different effects that allow to ascribe their therapeutic use in accordance with their ability to modulate uterine contractility (Table 7) too. From a clinical point of view, our study provides, for the three antibiotics tested, a starting point for new directions in the field of bovine reproduction. The inhibitory effect of amoxicillin on uterus contractility supports the hypothesis that this drug can be used in therapy of infectious diseases Table 7 Therapeutic indications and incorrect use of antibiotics tested in this study, according to their ability to modulate uterine contractility. Antibiotic Therapeutic indications Do not use in case of Class Molecules Period of use Diseases Period of use Diseases B-lactams Amoxicillin Pregnancy Postpartum Retained placenta Metritis postpartum Rifamycin Rifaximin Pregnancy 40–60 days postpartum Chronic metritis Fluoroquinolones Enrofloxacin 14–40 days postpartum Postpartum Pregnancy Each type of pathology Mastitis Respiratory system Digestive system Urinary tract Skin and soft tissue Mastitis Digestive system Subacute metritis Metritis postpartum 1294 M. Piccinno et al. / Theriogenology 82 (2014) 1287–1295 in the course of pregnancy. To this end, it is possible that the use of rifaximin under the influence of P4 is able to determine a lasting uterus relaxation. The role of this antibiotic, however, is twofold; if used in the presence of estrogen, rifaximin may stimulate high contraction that could justify its use during the heat for the treatment of subacute metritis to facilitate the uterine cleaning. On the contrary, enrofloxacin is not affected by hormonal changes; this would encourage the use of this drug for the treatment of all forms of metritis, including chronic metritis; thanks to the ability of this fluoroquinolone to induce the release of PGF2a as well. Further studies are, however, needed to evaluate the mechanism of action of the antibiotics tested and evaluate their effect in combination with ecbolic substances normally used in the postpartum dairy cows. [18] [19] [20] [21] [22] [23] [24] Acknowledgments [25] Fatro, pharmaceutical industry, for supplying products used in this research. [26] References [1] Minoia P, Sciorsci RL. Problemi etiopatogenetici, prognostici e terapeutici di alcune affezioni genitali dei bovini. In: Minoia P, editor. Problematiche di Biologia, Fisiopatologia e Clinica della Riproduzione Animale. Bari: Quadrifoglio; 1988. [2] Sheldon IM, Dobson H. Postpartum uterine health in cattle. Review. Anim Reprod Sci 2004;82–83:295–306. [3] Pantaleo M, Rizzo A, D’Onghia G, D’Onghia G, Roncetti M, Piccinno M, et al. Immunological aspects of metritis in dairy cows: a review. Endocrin Metab Immune Disord Drug Targets 2014;14. [4] Robbe D, Lacalandra G, Zarrilli A, Campanella F, Sciorsci RL. Livelli di idrossiprolina serica e monitoraggio clinico dell’involuzione uterina in bovine trattate con Naloxone e Calcio - ATTI S.I.B. 1999;31: 231– 237. [5] Lograno MD, Romano MR, Cosola C, Minoia R, Rizzo A, Sciorsci RL. Isometric modulation of bovine uterine strips, effect of GnRH (lecirelin). Obiettivi Doc Vet 2004;25:21–4. [6] Minoia G, Trisolini C, De Sandro Salvati A, De Palma A, Minoia R, Rizzo A, et al. Gestione aziendale ed ipofertilità nella bovina da latte. Obiettivi Doc Vet 2004;25:7–12. [7] Arthur GH. Veterinary reproduction and obstetric. London: Saunders; 2001. [8] Akira S, Uematsu S, Takeuchi O. Pathogen recognition and innate immunity. Cell 2006;124:783–801. [9] Bajcsy AC, Szenci O, Van der Weijden GC, Doornenbal A, Maassen F, Bartyik J, et al. The effect of a single oxytocin or carbetocin treatment on uterine contractility in early postpartum dairy cows. Theriogenology 2006;65:400–14. [10] O’Neill LA. The interleukin-1 receptor/toll-like receptor superfamily: 10 years of progress. Immunol Rev 2008;226:10–8. [11] LeBlanc SJ, Osawa T, Dubuc J. Reproductive tract defense and disease in postpartum dairy cows. Theriogenology 2011;76:1610–8. [12] Sali G. Materiale di teriogenologia bovina. Bologna: Edagricole; 1996. [13] Zwald NR, Weigel KA, Chang YM, Welper RD, Clay JS. Genetic selection for health traits using producer-recorded data. I. Incidence rates, heritability estimates, and sire breeding values. J Dairy Sci 2004;87:4287–94. [14] Martinez N, Risco CA, Lima FS, Bisinotto RS, Greco LF, Ribeiro ES, et al. Evaluation of peripartal calcium status, energetic profile, and neutrophil function in dairy cows at low or high risk of developing uterine disease. J Dairy Sci 2012;95:7158–72. [15] Ross JD. An update on pelvic inflammatory disease. Sex Transm Infect 2002;78:18–9. [16] Sheldon IM, Lewis GS, LeBlanc S, Gilbert RO. Defining postpartum uterine disease in cattle. Theriogenology 2006;65:1516–30. [17] Risco CA, Drost M, Thatcher WW, Savio J, Thatcher MJ. Effects of calving-related disorders on prostaglandin, calcium, ovarian activity [27] [28] [29] [30] [31] [32] [33] [34] [35] [36] [37] [38] [39] [40] [41] and uterine involution in postpartum dairy cows. Theriogenology 1994;42:183–203. LeBlanc SJ, Duffield TF, Leslie KE, Bateman KG, Keefe GP, Walton JS, et al. Defining and diagnosing postpartum clinical endometritis and its impact on reproductive performance in dairy cows. J Dairy Sci 2002;85:2223–36. Földi J, Kulcsár M, Pécsi A, Huyghe B, de Sa C, Lohuis JA, et al. Bacterial complications of postpartum uterine involution in cattle. Anim Reprod Sci 2006;96:265–81. Beagley JC, Whitman KJ, Baptiste KE, Scherzer J. Physiology and treatment of retained fetal membranes in cattle. J Vet Intern Med 2010;24:261–8. Gnemmi G. Patologie uterine di interesse clinico. In: Sali G, editor. Gestione clinica della riproduzione bovina. Milano, Italia: Le Point Vétérinatre Italie srl; 2013. p. 121–50. Roche Y, Gougerot-Pocidalo MA, Fay M, Etienne D, Forest N, Pocidalo JJ. Comparative effects of quinolones on human mononuclear leucocyte functions. J Antimicrob Chemother 1987;19:781–90. Korzeniowski OM. Effects of antibiotics on the mammalian immune system. Infect Dis Clin North Am 1989;3:469–78. Takeshita K, Yamagishi I, Harada M, Otomo S, Nakagawa T, Mizushima Y. Immunological and anti-inflammatory effects of clarithromycin: inhibition of interleukin 1 production of murine peritoneal macrophages. Drugs Exp Clin Res 1989;15:527–33. Iino Y, Toriyama M, Natori K, You A. Erythromycin inhibition of lipopolysaccharide-stimulated tumor necrosis factor alpha production by human monocytes in vitro. Ann Otol Rhinol Laryngol Suppl 1992;157:16–20. Morikawa K, Oseko F, Morikawa S, Iwamoto K. Immunomodulatory effects of three macrolides, midecamycin acetate, josamycin, and clarithromycin, on human T-lymphocyte function in vitro. Antimicrob Agents Chemother 1994;38:2643–7. Morikawa K, Watabe H, Araake M, Morikawa S. Modulatory effects of antibiotics on cytokine production by human monocytes in vitro. Antimicrob Agents Chemother 1996;40:1366–70. Van Vlem B, Vanholder R, De Paepe P, Vogelaers D, Ringoir S. Immunomodulating effects of antibiotics: literature review. Infection 1996;24:275–91. Scarpignato C, Pelosini I. Rifaximin, a poorly absorbed antibiotic: pharmacology and clinical potential. Chemotherapy 2005;51:36–66. Rizzo A, Pantaleo M, Mutinati M, Trisolini C, Minoia G, Spedicato M, et al. Effects of antibiotics on biochemical parameters, leucocytes and reactive oxygen species (ROS) in bitches after ovariectomy. Immunopharmacol Immunotoxicol 2009;31:682–7. Gunther MR, Mao J, Cohen MS. Oxidant-scavenging activities of ampicillin and sulbactam and their effects on neutrophil function. Antimicrob Agents Chemother 1993;37:950–6. Hoeben D, Burvenich C, Heyneman R. Influence of antimicrobial agents on bactericidal activity of bovine milk polymorphonuclear leukocytes. Vet Immunol Immunopathol 1997;56:271–82. Gürbay A, Gonthier B, Daveloose D, Favier A, Hincal F. Microsomal metabolism of ciprofloxacin generates free radicals. Free Radic Biol Med 2001;30:1118–21. Mutinati M, Spedicato M, Manca R, Trisolini C, Minoia G, Rizzo A, et al. Influence of antibiotic therapy on serum levels of reactive oxygen species in ovariectomized bitches. J Vet Pharmacol Ther 2008;31:18–21. Paradelis AG, Tarlatzis BC, Triantaphyllidis CJ, El-Messidi MM, Papaloucas AC. Effect of aminoglycoside antibiotics on the contractility of the uterus. Methods Find Exp Clin Pharmacol 1982; 4:337–41. Ito K, Murakami K, Tamura K. Alpha 1-adrenoceptor-blocking activity of ofloxacin and ciprofloxacin in isolated vascular smooth muscles. Arch Int Pharmacodyn Ther 1993;325:86–95. Tagaya E, Tamaoki J, Takemura H, Chiyotani A, Konno K. Effect of ciprofloxacin on contractile responses of canine airway smooth muscle. Kansenshogaku Zasshi 1995;69:404–7. Di Nucci A, Candura SM, Tagliani M, D’Agostino G, Spelta V, Fiori E, et al. Fluoroquinolone-induced motor changes in the guinea-pig isolated ileum. Pharmacol Toxicol 1998;83:263–9. Granovsky-Grisaru S, Ilan D, Grisaru D, Lavie O, Aboulafia I, Diamant YZ, et al. Effect of erythromycin on contractility of isolated myometrium from pregnant rats. Am J Obstet Gynecol 1998;178(1 Pt. 1):171–4. Celik H, Ayar A, Sapmaz E. Effects of erythromycin on stretchinduced contractile activity of isolated myometrium from pregnant women. Acta Obstet Gynecol Scand 2001;80:697–701. Akar Y, Kara H, Servi K, Yildiz H. The effect of danofloxacine on in vitro rat myometrium. Pak Vet J 2010;30:211–4. M. Piccinno et al. / Theriogenology 82 (2014) 1287–1295 [42] Peeters T, Matthijs G, Depoortere I, Cachet T, Hoogmartens J, Vantrappen G. Erythromycin is a motilin receptor agonist. Am J Physiol 1989;257(3 Pt. 1):G470–4. [43] Collard JM, Romagnoli R, Otte JB, Kestens PJ. Erythromycin enhances early postoperative contractility of the denervated whole stomach as an esophageal substitute. Ann Surg 1999;229:337–43. [44] Liu H, Zhu T, Ma Y, Qu S. Effect of erythromycin on contractile response of uterine smooth muscle strips in non-pregnant rats. Pol J Pharmacol 2003;55:57–62. [45] Phillippe M. Neomycin inhibition of hormone-stimulate smooth muscle contractions in myometrial tissue. Biochem Biophys Res Commun 1994;205:245–50. [46] Celik H, Ayar A. Clarithromycin inhibits myometrial contractions in isolated human myometrium independent of stimulus. Physiol Res 2002;51:239–45. [47] Ocal H, Yuksel M, Ayar A. Effects of gentamicin sulfate on the contractility of myometrium isolated from non-pregnant cows. Anim Reprod Sci 2004;84:269–77. [48] Elsayed M, Elkomy A, Aboubakr MH. Ceftriaxone reduces contractility of isolated uterine smooth muscles of pregnant and nonpregnant rat. Res J Pharmacol 2011;5:31–4. [49] Caron F, Ducrotte P, Lerebours E, Colin R, Humbert G, Denis P. Effects of amoxicillin-clavulanate combination on the motility of the small intestine in human beings. Antimicrob Agents Chemother 1991;35: 1085–8. [50] Anderson ME, Mazur A, Yang T, Roden DM. Potassium current antagonist properties and proarrhythmic consequences of quinolone antibiotics. J Pharmacol Exp Ther 2001;296:806–10. [51] Becker B, Antoine M-H, Nguyen QA, Rigo B, Cosgrove KE, Barnes PD, et al. Synthesis and characterization of a quinolinonic compound activating ATP-sensitive Kþ channels in endocrine and smooth muscle tissues. Br J Pharmacol 2001;134:375–85. [52] Zünkler BJ, Woss M. Effect of lomefloxacin and norfloxacin on pancreatic B-cell ATP sensitive Kþ channels. Life Sci 2003;73:429–35. [53] Serio R, Daniel EE. Eicosanoids and peripheral neurotransmission. Prostaglandins Leukot Essent Fatty Acids 1989;38:237–46. [54] Takeuchi T, Okuda M, Yagasaki O. The differential contribution of endogenous prostaglandins to the release of acetylcholine from the myenteric plexus of the guinea-pig ileum. Br J Pharmacol 1991;102: 381–5. [55] Dayan AD. Rifaximin (NormixÒ). Preclinical Expert Report. London; 1997. [56] Husebye E. The pathogenesis of gastrointestinal bacterial overgrowth. Chemotherapy 2005;51(Suppl. 1):1–22. [57] Hirsbrunner G, Knutti B, Liu I, Küpfer U, Scholtysik G, Steiner A. An in vitro study on spontaneous myometrial contractility in the cow during estrus and diestrus. Anim Reprod Sci 2002;70:171–80. [58] Andes D, Craig WA. In vivo activities of amoxicillin and amoxicillinclavulanate against Streptococcus pneumoniae: application to breakpoint determinations. Antimicrob Agents Chemother 1998;42: 2375–9. [59] Nuermberger E, Grosset J. Pharmacokinetic and pharmacodynamic issues in the treatment of mycobacterial infections. Eur J Clin Microbiol Infect Dis 2004;23:243–55. [60] Davis JL, Foster DM, Papich MG. Pharmacokinetics and tissue distribution of enrofloxacin and its active metabolite ciprofloxacin in calves. J Vet Pharmacol Ther 2007;30:564–71. [61] Rizzo A, Cosola C, Mutinati M, Spedicato M, Minoia G, Sciorsci RL. Bovine ovarian follicular cysts: in vitro effects of lecirelin a GnRH analogue. Theriogenology 2010;74:1559–69. [62] Piccinno M, Zupa R, Corriero A, Centoducati G, Passantino L, Rizzo A, et al. In vitro effect of isotocin on ovarian tunica albuginea [63] [64] [65] [66] [67] [68] [69] [70] [71] [72] [73] [74] [75] [76] [77] [78] [79] [80] [81] [82] 1295 contractility of gilthead seabream (Sparus aurata L.) in different reproductive conditions. Fish Physiol Biochem 2014;40:1191–9. Rizzo A, Spedicato M, Cosola C, Minoia G, Roscino MT, Punzi S, et al. Effects of rosiglitazone, a PPAR-gamma agonist, on the contractility of bovine uterus in vitro. J Vet Pharmacol Ther 2009;32:548–51. Rizzo A, Angioni S, Spedicato M, Minoia G, Mutinati M, Trisolini C, et al. Uterine contractility is strongly influenced by steroids and glucose metabolism: an in vitro study on bovine myometrium. Gynecol Endocrinol 2011;27:636–40. Kündig H, Thun R, Zerobin K, Bachmann B. The uterine motility of cattle during late pregnancy, labor and puerperium. I. Spontaneous motility. Schweiz Arch Tierheilkd 1990;132:77–84. Slama H, Vaillancourt D, Goff AK. Pathophysiology of the puerperal period: relationship between prostaglandin E2 (PGE2) and uterine involution in the cow. Theriogenology 1991;36:1071–90. Fanchin R, Picone O, Ayoubi JM, Marcadet-Fredet S, Kadoch J, Frydman R. Uterine contractility and reproduction: new perspectives. J Gynecol Obstet Biol Reprod 2002;31:325–32. Kadanali S, Demir N, Apaydin S. In vitro relaxant effects of gentamycin and clyndamicin on human myometrium at term. A preliminary study. New J Med 1996;13:75–8. Leonhardt SA, Edwards DP. Mechanism of action of progesterone antagonists. Exp Biol Med (Maywood) 2002;227:969–80. Majewska MD, Vaupel DB. Steroid control of uterine motility via gamma-aminobutyric acid A receptors in the rabbit: a novel mechanism? J Endocrinol 1991;131:427–34. Mulholland MW, Simeone DM. Prostaglandin E2 stimulation of acetylcholine release from guinea pig myenteric plexus neurons. Am J Surg 1993;166:552–6. Kliewer SA, Goodwin B, Willson TM. The nuclear pregnane X receptor: a key regulator of xenobiotic metabolism. Endocr Rev 2002;23:687–702. Sonoda J, Rosenfeld JM, Xu L, Evans RM, Xie W. A nuclear receptormediated xenobiotic response and its implication in drug metabolism and host protection. Curr Drug Metab 2003;4:59–72. Sonoda J, Chong LW, Downes M, Barish GD, Coulter S, Liddle C, et al. Pregnane X receptor prevents hepatorenal toxicity from cholesterol metabolites. Proc Natl Acad Sci U S A 2005;102:2198–203. McKay LI, Cidlowski JA. Molecular control of immune/inflammatory responses: interactions between nuclear factor-kappa B and steroid receptor-signaling pathways. Endocr Rev 1999;20:435–59. Arrese M, Karpen SJ. Nuclear receptors, inflammation, and liver disease: insights for cholestatic and fatty liver diseases. Clin Pharmacol Ther 2010;87:473–8. Mitchell BF, Mitchell JM, Chowdhury J, Tougas M, Engelen SM, Senff N, et al. Metabolites of progesterone and the pregnane X receptor: a novel pathway regulating uterine contractility in pregnancy? Am J Obstet Gynecol 2005;192:1304–13. Mencarelli A, Migliorati M, Barbanti M, Cipriani S, Palladino G, Distrutti E, et al. Pregnane-X-receptor mediates the antiinflammatory activities of rifaximin on detoxification pathways in intestinal epithelial cells. Biochem Pharmacol 2010;80:1700–7. Chechik G, Koller D. Timing of gene expression responses to environmental changes. J Comput Biol 2009;16:279–90. http://dx.doi. org/10.1089/cmb.2008.13TT. Xue Y, Moore LB, Orans J, Peng L, Bencharit S, Kliewer SA, et al. Crystal structure of the pregnane X receptor-estradiol complex provides insights into endobiotic recognition. Mol Endocrinol 2007; 21:1028–38. Wehrli W, Staehelin M. Actions of the rifamycins. Bacteriol Rev 1971;35:290–309. Adachi JA, DuPont HL. Rifaximin: a novel nonabsorbed rifamycin for gastrointestinal disorders. Clin Infect Dis 2006;42:541–7.