Low heritability in pharmacokinetics of talinolol: a pharmacogenetic twin study on the heritability of the pharmacokinetics of talinolol, a putative probe drug of MDR1 and other membrane transporters

Background Efflux transporters like MDR1 and MRP2 may modulate the pharmacokinetics of about 50 % of all drugs. It is currently unknown how much of the variation in the activities of important drug membrane transporters like MDR1 or MRP2 is determined by genetic or by environmental factors. In this study we assessed the heritability of the pharmacokinetics of talinolol as a putative probe drug for MDR1 and possibly other membrane transporters. Methods Talinolol pharmacokinetics were investigated in a repeated dose study in 42 monozygotic and 13 same-sex dizygotic twin pairs. The oral clearance of talinolol was predefined as the primary parameter. Heritability was analyzed by structural equation modeling and by within- and between-subject variance and talinolol clearance was correlated with polymorphisms in MDR1, MRP2, BCRP, MDR5, OATP1B1, and OCT1. Results Talinolol clearance varied approximately ninefold in the studied sample of healthy volunteers. The correlation of clearances between siblings was not significantly different for the monozygotic and dizygotic pairs. All data analyses consistently showed that variation of talinolol pharmacokinetics was mainly determined by environmental effects. Structural equation modeling attributed 53.5 % of the variation of oral clearance to common environmental effects influencing both siblings to the same extent and 46.5 % to unique environmental effects randomly affecting individual subjects. Talinolol pharmacokinetics were significantly dependent on sex, body mass index, total protein consumption, and vegetable consumption. Conclusions The twin study revealed that environmental factors explained much more of the variation in pharmacokinetics of talinolol than genetic factors. Trial registration European clinical trials database number: EUDRA-CT 2008-006223-31. Registered 26 September 2008. ﻿ClinicalTrials.gov number: NCT01845194. Electronic supplementary material The online version of this article (doi:10.1186/s13073-016-0372-2) contains supplementary material, which is available to authorized users.


Background
Efflux transmembrane transport of drugs and other molecules is highly variable within and between humans due to inherited and environmental factors. This can have profound consequences for the intended and adverse effects of drugs and for the biological effects of many other endogenous and exogenous molecules. Efflux transporters first came into focus as mediators of multi-drug resistance in cancer chemotherapy [1,2]. Among the efflux transporters, multi-drug resistance protein 1 (MDR1, P-glycoprotein), encoded by the ABCB1 gene, has been the most extensively studied [3][4][5][6][7][8][9]. MDR1 is expressed on the apical membrane of enterocytes, hepatocytes, and renal tubular cells and at the bloodbrain barrier and the blood-testes barrier and protects cells and organs against overload with numerous substances [10,11]. Some animals completely lack MDR1 but we do not know of any humans completely lacking it [10]. Nevertheless, MDR1 expression and activity vary substantially between individuals. MDR1 expression is regulated by several mechanisms and substantial up-regulation can be induced by several substances and is mediated by PXR, RXR, and other nuclear transcription factors [12]. On the other hand, numerous environmental substances and drugs, such as cyclosporine or verapamil, can substantially inhibit P-glycoprotein [13,14].
Inherited polymorphisms may contribute to variation in MDR1 activity. In particular, the polymorphisms C1236T (silent), G2677T/A (Ala893Ser/Thr), and C3435T (silent) have been extensively studied [15][16][17][18][19][20][21][22][23][24]. Understanding of the functional role of these variants in humans is complicated by the fact that these variants are in strong linkage disequilibrium [25,26]. Genetic polymorphisms may play some role in the variation of MDR1 expression and activity. However, the genotype-phenotype correlation data obtained by different investigators is not entirely consistent. In conclusion, it is currently unknown how much of the variation in MDR1 activity as tested in vivo with putative probe drugs like talinolol or digoxin is explained by environmental or heritable factors.
Another efflux transporter of particular interest for the disposition of drugs, other foreign compounds, and endogenous substrates is the multidrug resistance-associated protein 2 (MRP2; also known as ABCC2 (ATP binding cassette subfamily C member 2)). MRP2 is expressed in a broad range of tissues and also contributes to multidrug resistance in cancer therapy [27]. It is expressed on the apical membrane of cells in the liver, intestine, and kidneys [28,29]. MRP2 is an important efflux transporter of conjugated bilirubin and inherited lack of activity is known as Dubin-Johnson syndrome [30]. Furthermore, MRP2-mediated drug interactions may cause liver toxicity [31]. Activity of MRP2 can also be greatly modified by transcriptional regulation and by inhibition of its transport function, but also by genetic polymorphisms. Among others, the impact of two genetic polymorphisms (-C24T and G1249A in MRP2) on, for example, the bioavailability of mycophenolate mofetil [32,33] and tacrolimus [34,35], have been extensively studied, with controversial results.
A number of probe drugs for the in vivo study of MDR1 activity have been suggested but none of them is perfect [36,37]. Because of the low substrate specificity of many drug membrane transporters, many probe drugs may reflect the activity of several transporters. For instance, a typical probe drug for MDR1, fexofenadine, is also a substrate of several OATP influx transporters [37]. In this study, talinolol was chosen as a probe drug for drug membrane transporters. Talinolol appears suitable as a membrane transporter probe drug since less than 1 % of an orally administered dose was recovered as metabolites in urine [38,39]; thus, metabolism plays only a minor role in its elimination.
Evidence for which transporters are possibly relevant in the pharmacokinetics of talinolol is based on multiple data sources. Talinolol is widely considered as an MDR1 probe drug both in vitro and in vivo [36]. Several investigators used talinolol in caco-2 cells as a model substrate of MDR1. Plasma concentrations after oral administration of talinolol were substantially (4.5-fold) higher in a MDR1 knockout rat compared with the wild-type rat [40]. Clinically, net intestinal secretion of talinolol was inhibited by the MDR1 inhibitor verapamil [41] and carbamazepin [42]. Additionally, rifampin-induced MDR1 and MRP2 expression resulted in decreased oral bioavailability of talinolol [43] and corresponding effects were seen with St. John's wort [44]. Unexpectedly, two inhibitors of MDR1, grapefruit juice and verapamil, decreased oral bioavailability of talinolol, which was explained by preferential inhibition of intestinal influx transporters by polytropic inhibitors like verapamil [45,46]. According to these data, it is very likely that MDR1 modulates the pharmacokinetics of talinolol in humans to a relevant extent.
MRP2 may also modulate the pharmacokinetics of talinolol. Expression of both MDR1 and MPR2 is greatly increased by typical inducers like carbamazepin and rifampin and the effects of these inducers on talinolol pharmacokinetics may thus also be explained by an involvement of MRP2. This is also supported by the low talinolol oral bioavailability found in carriers of the MPR2 exon 10 Val417Ile genotype (G1249A) [47].
A comprehensive in vitro screen of all influx and efflux transporters possibly relevant in talinolol pharmacokinetics has not been performed to our knowledge. Preliminary data indicated that talinolol may be a substrate of OATP1B1 [48] and with its cationic structure, talinolol may be a substrate of OCT1. In addition, other efflux transporters, including the polymorphic MDR5 (ABCB5) and BCRP (ABCG2) [49], may modulate the pharmacokinetics of talinolol; therefore, we also explore here the impact of polymorphisms known to be functional in these transporters.
The aim of the present study was to reveal how much of the variation in talinolol pharmacokinetics is due to heritable factors. Secondary questions were whether we can reproduce the effects of genetic polymorphisms which were associated with talinolol pharmacokinetics in earlier publications and how suitable a much lower test dose of talinolol (2.5 mg) might be for in vivo phenotyping. A low dose is apparently more safe and the lower dose was also scientifically interesting because the impact of MDR1 on talinolol pharmacokinetics might depend on the dose [50].

Subjects and study design
Monozygotic (MZ) and same-sex dizygotic (DZ) twin pairs were included if they were healthy according to medical history, clinical examination, electrocardiogram, and standard clinical biochemistry and hematology tests. Except for oral contraceptives no other drugs were allowed for 1 week prior to and 48 h after administration of talinolol.
A single dose of 50 mg talinolol (Cordanum®, AWD.pharma, Dresden, Germany) was administered to 114 subjects. Among these subjects were 43 MZ and 13 DZ twin pairs; two single twins were excluded from the analyses since the second twin could not participate in the study. Additionally, one MZ pair was excluded from the analyses because of missing concentration data for the last blood sample 22 h after talinolol administration. Therefore, all analyses on 50 mg talinolol are based on data from 110 subjects (42 MZ and 13 DZ twin pairs). Per protocol, talinolol 50 mg was administered on three different occasions to each subject with an at least 7-day wash-out period in between. Blood sampling was done prior to and 0.5, 1, 2, 3, 4, 5, 6, and 22 h after talinolol administration. Talinolol was part of a phenotyping drug cocktail in which midazolam, torsemide, metoprolol (all intravenously) [51], and caffeine (orally) [52] were also administered in a sequential order in the first 2 h of each study day. All the substances in this cocktail are not known to have any pharmacokinetic interactions and talinolol was the last administered drug and was given 1 h after caffeine.
In an additional add-on study aiming to compare lowdose talinolol, which is presumed to lack relevant cardiovascular effects, 2.5 mg talinolol was administered to 73 subjects: 29 MZ and 7 DZ twin pairs. One single twin was excluded from the analyses. The capsules containing 2.5 mg of talinolol were prepared from Cordanum® 50 tablets, which were ground and used to refill gelatin capsules in 2.5 mg portions. In this add-on study, blood sampling was done prior to and 0.5, 1, 1.5, 2, 3, 4, 6, and 8 h after talinolol administration.
Blood samples were centrifuged for 10 minutes (4000 rpm, 4°C) and plasma samples were stored at −20°C until laboratory analysis.

Talinolol plasma concentrations
Talinolol plasma concentrations were determined by liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis using deuterium labeled talinolol-d5 (Toronto Research Chemicals, Nr. T005002) as internal standard. For the 50 mg talinolol study sample preparation with protein precipitation and HPLC separation were performed as described [51]. Samples from the lowdose study were worked up with solid phase extraction. LC-MS/MS analysis was carried out on an Agilent 6460 triple quadrupol mass spectrometer (Agilent, Waldbronn, Germany) coupled to an Agilent 1200 HPLC system. Ionization mode was electrospray (ESI), polarity positive. The mass spectrometer was operated in the multiple reaction monitoring (MRM) mode using the transitions m/z 364.3 to 308 and m/z 369.3 to 313 for talinolol and the internal standard, respectively. For the 50-mg dose study, the limit of quantification (LOQ) was 1.5 pmol/ ml. Quality control samples over the whole concentration range could be determined with a coefficient of variation (CV) better than 2.1 %. For the low-dose study, the LOQ was 0.2 pmol/ml. Over the whole concentration range (from 0.2 to 30 pmol/ml), a CV better than 5 % was achieved.

Statistics
Pharmacokinetic parameters were estimated with WinNonlin (Pharsight Corporation, Mountain View, USA). Total clearance, the primary parameter, normalized to bioavailability (Cl/F) was calculated as dose/AUC infinity and in this study is referred to as "clearance". The area under the concentration time curve (AUC) was calculated by the linear/log trapezoidal rule. AUC infinity values were extrapolated based on the last predicted concentration using the terminal elimination rate constant (lambda z). AUC 7h reflects the AUC in the first 7 h after dosage. Maximum concentration (C max ) and time of maximum concentration (t max ) are given as measured. The terminal half-life (t 1/2 ) was calculated as ln(2)/lambda z. The volume of distribution based on the terminal phase (V z ) was calculated as Dose/(lambda z × AUC infinity ).
Heritability was estimated by structural equation modeling using the "mets" package for the statistical programming environment R [53,54]. Variation in clearance was decomposed into additive genetic effects (A), dominant genetic effects (D), common environmental effects (C), and unique environmental effects (E). Fit of the models ACE, ADE, AE, and CE was tested by the Akaikeinformation criterion (AIC). In addition, the repeated administration of 50 mg talinolol to each subject was used to calculate the genetic component (rGC) as described by Kalow et al. [55,56]. Variance within (Vw) the subjects and variance between (Vb) the subjects were calculated for all subjects who received 50 mg talinolol on three different occasions. The mean of 50 calculations of rGC is given. For each calculation of rGC only one randomly selected sibling of each pair was used, since the two siblings of each twin pair are not independent units.
The non-parametric Mann-Whitney U test was used for comparison of two groups and the Jonckheere-Terpstra test for comparison of more than two groups. In the analyses of the effects of genetic polymorphisms on talinolol clearance, an adjustment for multiple testing was done by using the Bonferroni correction method. Due to the high number of tests on genetic polymorphisms (ten in total), significance was determined if p < 0.005. Multiple linear regression analysis was performed for evaluating the effects of the genetic polymorphisms as well as the confounders sex, age, body mass index, consumption of protein, and consumption of vegetables. Protein and vegetable consumption was recorded using validated nutrition questionnaires [57] and calculated as the mean of items "meat", "sausage", "fish", "dairy products", and "eggs" and as the mean of items "salad and raw vegetable" and "cooked vegetable", respectively.

Results
Heritability of the variation in pharmacokinetics of talinolol was studied in 110 volunteers (42 monozygotic (MZ) and 13 dizygotic (DZ) twin pairs). No serious adverse events related to the study medication were reported. No statistically significant differences in the demographic data between MZ and DZ twin pairs were observed (Additional file 1).
Talinolol total clearance (Cl/F) measured after 50 mg talinolol varied 3.8-fold (in DZ) and 8.8-fold (in MZ); after adjustment for body weight, variation in clearance remained high with 2.9-fold and 6.3-fold in DZ and MZ twins, respectively. Similarly, strong variation was observed in AUC infinity and AUC 7h (Table 1). No sequence effects were observed, i.e., the mean pharmacokinetic parameters were not significantly different between the study days. Clearance varied within subjects up to threefold between the three different study days (Fig. 1a)  DZ than in MZ twin pairs (Fig. 1b, c). This indicates that common environmental effects substantially influenced the variation of the clearance. According to structural equation modeling, common environmental (C) and unique environmental effects (E) best explained the variation in the clearance of talinolol ( Table 2). Common environmental effects seem to account for 53.5 % and unique environmental effects for a further 46.5 % of the variation in the clearance (Table 2).
An alternative model (AE) explained 50 % of the variation by additive genetic effects and 50 % by environmental effects. However, statistically this model was clearly inferior according to the AIC.
The pharmacokinetics of drugs usually depends on body weight and body weight is partially also genetically determined. Results were similar after adjustment of talinolol clearance for body weight with slightly more unique environmental effects (C = 45 % (95 % CI 24-66 %), E = 55 % (95 % CI 34-76 %)).
An alternative indicator for heritability can be estimated from the comparison of within-and betweensubject variation. Based on the within-and betweensubject variance with the three times repetition of 50 mg talinolol, the genetic component (rGC) was 0.38 (95 % CI 0.35-0.41) for talinolol total oral clearance and 0.53 (95 % CI 0.50-0.57) for talinolol AUC (Table 3). Withinand between-subject variance was similar for t max and C max , which indicates there were no relevant genetic influences on these two parameters (Table 3).
Although our study indicated only low to moderate heritability in talinolol pharmacokinetic variation, there may be up to 38 % heritability in the clearance according to the repeated measurement approach. Therefore, we evaluated the influence of genetic polymorphisms on the efflux transporters MDR1, MDR5, MRP2, and BCRP as well as the most relevant polymorphisms in the influx transporters OCT1 and OATP1B1 on talinolol clearance. Considering the moderate sample size of our study, only those polymorphisms which have been associated with transport activity in earlier studies were analyzed. Heterozygous or homozygous carriers of MDR1 1236 T alleles and MDR1 2677 T alleles showed a significant increase (p = 0.0025 and 0.0015, respectively) in the total oral clearance of talinolol (Table 4). Clearance was increased by 44 and 48 % in homozygous carriers of MDR1 1236 T and 2677 T alleles compared to homozygous carriers of 1236C or 2677G alleles, respectively. All other polymorphisms in the genes coding for the efflux transporters MDR1, MRP2, MDR5, and BCRP were not significant predictors of talinolol total oral clearance (Table 4). Concerning the influx transporters OATP1B1 and OCT1, after adjustment for multiple testing, none of the variants known to be functional showed any significant association with talinolol clearance (Additional file 2).
Multiple linear regression analysis was performed to evaluate the possible influences of demographic and environmental factors potentially modulating the in vivo activity of drug membrane transporters (Table 5). In this multifactorial analysis none of the genetic polymorphisms remained significant, but sex, body mass index, protein, and vegetable consumption significantly explained variation in the talinolol clearance; these factors each explained only about 4 % of the total oral clearance of talinolol.
In addition to the 50 mg study, a low-dose study using 2.5 mg talinolol was performed. This study included 29 MZ and 7 DZ twin pairs. To enhance the feasibility of phenotyping, we restricted blood sampling to a shorter interval and therefore AUC 7h was the primary parameter. The median of the AUC 7h was 0.58 mg*min/l and varied between 0.36 and 1.42 mg*min/l. Between-twin pairs Pearson's correlation coefficients of the AUC 7h were similar for both the 50-mg and the 2.  . While significant inter-individual variation in the time of maximum blood concentration was observed after administration of 50 mg talinolol (Fig. 2a), variation in the time-concentration curves was apparently much lower in the 2.5 mg group (Fig. 2b). After 50 mg talinolol, the time of maximum plasma concentration (t max ) varied between 1 and 4.1 h whereas after 2.5 mg, t max was 4 h after administration in all 72 subjects (Fig. 2a, b). The maximum plasma concentration (C max ) after 2.5 mg talinolol administration was 3.94 μg/l (median) and varied between 1.67 and 13.2 μg/l. Accordingly, the dose adjusted C max was 1.57 μg/l/mg in the 2.5-mg study phase and 1.85 μg/l/mg in the 50-mg study phase.
The AUC 7h for the 50-mg and the 2.5-mg study phases showed a significant (p = 0.035) but only weak correlation, with a Person's correlation coefficient of 0.25 (95 % CI 0.18-0.45) (Fig. 2c). Thus, according to the coefficient of determination, only about 6 % of the variation observed after administration of either dose was predictive for the variation in the other dose.

Discussion
The impact of genetic variation on the activities of MDR1 and MRP2 has been extensively studied in the past 20 years but is still controversial [10,11]. Conflicting results have been reported, particularly for the abundant and widely studied variants in MDR1 (C1236T, G2677T/ A, and C3435T) as well as for the -C24T and G1249A variants in MRP2 [10]. Also, the genotype-phenotype correlations for many other frequent variants have mostly not been consistently reproduced, whereas those variants with strong penetrance and clear genotype-phenotype correlations are relatively rare. In this situation, we went back in the logical sequence of research to the important first  A/A 0 (-) -Data are given in mean ± standard deviation. a There were significant differences between heterozygous (C/T) and homozygous (T/T) carriers of the MDR1 1236 T allele and homozygous carriers of the 1236C allele (C/C) as tested with the Jonckheere-Terpstra test (p = 0.0025). b There were significant differences between heterozygous (G/T) and homozygous (T/T) carriers of the MDR1 2677 T allele and homozygous carriers of the 2677G allele (G/G) as tested with the Jonckheere-Terpstra test (p = 0.0015). Significance was determined after correction for multiple testing for p < 0.005 (Bonferroni correction) NS not significant. a The correlation is given for the total model with all factors. The r 2 (coefficient of determination) may indicate the fraction of the total variation explained by the respective factors question, namely, how much of the variation in drug membrane transport as tested with in vivo probe drugs is caused by heritable factors? One approach to answer this question and to differentiate between genetic and environmental factors is the use of twin studies. The results of twin studies may provide a unique basis to direct further research [58]. If a major part of the variation in the pharmacokinetics of probe drugs can be explained by genetic factors, then further approaches like whole-genome sequencing to search for the underlying factors may be promising. If results from twin studies reveal no or only moderate genetic effects, then such genome-wide screening might not be very promising or could require major effort to achieve adequate statistical power. We chose talinolol as a probe drug because it is not metabolized to a relevant extent and in vitro and in vivo studies revealed that it may be a good probe drug for MDR1 as well as probably for MRP2 [37]. Generally, a probe drug has great heuristic potential allowing extrapolation from effects in one drug to numerous other drugs. However, this probe drug approach has limitations because in reality pharmacokinetics of every probe drug is not dependent on just one transporter or enzyme but probably on several, and many transporters or enzymes have multiple substrate binding sites with differential substrate affinities. With talinolol, we do not know quantitatively how much of the AUC or total clearance depends on MDR1 since data obtained in the MDR1 knockout rat [40] may be compromised by unspecific or secondary effects of the knockout; also, other factors limit extrapolation from rat to human.
More than usual with pharmacokinetic data, the mean pharmacokinetic parameters of talinolol differed between the studies. Its mean oral clearance was 0.93 l/ min in our study and varied between 0.58 l/min [59] and 1.95 l/min (calculated from dose divided by given AUC infinity ) [45] in other studies. Although this variation may result from minor differences in the pharmaceutical preparations, data analysis, and study populations, it could also indicate that some not yet clearly defined environmental factors have a major influence on the pharmacokinetics of talinolol.
To the best of our knowledge this is the first twin study on the heritability of talinolol pharmacokinetics as a marker of variation in drug membrane transport activities. We observed unexpectedly small heritability. The correlations between the siblings were nominally even higher for DZ than for MZ twin pairs (Fig. 1b, c) and, consistent with this, structural equation modeling revealed that common and unique environmental effects best explained the variation in talinolol oral clearance. Mechanistically, unique environmental effects include everything that acted randomly and not in the same manner in both siblings, whereas common environmental  Fig. 2 a, b Concentration time curves of one study day of the 50 mg talinolol study phase (a) and the 2.5 mg talinolol study phase (b). c Correlation of the AUC 7h after the administration of 50 mg and 2.5 mg talinolol. Shown are all 72 individuals who received both dosages. AUC 7h area under the curve in the first 7 hours after application effects may include everything that is common to the siblings arising during pregnancy, childhood, and later life. Such common environmental effects may include all types of epigenetic effects but also any other factors which may be common due to growing up in the same family and environment.
The twin-study independent approach of Kalow et al. [55,56], which uses repeated drug administration, revealed a low genetic component (rGC) of 0.38 and is generally in good agreement with the result from structural equation modeling. However, this component of 38 % includes both genetic effects and common environmental effects. This means that less (probably even much less) than 38 % of the variation is due to heritable factors. In contrast to the low genetic component in this study, other studies reveal high genetic components for other pharmacological variability, e.g., between 0.95 and 0.98 for the activity of N-acetyltransferase 2 (NAT2) [52,55], 0.96 for plasma clearance of midazolam [60], 0.94 for the ethinylestradiol serum AUC [60], and 0.91 for the plasma AUC of metoprolol [51].
Several genetic polymorphisms in drug membrane transporters have already been analyzed in relation to talinolol pharmacokinetics. In our study, the genetic variants of MDR1 C1236T and G2677T/A were significantly associated with talinolol oral clearance, but this association was weak and even not significant after including other factors in a multifactorial analysis. For both polymorphisms clearance was enhanced in subjects heterozygously or homozygously carrying the 1236 T and 2677 T alleles, indicating higher activity of MDR1 compared to homozygous carriers of the 1236C or 2677G alleles. In line with this, both polymorphisms showed a lower AUC in subjects carrying hetero-or homozygous variants (1236 T and 2677 T or A) in another independent study on the oral bioavailability of talinolol [44]. However, two further studies found no significant effects of C3435T and G2677T/A [45,61] as well as C1236T [45] on the talinolol AUC, indicating only weak functional effects and/or big effects of other not yet fully understood factors.
In this study we did not observe effects of some frequently studied and apparently functional MRP2, MDR5, and ABCG2 polymorphisms on talinolol clearance. The MRP2 finding is in contrast to Haenisch et al. [47], who reported an association of a lower AUC (and a lower oral bioavailability) and the 1249A variant. However, confirmation of earlier genotype-phenotype associations was not the primary aim of the present study and would have required a substantially bigger sample size, particularly for the quantitatively moderate effects.
The effects of genetic variation in efflux transporters on talinolol pharmacokinetics may be complicated by additional influences of genetically polymorphic influx transporters. A study by Bernsdorf et al. reported a significantly decreased talinolol half-life in carriers of the *1b variant in organic anion transporter OATP1B1 [48]. The *1b variant seems to code for a protein with high activity [62] but, in the study by Bernsdorf et al., subjects carrying the low-activity allele *15 of OATP1B1 also showed a decreased half-life. In line with these results, our study revealed that heterozygous carriers of the *1b allele (n = 21) tended to have a higher clearance compared to carriers of the wild-type allele *1a (Additional file 2) but homozygous carriers of the *1b allele (n = 4) had a lower clearance. The lack of consistency and the lack of a consistent effect in our study of the low activity allele *5 do not support a relevant role for OATP1B1 in the pharmacokinetics of talinolol.
Talinolol is a relatively hydrophilic drug and with a pKa of 9.3, about 98 % of the molecules are positively charged at physiological pH [50]. It is therefore a possible substrate of organic cation transporters [44]. For this reason we studied the influence of genetic variants in the genetically highly polymorphic transporter OCT1 on talinolol clearance. Surprisingly, although not significant, talinolol oral clearance tended to be increased in carriers of one or two reduced activity OCT1 alleles. Further in vitro research is required to elucidate whether OATP1B1 or OCT1 may enhance cellular uptake of talinolol.
Interestingly, protein and vegetable consumption both statistically significantly increased talinolol clearance. Our study was not designed to elucidate the underlying substances and mechanisms but it is reasonable that the pharmacokinetics of the mostly not metabolized drug talinolol is strongly dependent on transport activities in the intestinal mucosa and expression in these cells should depend on diet.
In an additional study, a subgroup of the volunteers received a low oral dose of 2.5 mg talinolol. The aim of this low-dose study was to enable a comparison between it and the 50 mg study. The so-called microdosing design has repeatedly been shown to be a valuable tool in the drug development process [63]. Although microdosing is defined by administration of doses below 100 μg, and in this sense we did not perform microdosing, the observations with our low range millidosing are notable. Interestingly, we observed quite different results compared to the therapeutic dose. The dose-normalized AUC 7h was only about 50 % in the low dose talinolol group compared with the AUC from the comparable time interval in the 50 mg talinolol group. Also, t max was achieved significantly earlier in the 50 mg talinolol group. These differences were already noted by Wetterich et al. [50]. One explanation may be that, in the high dose group, efflux transporters like MDR1 may be saturated very early so drug elimination, especially due to intestinal efflux, is delayed [50]. The very low correlation of the AUC 7h for 2.5 mg and 50 mg talinolol (Fig. 2c) may similarly indicate first that this may be one example of a substance for which microdosing is not highly predictive for pharmacokinetics in therapeutic doses and second that the relevant transport processes and proteins involved may be different depending on the doses. This is supported by the fact that this correlation (Fig. 2c) was much lower than the correlation between the different study days with the same dose and between the siblings (Fig. 1d, e). In contrast to our study, another study with another MDR1 probe drug, fexofenadine, showed more rapid absorption of the drug with the smaller dose [64]. In this other study, however, 100 μg of fexofenadine was administered in 10 ml physiological saline and quickly swallowed and the high dose of 120 mg was administered as a tablet. Therefore, the different formulations may explain the contradictory results to our study.

Conclusions
The absorption, distribution, and elimination of talinolol seem to be mainly determined by environmental effects. This may indicate that the in vivo activity of MDR1 may also be dominantly determined by environmental factors. Some data presented in this study, however, may raise doubts about whether or not talinolol is really a good in vivo probe drug for MDR1. Further experimental and clinical research on the role of OATP1B1 and OCT1 may be scientifically interesting, but from our data one might simply conclude that frequent genetic polymorphisms with dominant effects on talinolol pharmacokinetics do not exist.