alexa Know-how and Know-why Nutrients may be Less Bioaccessible and Less Bioavailable due to Proton Pump Inhibitor - Food Interactions and Incompatibilities Involving Metal-Aquo Complexes | Open Access Journals
ISSN: 2161-0509
Journal of Nutritional Disorders & Therapy
Like us on:
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Know-how and Know-why Nutrients may be Less Bioaccessible and Less Bioavailable due to Proton Pump Inhibitor - Food Interactions and Incompatibilities Involving Metal-Aquo Complexes

Helena Jenzer*, Irene Marty, Sandra Büsser, Marta Silva, Franziska Scheidegger-Balmer, Linda Jennifer Ruch, Sofia Martins, Noëmi Dajanah Maurer-Brunner, Francesca Rotunno and Leila Sadeghi

Bern University of Applied Sciences BFH, Health Division, R&D Nutrition and Dietetics, Bern, Switzerland

*Corresponding Author:
Prof. Dr. Helena Jenzer
Bern University of Applied Sciences, Health Division, R&D Nutrition and Dietetics
Murtenstrasse 103008 Bern, Switzerland
Tel: +41 31 848 45 57
E-mail: [email protected]

Received date: May 03, 2016; Accepted date: June 15, 2016; Published date: June 23, 2016

Citation: Jenzer H, Marty I, Büsser S, Silva M, Balmer FS, et al. (2016) Know-how and Know-why Nutrients may be Less Bioaccessible and Less Bioavailable due to Proton Pump Inhibitor - Food Interactions and Incompatibilities Involving Metal-Aquo Complexes. J Nutr Disorders Ther 6:191. doi:10.4172/2161-0509.1000191

Copyright: © 2016 Jenzer H, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Journal of Nutritional Disorders & Therapy

Abstract

Background: Proton pump inhibitors change gastric pH from around 2.0 to 2.5 to more than 4.0 for up to 16 hours per day and suppress gastric function widely. Risk factors assigned to long-term inhibition of gastric acidity arise from cleavage-resistance of peptides and glycosides, mucosal degeneration and leak, loss of bactericidal action, and modification of absorption kinetics of medicines and nutrients. This article aims to contribute to wisely use of proton pump inhibitors and to recommend nutritional options.

Methods: A systematic online literature research was performed on usual platforms. Recommendations rely on a multidisciplinary focus group assessment. Explanations arising from the retrieved references were tested for consistency by titration of iron solution from acidic to basic pH while observing precipitation.

Results and discussion: Literature describes bacterial overgrowth, community and hospital-acquired pneumonia, childhood asthma related to PPI treatments of mothers in pregnancy, sensitization to food allergens in the elderly and in pregnant women (as progesterone slows down gastric emptying), deterioration of intolerances, and various diseases such as celiac and inflammatory diseases. In addition to pathologies, bioavailability of medicines may be modified dramatically. For micronutrients, aquo-complexes of metal ions revealed to be a neglected issue in research of food-drug interactions arising from PPI treatments.

To prevent these complications, a focus group from a clinical support team recommends intermittent and ondemand strategies, alternative antacids, avoidance of high allergenic food, buffering, pepsin replacement, stimulation of digestion and peristalsis, and physical activity, and medicines review and reconciliation.

Conclusion: Proton pump inhibitor safety profiles are troubled by risk factors arising from inappropriate longterm use. Drugs’ bioavailability may increase as a result of mucosal hyperpermeability, or decrease as a result of altered dissociation. Care should be given to substrates with pKa<4.5 as well as to micronutrient supply. At least children and pregnant women should prefer alternative antacids.

Keywords

Bioavailability; Metal-aquo complex; Gastric acidity; Hypochlorhydria; Food-drug interactions; Medicines; Nutrients; Proton pump inhibitors; PPI adverse effects; PPI safety

Introduction

Gastric acid secretion is stimulated by meals, mainly by protein, calcium (both major fractions of milk), and carbohydrates. Pepsin activation and enzymatic protein digestion depend on a pH<3.0 to 3.5. Mean gastric fasting pH is 2.15 for men and 2.8 for women [1]. As a result of its logarithmic scale, this apparently small pH difference corresponds to a nearly 5-fold excess of gastric protons in males. Higher proton release in men seems to be justified by the physiological need to support muscle mass. The use of proton pump inhibitors (PPIs) to treat disorders such as gastroesophageal reflux disease (GERD), bleeding peptic ulcers, or severe reflux disease, changes gastric pH permanently to >4.0 [2]. In pharmacotherapy, to prevent peptic ulcers arising from non-steroidal anti-inflammatory drugs, it is widely accepted to combine them with PPIs. This combination treatment may last over several months or years in the case of arthrosis and degenerative rheumatic diseases.

Peptide bonds of proteins and acetal bonds of carbohydrates are both hydrolyzed enzymatically and non-enzymatically in an acidic environment. A major problem of raising gastric pH permanently is impaired non-enzymatic as well as acid catalyzed cleavage of peptide and glycosidic bonds, i.e. malfunction of proteolysis and hydrolysis of di-, oligo-, and polysaccharides. In the modified gastric environment, drugs and nutritional components may be differently soluble, differently dissociated, and/or differently hydrolyzed, and therefore have modified absorption and bioavailability profiles. The topic is of major public health importance due to high prevalence of gastrointestinal pathologies and number of PPI prescriptions worldwide, estimated to some 120 million annually [3,4].

Multiple factors have an impact on bioavailability of drugs, i.e. [5]

• The drug’s profile related to solubility and dissolution, i.e.

o Dissociation degree

o Hydrogen bond building

o Polar van der Waals surface area

o Molecular weight, size, shape

o Polar functions (hydrophilic – lipophilic balance)

o Molecular flexibility

• The drug’s permeability relying on physiological factors, i.e.

o Preferred absorption site

o Mechanisms of membrane crossing

■ By passive transport according to Fick’s law

■ By active mono- and/or bidirectional (efflux) transporters

• Lipid / bile acid transporters

• Monocarboxylate (organic anion) transporters

• Organic cation transporter

• Nucleoside transporters

• Intestinal dipeptide transporters

• Amino acid transporters

• Vitamin transporters

• Phosphate transporters

• P-glycoprotein transporters

■ Food effects with fat content

■ Surfactants

■ Gastric emptying

■ Transmucosal fluid flow (known as “solvent drag”)

■ Metabolism by CYP450 isoenzymes (mainly CYP3A4,5,7)

pH used to be measured either by potentiometry or by titration in older methods and reflect a value at a specific moment [6-8]. Results are differently integrated by the authors to the percentage of time intragastric pH is below 4. Thus, these studies are of limited comparability. A more recent and refined approach to measure gastric acidity proposes to use an acidity index. This index weighs true molecular amounts of protons rather than pH [9].

The consequences of decreased long-term safety of PPIs and the stop of gastric functioning on nutrition are still understudied and conversely discussed.

The aim of this work is to assess the impact of permanent gastric acidity modification on the bioavailability of nutrients and medicines, and to propose alternative pharmaco-therapeutic and nutritional treatment options.

Materials and Methods

A systematic literature research was performed on Cochrane Library@, Medline®, Google Scholar®, CC Med®, Medpilot®, and DIMDI®. Keywords were PPI, drug-induced hypochlorhydria, digestibility, safety, pregnancy, allergy, in vivo, human, acidity, replacement, and/or nutrient. More specific biochemical mechanisms were researched in a further manually performed ad hoc search. Further data was retrieved from product monographies dedicated for hospital pharmacy medicines information services.

Explanations arising from the references’ interpretation were tested by titration of iron solution from acidic to basic pH conditions while observing precipitate formation. These simple tests were performed to confirm precipitation formation beginning around pH = pKa.

Therapeutic options are relying on a focus group approach integrating an interdisciplinary team of physicians, hospital pharmacists, and nutritionists.

Results and Discussion

Some risk factors of PPI-induced long-term inhibition of gastric acidity are of particular importance for nutritional assessment or nutrition support, i.e. [4]

• Loss of bactericidal effect

o Bacterial overgrowth

• Mucosal degeneration

o Transmucosal leak

o Hyperpermeability

• Modified absorption kinetics

o Reduction or increase of bioavailability of nutrients such as vitamins and oligoelements

o Reduction or increase of bioavailability of medicines

Ad loss of bactericidal effect

Peptic digestion is incomplete in the first two years of life. The antiseptic effect of acidity in the stomach develops within a few hours after birth. In full-term babies, the gastric acidity changes within one hour from 6.1 to 5.4, within 2 hours to 3.1 and within six hours to 2.2. pH increases afterwards for 10 days and decreases again slowly and slightly. Acid output similar to adults is reached by 24 weeks. Full adult values are not reached before an age of approximately 2 years [10]. Preterm born babies have a gastric pH>4 for 80-90% of time, the acidity rising slowly with age [11].

As bactericidal effect decreases with raising pH, the risk for bacterial, viral, and prion-associated infections increases. An increase in gastric pH to around 4.0 is observed for infants aged 1 to 12 months with chronic diarrhea and protein malnutrition, combined with bacterial overgrowth, which contains essentially Gram-negative bacilli in 57% of the cases. This bacterial overgrowth happens at the moment of the evolution of the disease to a chronic state. Breast-fed babies do not have bacterial overgrowth of gram-negative bacilli and no diarrhea, although they have a similar gastric pH to bottle-fed babies. This may be related to the transfer of protective factors e.g. immunoglobulines from lactating mothers. Therefore, an adequate gastric pH is determinant for complication-free adaption, mainly if babies are not breast-fed [12].

Children of 4 to 36 months suffering from GERD and treated with H2 antagonists or PPIs for 8 weeks showed a higher risk for acute gastroenteritis and community and/or hospital acquired pneumonia, although otherwise healthy. These risks sustain on stopping the therapy [13]. Alteration of gastric acid secretion may also bring with it chronic Helicobacter pylori infections. As acidity is also reduced in the upper aerodigestive tract, pneumonia is arising from increased bacterial larynx and esophagus colonization. In addition, Clostridium difficile – associated diarrhea is a complication of PPI treatment in adults and in children increasing in combination with statins. On behalf of microbiology, an acidic gastric pH of <3 is determinant for bactericidal activity and thus protection against bacterial overgrowth of Clostridium difficile, Capylobacter jejuni, and Salmonella ssp [13]. This is also true for the inflammation, ulcer, and stomach cancer associated Helicobacter pylori which produces big amount of urease leading to a shift in gastric pH from between 2.2-2.8 to a range of 6-7 [14].

Ad mucosal degeneration

Alterations of gastric pH increases the risk for polyps, enterochromaffin-like (ECL) cell hyperplasia, carcinoid, gastrinoma, and cancer, in combination with transmucosal leak and hyperpermeability proximal to duodenum, occurring within a few days after PPI therapy start and being reversible within a few days of discontinuation. Undigested persisting proteins, peptides, allergenes and drugs may be absorbed more readily. Digestion-resistance and persistence of food protein during gastric transit are documented risk factors for sensitization to food allergens for elderly patients around 65 years or pregnant women, who suffer also from slower gastric emptying due to progesterone. Concomitant PPI use and degradation of various pathologies such as lactose intolerance, celiac disease, atrophic gastritis, rheumatoid arthritis, and/or diabetes mellitus, are reported being correlated positively. Some are gender-different as well as a result of estradiol-receptor-dependent mast-cell activation [15-19]. Community and hospital-acquired pneumonia show an increased risk ratio of 1.89 in PPI patients. An increase of asthma among children is also associated with PPI treatments of their mothers in pregnancy. The association is evident as a result of increasing food-specific IgE antibodies within 3 months and is postulated to arise from increased type 2 helper cell bias in the offspring, thus from predisposition to increased atrophy [20].

Ad modified absorption kinetics

In addition to allergens, higher and potentially dangerous amounts of drugs may be available in the course of long-term PPI treatment as a result of drug-drug and food-drug interactions. On the other hand, a decreased bioavailability due to long-term PPI pharmacotherapy is described for vitamins’ and for oligoelements’ absorption, e.g. of ascorbic acid (pKa 4.19), cyanocobalamin, zinc, iron, magnesium, folate, and calcium depending on their salt and thus pH-dependent solubility [21-25]. Calcium depletion is likely to induce osteoporosis, while the risk of hypomagnesemia due to long-term PPI treatment has been subject of an FDA notification to healthcare professionals and the public in March 2011 [26]. Some of these deficiencies are reported to be not significant while short-term treatments. However, such studies include in general very few patients.

Modification of absorption kinetics is described for many drugs such as ketoconazole, itraconazole, atazanvir, cefpodoxime, cinnarizine, enoxacin, or dipyridamole, which are less bioavailable as a result of altered dissociation, and of nifedipine, digoxin, penicillins, erythromycin, or alendronate, which are more bioavailable as a result of mucosal hyperpermeability [27]. The reason for altered absorption kinetics of medicines can be explained by the change of both solubility and charge. As a result of gradually increasing pH in the gastrointestinal tube and depending on their acid dissociation constant pKa, drugs and nutritional components are differently soluble and differently available for absorption in various parts of the tube. Uncharged solubilized molecules will be readily absorbed by passive diffusion. At pKa = pH, 50% of a molecule is dissociated and 50% undissociated. In a dissociated and charged form, a molecule is worse passively absorbed in the GI tube. Thus, all weak acids bases with pKa<4 can give rise to undesirable effects, if gastric pH will no longer remain in a physiological range but rather be over 4. In this milieu, the fraction of the readily absorbable undissociated amount decreases and the deprotonated form will markedly increase. Generally speaking, weak acids retain a lower fraction of their undissociated state if pH raises and are therefore less bioavailable as a result of lower passive diffusion. Functional groups with an acid dissociation constant pKa<4 such as carboxylic acids, vinylogous carboxylic acids, acid halides, -I-mono- or disubstituted phenols, or sulfonic acids are those who can lead to a loss of bioavailable medicine under PPI treatment, e.g. many non-steroidal anti-inflammatory drugs and ascorbic acid. On the other hand, weak bases will have a higher fraction of undissociated state if pH raises and are therefore more bioavailable as a result of higher diffusion (Table 1 and Figure 1).

Classes / Drug Generic Name (pKa) Structure
Central Nervous System Antipyretics, Analgesics
     • Acetaminophen/Paracetamole (9.38[phenol]/2.2[amide])
     • Phenacetin (2.2)
Benzodiazepines
     • Bromazepam (2.9[4-N]/11.0[1-N])
     • Chlodiazepoxide (4.8[1-N])
     • Clonazepam (1.5[4-N]/10.5[1-N])
     • Diazepam (3.4[4-N])
     • Flunitrazepam (1.8[4-N])
     • Flurazepam (1.9[4-N]/8.2[1-N])
     • Lorazepam (1.3[4-N]/11.5[1-N])
     • Nitrazepam (2.94[4-N]/11.0[1-N])
     • Oxazepam (1.7[4-N]/11.6[1-N])
Skeletal muscle relaxants, anticonvulsants, GABA agonists
     • Valproic Acid (4.8)
     • Baclofen (3.9[hydroxyl]/9.8[amine])
image
Cardiovascular System Anti-arrhytmic agents
     • Quinidine (4.2[quinoline-N]/8.3[quinuclidine-N])
Various anti-hypertensives
     • Captopril (3.7/9.8)
     • Minoxidil (4.61)
     • Timolol (3.9)
     • Nifedipine (3.93)
image
Lung Mucolytic and anti-asthmatic agents
     • Bromhexine (4.0)
     • Cromoglicate (1.1)
image
GI System Gastrointestinal agents
     • Bisacodyl (4.47[pyridine-N])
     • Sulfasalazin (0.6[amine]/2.4[carboxyl]/9.7[sulfonamide]/11.8[phenol])
image
Kidney Diuretics
     • Ethacrynic acid (3.5)
     • Furosemid (3.9/4.7)
     • Torasemid (4.0)
image
Blood COX-1 selective and platelet aggregation inhibitors
     • Acetylsalicylic acid (3.49)
Antifibrinolytics
     • Aminocaproic Acid (4.43)
     • Tranexamic acid (4.3/10.2)
Anticoagulants – Coumarines and Indandiones
     • Acenocoumarol (4.7)
     • Phenprocoumone (4.2)
image
Metabolism Photosensitizing agent and intraoperative tumour identifyer
     • d-Aminolaevulinic acid (4.6)
Vitamins and derivatives
     • Vitamin C (4.17/11.6)
     • Folic acid (4.17)
     • Isotretinoin  (4.0)
COX-2 selective inhibitors
     • Etoricoxib (4.5)
Low-selective COX-2 inhibitors - Oxicams
     • Meloxicam (4.08)
     • Piroxicam (1.86/5.46)
Non-selective COX inhibitors - Anthranilic acid derivatives
     • Flufenamic acid (3.9)
     • Mephenamic acid (4.2)
Non-selective COX inhibitors – Phenyl- and heteroarylacetic acid derivatives
     • Diclofenac (4.15)
     • Etodolac (4.65)
     • Indomethacin (4.5)
     • Ketorolac (3.5)
     • Sulindac (4.7)
Non-selective COX inhibitors – Propionic and arylpropionic acid derivatives
     • Fenoprofen (4.5)
     • Ibuprofen (4.91)
     • Ketoprofen (4.45)
     • Naproxen (4.15)
Non-selective COX inhibitors – Pyrazolones
     • Metamizol-Na (Dipyrone) (2.0)
Histamine H1 receptor antagonists
     • Hydroxyzine (1.8/2.1/7.1)
Antimetabolites
     • Methotrexate (3.8/4.7/5.5)
     • Flucytosine (3.26[amine]/10.7[amide])
Tubulin modulator
     • Colchicine (1.85)
Uricosuric agents
     • Probenecid (3.4)
     • Sulfinpyrazon (3.25)
Biphosphonates
     • Alendronate (2.72)
     • Ibandronate (1.42)
     • Pamidronate (1.43)
     • Risedronate (1.44)
     • Zoledronate (1.42)
image
image
 Anti-infective Agents Sulfonamides
     • Sulfamerazine (2.3/7.1)
Penicillins
     • Penicillin V (2.79)
     • Amoxicillin (2.4/7.4/9.6)
     • Ampicillin (2.7/7.3)
     • Cloxacillin (2.7)
     • Dicloxacillin (2.8)
     • Flucloxacillin (2.7)
     • Methicillin (2.8)
     • Oxacillin (2.8)
     • Propicillin (2.7)
Cephalosporins
     • Cefalexin (4.5)
     • Cefazolin (2.3)
     • Cefixim (3.26)
Tetracyclines
     • Tetracycline (3.3)
     • Chlortetracycline (3.3/7.4)
     • Doxycycline (3.4/7.7/9.3)
     • Minocycline (2.8/5.0/7.8/9.5)
     • Oxytetracycline (3.3/7.3/9.1)
Antituberculosis agents / Antifungal agents / Antiprotozoal agents / Leprostatic agents
     • p-Aminosalicylic Acid (1.7[amine]/2.05/3.9)
     • Salicyclic acid (2.97/13.4)
     • Quinine (4.2[quinoline-N]/8.8[quinuclidine-N])
     • Dapsone (1.3/2.41)
     • Isoniazid (2.0/3.9/10.8[pyridine]/11.2[hydrazide])
     • Rifampicin (1.7[C-8 phenol]/7.9[piperazine-N])
     • Ketoconazole (2.94/6.51)
     • Itraconazole (3.7)
     • Posaconazole (3.6/4.6)
     • Voriconazole (1.76)
Quinolones
     • Enoxacin (6.31)
     • Nalidixic acid (1.0/6.0)
Nitroimidazoles
     • Metronidazole (2.6)
     • Ornidazole (2.6)
Antiviral agents / Nucleoside reverse transcriptase inhibitors
     • Emtricitabine (2.65)
   image
Antidotes Antidote to folic acid antagonists
     • Leucovorin / Ca folinate (3.1/4.8)
image

Table 1: Examples of weak acids and bases prone to a drop of bioavailability in the course of long-term PPI treatment (ascorbic acid, ketoconazole, itraconazole, atazanavir, cefpodoxime, cinnarizine, enoxacin, dipyridamole, …). The solubility of weak acids are particularly concerned by altered pH conditions in the gastrointestinal tube. Missing acidity leads to deprotonation and decreased absorption of the charged molecules.

nutritional-disorders-therapy-Log-conc-diagram

Figure 1: log-conc-diagram.

For oligoelements, apart from dietary factors, another reason for malabsorption must be found [28]. At first sight, their charge does not seem to depend on pH. However, both acidic pH and ascorbic acid (in fruit juice) stabilize iron in its ferrous state by ascorbate chelation. Rapid re-oxidation occurs at neutral pH. Fe(+III) has a high charge density, a small ionic radius (0.067 nm) and easily excited outer electrons, thus prefers oxygen ligands, e.g. phenolate, carboxylate, whereas Fe(+II) has a lower charge density, a larger ionic radius (0.083 nm) and less easily excited outer electrons, thus prefers nitrogen and sulfur ligands, e.g. imidazole, pyrrole, thiolate, or methionine. Metal salts dissolved in water are hydrolyzed. Oligoelement cations exist as aquo-complexes and are therefore weak acids. Polarization of the coordinated water molecules depends on the oxidation state and the size of the cation. Ferric aquo-complexes are more acidic than the ferrous. Deprotonation of coordinated water from ferric aquocomplexes occurs immediately at pH going towards basic, whereas ferrous aquo-complexes remains longer undissociated due to the absence of oxygen and other oxidizing agents. Iron will exist at acidic conditions in the stomach as hexaaquairon(III) ion, [Fe(H2O)6]3+. As pH raises, this aquo-complex is deprotonated to [Fe(H2O)5(OH)]2+ as a result of pKa = 2.2, to [Fe(H2O)4(OH)2]+ as a result of pKa = 3.5, and to [Fe(H2O)3(OH)3]0 as a result of pKa = 6.0. Thus, already at weakly acidic pH and increasingly above approximately pH 5, significant amounts of secondary colloidal iron (III) hydroxides and an amorphous redbrown ferric hydroxide precipitate are formed. After elimination of water from the aquohydroxo complexes, ferric iron will condensate by formation of hydroxo bridges. These mechanisms occurring at natural pH make ferric iron more and more insoluble and unsuitable for absorption.

[Fe(H2O)6]3+ in its deprotonated form is reduced in the distal duodenum to [Fe(H2O)6]2+ at pH between 5 and 6 at the duodenojejunal junction. A first pKa of the ferrous iron aquo-complex is situated at 6.74 and a second at 9.5. Ferrous condensates form only above pH 6 [29-31]. It is well known that iron is mainly actively absorbed as ferrous iron Fe(II+) in the upper duodenal part of the GI tube where the luminal pH gradient raises steeply in the proximal 10 cm of the duodenum. Acidity passes at this site from pH 2 to pH 5 in the fasting state and from pH 1.7 to pH 4.3 in the second and third postprandial hour [32]. Iron absorption is known to be enhanced almost 3fold by ascorbic acid or orange juice. The juice’s acidity is able to override the lack of the diminished acidity produced by the proton pump. On the other hand, the absorption is competed by binding to tannins and components of many beverages derived from tea or coffee. As a result, ferric iron tends to be lost on current PPI treatment and loss of acidity, mainly due to formation of iron (III) hydroxides as colloids or precipitates, therefor lost for reduction to the ferrous state and absorption.

Similar contemplations are applicable for copper, cobalt, zinc, manganese and further elements with important co-factor functions in metabolism. Transportation across the membrane can be further antagonised competitively by other metal ions such as manganese, cobalt, nickel, chrom, or zinc which use the same symporters. pKa values for copper (II+) hexaquo-complexes are 6.8 and 8.5, for cobalt (II+) hexaquo-complexes 8.8 and 12.4, manganese (II+) hexaquocomplexes 10.7 and 12.0, and for zinc hexaquo-complexes 8.96 and 10.1 [33,34].

Discussion of coping strategies for prevention and intervention

Proton pump inhibitors are beneficial for many patients as well as a risk factor for others. Their prescription and use must be carefully assessed. A risk-benefit ratio must be evaluated on a personalized nutrition and medicine basis.

• Alternative antacids, step-down, intermittent and ondemand strategies

o MgCO3 and H2-antagonists have a shorter onset and time of pH>3-4 than pantoprazole 40 mg (median pH = 3.7, pH>4 for 10.8 h) or esomeprazole 40 mg (median pH = 4.7, pH>4 for 16.1 h).

• To avoid high allergenic food

o i.e. Crustacean, eggs, fish, milk, peanuts, soybeans, tree nuts or fruits, and wheat

• Buffering, pepsin replacement, stimulation of digestion and peristalsis

o Carbonated beverages, quinine water, aperitifs, appetizers, and bitter substances (amara)

o Prokinetic agents (domperidone, bromopride, metoclopramide, quinine, erythromycin)

o Mucosal protectors (curcumin, quercetin, alginates, pectins, glycyrrhizin)

o Melatonin (regulates digestion and has structural similarity to omeprazole)

o Pepsin in HCl preparations

• Nutrition and dietary approach combined with physical activity

o High-dietary fiber

o Low-fat diet

o Low-carb diet, i.e. <20 g/d

• Reassessment of pharmacotherapy

o Weak acids (pKa<4.5) lose their undissociated state required for diffusion across membranes.

o Absorption is impaired by membrane-bound CYP3A4,5,7 and efflux transporter P-gp.

Use of antacids (alternatives, step-down, intermittent and ondemand strategies)

Carbonates available over the counter, e.g. in a dose of 1360 mg as calcium-magnesium-salt, will have an onset of about 6 minutes and a time with pH values over 3.0 of about 2½ hours. For an H2-antagonist, e.g. ranitidine 75 mg, the onset is 65 minutes and the time of pH>3.0 is 13 hours and 36 minutes [35]. For pantoprazole 40 mg and esomeprazole 40 mg, the most widely used PPIs, the median 24 h pH are 3.7 versus 4.7 respectively after 5 days of treatment and the times of pH>4 are 16.1 hours (esomeprazol) and 10.8 hours (pantoprazol) respectively. The values have been measured after oral administration to volunteers of Western European countries and New Zealand. Acid production by the proton pump can only be restored through biosynthesis of the H+K+-exchanging ATPase. The production half-life is approximately 50 hours. On PPI stop, a strong rebound hypersecretion is reported, increasing secretory capacity compared to the one existing before the introduction of PPI [2,36-39]. It may be wise to restrictively prescribe antacids which shift pH to >3-4 permanently, mainly in the treatment of pregnant women and children.

Beware of high allergenic food groups

Under PPI treatment special attention has to be paid to the eight food groups which account for 90% of food-allergic reactions, i.e. crustacean, eggs, fish, milk, peanuts, soybeans, tree nuts or fruits, and wheat.

Buffering and substituting gastric juice, stimulation of peristalsis, alternative GERD therapies

After a complete nutrient drink, gastric pH and buffer capacity increase from between 7 and 18 mmol L-1 ΔpH-1 to between 14 and 28 mmol L-1 ΔpH-1. Gastric pepsin levels are doubled. Duodenal values are initially pre- and post-prandial similar, but duodenal pH decreases slowly to 5.2, and buffer capacity increases from between 5.6 mmol L-1 ΔpH-1 to between 18 and 30 mmol L-1 ΔpH-1. Bile salt levels are two to four times higher postprandial. In case of hypoacidity, it may be wise to precondition gastrointestinal pH preprandial by carbonated beverages or a buffering aperitif and/or appetizers. However, protein, carbohydrates, and calcium should be restricted due to their intense stimulation of gastric acidity and secretion. Supply of strong acidic drinks are not recommended due to high sensitivity of patients to acids. Peristalsis may be stimulated by drugs, e.g. domperidone, bromopride, metoclopramide, quinine, or erythromycin (beware of adverse drug reactions), or by bitter substances and amara which are in general terpenoids extracted from officinal plant preparations, e.g. Absinthii herba, aurantii immaturi pericarpium, Cardui benedicti herba, Centaures herba, Citri rec. pericarpium, Condurango cortex, Gentiana radix, Lichen islandicus, Quassiae lignum. These plants may be even more promising in combination with flavonoids due to antiinflammatory and anti-ulcer effects.

Due to its analogy to a partial structure of omeprazole, melatonin, orally given or induced by light exposure, is reported to an alternative to PPI treatment, providing control of the lower esophageal sphincter and neutralization of gastric acid secretion by induction of bicarbonate secretion in the duodenal epithelium. Curcumin and Quercetin have not been explored in human GERD trials, but in vitro and animal data suggest more potential than older medications with alginates, pectins, and glycyrrhizin analogs.

Nutrition and dietary approach

High-dietary fat is increasing GERD risk, while high-dietary fiber is decreasing GERD risk. It is unclear if high-dietary fat effects are independent of obesity. Low-carb diet, i.e. <20 g/d, in obese individuals with GERD significantly reduces acid exposure. Carbonated beverages may be a treatment option on an individual basis, alone or combined with modifying lifestyle and increasing physical activity.

To provide sufficient amounts of micronutrients, combination with ascorbic acid and, as far as supported, acidic beverages is likely to facilitate absorption [40].

Replacement of pepsin

If pepsin secretion is too low, classical pepsin / hydrochloric acid preparations can deliver 2 to 20 mmol protons per single dose.

Reassessment of pharmacotherapy

Absorption upon oral intake is only possible if a substrate can migrate across double-layered membranes by either active carrier driven transport, ion pair or particulate absorption, facilitated or passive diffusion, or hydrophilic diffusion within pores filled with water. Most drugs pass membranes by diffusion. Only undissociated fractions are lipid soluble and can pass membranes by diffusion (Figure 2). Very polar drugs such as poly-alcohols are as a rule hardly bioavailable upon oral intake and may have a laxative effect instead. This is not the case for (primary) nutrients. Monosaccharides, aminoacids, as well as other physiological ingredients of a living cell, or closely related derivatives however, although highly polar as well, are absorbed due to carriers. These membrane passages, above all diffusions, are obviously qualitatively and quantitatively altered with modified acidic-alkaline condition. This situation is even complicated by membrane-bound enzymes such as CYP3A4,5,7 and the efflux transporter P-glycoprotein.

nutritional-disorders-therapy-Structure-comparison-melatonin

Figure 2: Structure comparison melatonin – omeprazole.

Extraction of substrates from the gastrointestinal tract into circulation is comparable to toxicological-pharmaceutical analytics techniques for extraction of undissociated analytes from a solution using the Stas-Otto separation-procedure [41]. The dissociation degree of a substance can be modified by changing pH conditions of the solution. At a pH corresponding to the pKa, 50% of a component is dissociated and 50% not. At a pH of + 1 or – 1 of the pKa value, the ratio is 90% to 10%, at pH of + or -2 this ratio is 99% to 1%. This principle demands that the pH of the aqueous analyte is gradually varied from 1 to 4-5 to 11-12 and to 9-10. On each extraction step, depending on the substances’ pKa, not-dissociated molecules can be extracted using organic solvents. At the end, only very polar, e.g. charged, substances remain in the aqueous fraction.

As a result of gradually increasing pH in the gastrointestinal tube and depending on their acid dissociation constant pKa, drugs and nutritional components are differently soluble and available for absorption in the corresponding part of the tube. Weak acids and weak bases are concerned as long as most of their undissociated form exists at pH ≤ 4. These molecules contain functional groups such as carboxylic acids, acid halides, phenols mono- or disubstituted by -I-groups, sulfonic acids. Weak acids will have a lower fraction of their undissociated state if pH raises and are therefore less bioavailable as a result of lower diffusion, whereas weak bases will have a higher fraction of undissociated state if pH raises and are therefore more bioavailable as a result of higher diffusion (Table 1 and Figure 1). The functional lack of the gastric absorption possibility at pH<4 may be partly compensated in lower parts of the tube at pH>4, if and where the substrate regains its undissociated absorbable form.

Conclusion

In spite of a good short-term safety profile and of the relief PPIs provide to affected patients, it is unanimously accepted that long-term PPI treatment and permanent acidic secretion inhibition brings along some risk factors, e.g. bacterial overgrowth, mucosal degeneration, hyper permeability, altered bioavailability as a result of modified absorption kinetics. Drugs may be more bioavailable as a result of mucosal hyper permeability, or less bioavailable as a result of the missing acid part of the gastrointestinal tube and therefore altered dissociation. Care should be given to substrates with pKa of about pH<4.5. Micronutrients having a function as co-factors in metabolism may be partially lost as dissociation of their aquo-complexes change depending on pH conditions. Whereas the loss of oligoelements such as iron on current PPI treatment may become critic, the loss of NSAID has less consequences as these medicines are given at higher doses eventually still sufficiently above the minimal therapeutic threshold.

Inappropriate long-term PPI therapies should be avoided or replaced in some at risk cases by antacids with a shorter effect. Therapeutic options include alternative antacids, avoiding high allergenic food groups, buffering, stimulation of peristalsis, replacement of pepsin, and reassessment of drug therapy.

Acknowledgement

This work was supported by BFH grant J.003039-42-ERBQ.

References

Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Relevant Topics

Recommended Conferences

Article Usage

  • Total views: 8381
  • [From(publication date):
    June-2016 - Aug 17, 2017]
  • Breakdown by view type
  • HTML page views : 8296
  • PDF downloads :85
 

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

 
© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version
adwords