Component
Sodium
Nutrient element sodium; dietary sodium restriction is distinct from distal luminal sodium delivery or serum sodium concentration.
10 recorded relationships. Experimental role, claim status and evidence remain attached to each record.
How nutrients influence it
Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.
Other things that act on it
Enzymes, hormones, genes, and other components with a recorded effect. These are not nutrients, so they do not count toward the arrows above. Each finding names the chapter that recorded it.
How nutrients reach it in more than one step
Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.
Tracing routes…
What it does
Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.
What it acts on
Low-sodium DASH versus high-sodium control produced mean systolic differences of 7.1 mmHg without hypertension and 11.5 mmHg with hypertension.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/sodium-research/11136953.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7664fc223f123220dd64755a1e9bc4ee3e9942e09b5de444bd789f210f449133", "start_char": 0, "end_char": 1987, "text_sha256": "7664fc223f123220dd64755a1e9bc4ee3e9942e09b5de444bd789f210f449133"}
- experimental_model
- Randomized controlled feeding trial in 412 participants
- exposure
- Three sodium levels for 30 days each within assigned DASH or control diet
- limitations
- Blood-pressure trial, not a hard-outcome trial; DASH changes multiple nutrients and foods. Its combined effect cannot be assigned to one mineral.
- nutrient_topic
- Sodium research collection; topical membership is not evidence of a direct dietary effect. · Sodium
- organism
- Human adults with and without hypertension
- plain_language
- Diet composition and sodium reduction had a combined effect.
- primary_references
- [sodium-p11136953] Effects on blood pressure of reduced dietary sodium and the Dietary Approaches to Stop Hypertension (DASH) diet. DASH-Sodium Collaborative Research Group. (2001). https://pubmed.ncbi.nlm.nih.gov/11136953/ DOI: 10.1056/nejm200101043440101
- tissue_or_cell_type
- Systemic blood pressure
Sodium: gradients, nutrient transport, fluid regulation and loss states (2026-09-17) · lines 1084–1095
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized controlled feeding trial in 412 participants · source_derived_draft · unverified_draft
### sodium-dash-combination Low-sodium DASH versus high-sodium control produced mean systolic differences of 7.1 mmHg without hypertension and 11.5 mmHg with hypertension. Condition category: normal nutrient_topic: Sodium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Diet composition and sodium reduction had a combined effect. organism: Human adults with and without hypertension tissue_or_cell_type: Systemic blood pressure experimental_model: Randomized controlled feeding trial in 412 participants limitations: Blood-pressure trial, not a hard-outcome trial; DASH changes multiple nutrients and foods. Its combined effect cannot be assigned to one mineral. exposure: Three sodium levels for 30 days each within assigned DASH or control diet evidence_span: {"source_cache": "artifacts/sodium-research/11136953.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7664fc223f123220dd64755a1e9bc4ee3e9942e09b5de444bd789f210f449133", "start_char": 0, "end_char": 1987, "text_sha256": "7664fc223f123220dd64755a1e9bc4ee3e9942e09b5de444bd789f210f449133"} [sodium-p11136953] Effects on blood pressure of reduced dietary sodium and the Dietary Approaches to Stop Hypertension (DASH) diet. DASH-Sodium Collaborative Research Group. (2001). https://pubmed.ncbi.nlm.nih.gov/11136953/ DOI: 10.1056/nejm200101043440101
Complete structured claim and evidenceHigh-to-intermediate sodium reduction lowered systolic pressure by 2.1 mmHg on the control diet and 1.3 mmHg on DASH; intermediate-to-low reduction lowered it by another 4.6 and 1.7 mmHg respectively.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/sodium-research/11136953.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7664fc223f123220dd64755a1e9bc4ee3e9942e09b5de444bd789f210f449133", "start_char": 0, "end_char": 1987, "text_sha256": "7664fc223f123220dd64755a1e9bc4ee3e9942e09b5de444bd789f210f449133"}
- experimental_model
- Randomized controlled feeding trial in 412 participants
- exposure
- Three sodium levels for 30 days each within assigned DASH or control diet
- limitations
- Blood-pressure trial, not a hard-outcome trial; DASH changes multiple nutrients and foods. Its combined effect cannot be assigned to one mineral.
- nutrient_topic
- Sodium research collection; topical membership is not evidence of a direct dietary effect. · Sodium
- organism
- Human adults with and without hypertension
- plain_language
- Reducing sodium lowered blood pressure under both tested dietary patterns.
- primary_references
- [sodium-p11136953] Effects on blood pressure of reduced dietary sodium and the Dietary Approaches to Stop Hypertension (DASH) diet. DASH-Sodium Collaborative Research Group. (2001). https://pubmed.ncbi.nlm.nih.gov/11136953/ DOI: 10.1056/nejm200101043440101
- tissue_or_cell_type
- Systemic blood pressure
Sodium: gradients, nutrient transport, fluid regulation and loss states (2026-09-17) · lines 1071–1082
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized controlled feeding trial in 412 participants · source_derived_draft · unverified_draft
### sodium-dash-sodium High-to-intermediate sodium reduction lowered systolic pressure by 2.1 mmHg on the control diet and 1.3 mmHg on DASH; intermediate-to-low reduction lowered it by another 4.6 and 1.7 mmHg respectively. Condition category: normal nutrient_topic: Sodium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Reducing sodium lowered blood pressure under both tested dietary patterns. organism: Human adults with and without hypertension tissue_or_cell_type: Systemic blood pressure experimental_model: Randomized controlled feeding trial in 412 participants limitations: Blood-pressure trial, not a hard-outcome trial; DASH changes multiple nutrients and foods. Its combined effect cannot be assigned to one mineral. exposure: Three sodium levels for 30 days each within assigned DASH or control diet evidence_span: {"source_cache": "artifacts/sodium-research/11136953.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7664fc223f123220dd64755a1e9bc4ee3e9942e09b5de444bd789f210f449133", "start_char": 0, "end_char": 1987, "text_sha256": "7664fc223f123220dd64755a1e9bc4ee3e9942e09b5de444bd789f210f449133"} [sodium-p11136953] Effects on blood pressure of reduced dietary sodium and the Dietary Approaches to Stop Hypertension (DASH) diet. DASH-Sodium Collaborative Research Group. (2001). https://pubmed.ncbi.nlm.nih.gov/11136953/ DOI: 10.1056/nejm200101043440101
Complete structured claim and evidenceLength and head-circumference growth did not differ significantly between treatment groups.
Experimental context and source evidence
- availability_state
- nutrient_deficiency Imported condition classification; unverified.
- evidence_span
- {"source_cache": "artifacts/sodium-research/25406227.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339", "start_char": 0, "end_char": 1645, "text_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339"}
- experimental_model
- Randomized masked trial in 53 infants born before 32 weeks
- exposure
- 4 mEq/kg/day supplemental sodium versus placebo, days 7–35
- limitations
- Study regimen, not a dosing recommendation. Small neonatal trial; improved weight gain is not proof that every blood sodium measurement diagnoses total-body depletion.
- nutrient_topic
- Sodium research collection; topical membership is not evidence of a direct dietary effect. · Sodium
- organism
- Human preterm infants
- plain_language
- The observed growth benefit was not uniform across every growth measurement.
- primary_references
- [sodium-p25406227] Impact of Early Sodium Supplementation on Hyponatremia and Growth in Premature Infants: A Randomized Controlled Trial. (2016). https://pubmed.ncbi.nlm.nih.gov/25406227/ DOI: 10.1177/0148607114558303
- tissue_or_cell_type
- Whole-body growth and serum sodium
- trigger_kind
- nutrient_deficiency Imported condition classification; unverified.
Sodium: gradients, nutrient transport, fluid regulation and loss states (2026-09-17) · lines 993–1004
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized masked trial in 53 infants born before 32 weeks · source_derived_draft · unverified_draft
### sodium-preterm-limits Length and head-circumference growth did not differ significantly between treatment groups. Condition category: nutrient_deficiency nutrient_topic: Sodium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The observed growth benefit was not uniform across every growth measurement. organism: Human preterm infants tissue_or_cell_type: Whole-body growth and serum sodium experimental_model: Randomized masked trial in 53 infants born before 32 weeks limitations: Study regimen, not a dosing recommendation. Small neonatal trial; improved weight gain is not proof that every blood sodium measurement diagnoses total-body depletion. exposure: 4 mEq/kg/day supplemental sodium versus placebo, days 7–35 evidence_span: {"source_cache": "artifacts/sodium-research/25406227.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339", "start_char": 0, "end_char": 1645, "text_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339"} [sodium-p25406227] Impact of Early Sodium Supplementation on Hyponatremia and Growth in Premature Infants: A Randomized Controlled Trial. (2016). https://pubmed.ncbi.nlm.nih.gov/25406227/ DOI: 10.1177/0148607114558303
Complete structured claim and evidenceSupplemented preterm infants had fewer recorded serum sodium values below 135 mmol/L.
Experimental context and source evidence
- availability_state
- nutrient_deficiency Imported condition classification; unverified.
- evidence_span
- {"source_cache": "artifacts/sodium-research/25406227.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339", "start_char": 0, "end_char": 1645, "text_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339"}
- experimental_model
- Randomized masked trial in 53 infants born before 32 weeks
- exposure
- 4 mEq/kg/day supplemental sodium versus placebo, days 7–35
- limitations
- Study regimen, not a dosing recommendation. Small neonatal trial; improved weight gain is not proof that every blood sodium measurement diagnoses total-body depletion.
- nutrient_topic
- Sodium research collection; topical membership is not evidence of a direct dietary effect. · Sodium
- organism
- Human preterm infants
- plain_language
- Very premature infants can need a different sodium provision than older children or adults.
- primary_references
- [sodium-p25406227] Impact of Early Sodium Supplementation on Hyponatremia and Growth in Premature Infants: A Randomized Controlled Trial. (2016). https://pubmed.ncbi.nlm.nih.gov/25406227/ DOI: 10.1177/0148607114558303
- tissue_or_cell_type
- Whole-body growth and serum sodium
- trigger_kind
- nutrient_deficiency Imported condition classification; unverified.
Sodium: gradients, nutrient transport, fluid regulation and loss states (2026-09-17) · lines 967–978
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized masked trial in 53 infants born before 32 weeks · source_derived_draft · unverified_draft
### sodium-preterm-sodium Supplemented preterm infants had fewer recorded serum sodium values below 135 mmol/L. Condition category: nutrient_deficiency nutrient_topic: Sodium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Very premature infants can need a different sodium provision than older children or adults. organism: Human preterm infants tissue_or_cell_type: Whole-body growth and serum sodium experimental_model: Randomized masked trial in 53 infants born before 32 weeks limitations: Study regimen, not a dosing recommendation. Small neonatal trial; improved weight gain is not proof that every blood sodium measurement diagnoses total-body depletion. exposure: 4 mEq/kg/day supplemental sodium versus placebo, days 7–35 evidence_span: {"source_cache": "artifacts/sodium-research/25406227.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339", "start_char": 0, "end_char": 1645, "text_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339"} [sodium-p25406227] Impact of Early Sodium Supplementation on Hyponatremia and Growth in Premature Infants: A Randomized Controlled Trial. (2016). https://pubmed.ncbi.nlm.nih.gov/25406227/ DOI: 10.1177/0148607114558303
Complete structured claim and evidenceMean weight-gain velocity was 26.9 versus 22.9 g/kg/day with supplementation versus placebo.
Experimental context and source evidence
- availability_state
- nutrient_deficiency Imported condition classification; unverified.
- evidence_span
- {"source_cache": "artifacts/sodium-research/25406227.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339", "start_char": 0, "end_char": 1645, "text_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339"}
- experimental_model
- Randomized masked trial in 53 infants born before 32 weeks
- exposure
- 4 mEq/kg/day supplemental sodium versus placebo, days 7–35
- limitations
- Study regimen, not a dosing recommendation. Small neonatal trial; improved weight gain is not proof that every blood sodium measurement diagnoses total-body depletion.
- nutrient_topic
- Sodium research collection; topical membership is not evidence of a direct dietary effect. · Sodium
- organism
- Human preterm infants
- plain_language
- The sodium intervention improved weight gain in this small preterm-infant trial.
- primary_references
- [sodium-p25406227] Impact of Early Sodium Supplementation on Hyponatremia and Growth in Premature Infants: A Randomized Controlled Trial. (2016). https://pubmed.ncbi.nlm.nih.gov/25406227/ DOI: 10.1177/0148607114558303
- tissue_or_cell_type
- Whole-body growth and serum sodium
- trigger_kind
- nutrient_deficiency Imported condition classification; unverified.
Sodium: gradients, nutrient transport, fluid regulation and loss states (2026-09-17) · lines 980–991
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized masked trial in 53 infants born before 32 weeks · source_derived_draft · unverified_draft
### sodium-preterm-weight Mean weight-gain velocity was 26.9 versus 22.9 g/kg/day with supplementation versus placebo. Condition category: nutrient_deficiency nutrient_topic: Sodium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The sodium intervention improved weight gain in this small preterm-infant trial. organism: Human preterm infants tissue_or_cell_type: Whole-body growth and serum sodium experimental_model: Randomized masked trial in 53 infants born before 32 weeks limitations: Study regimen, not a dosing recommendation. Small neonatal trial; improved weight gain is not proof that every blood sodium measurement diagnoses total-body depletion. exposure: 4 mEq/kg/day supplemental sodium versus placebo, days 7–35 evidence_span: {"source_cache": "artifacts/sodium-research/25406227.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339", "start_char": 0, "end_char": 1645, "text_sha256": "a3c6cd28e4896dc8cdaeaacb7d524c55098b87dd5bf9d028ce49ba544832e339"} [sodium-p25406227] Impact of Early Sodium Supplementation on Hyponatremia and Growth in Premature Infants: A Randomized Controlled Trial. (2016). https://pubmed.ncbi.nlm.nih.gov/25406227/ DOI: 10.1177/0148607114558303
Complete structured claim and evidence
Where it participates (unsigned role)
Plasma aldosterone in combined Na/Mg-restricted mice was not higher than with normal diet, although sodium restriction alone increased it.
Experimental context and source evidence
- availability_state
- nutrient_deficiency Imported condition classification; unverified.
- cross_nutrient
- magnesium -> sodium -> potassium
- experimental_model
- Dietary restriction in C57BL/6J mice with renal transport assays
- limitations
- Unchanged concentration does not imply absent mineralocorticoid action or exclude other ENaC regulators.
- nutrient_topic
- Magnesium research collection; topical membership is not evidence of a direct dietary effect. · Magnesium
- organism
- Mus musculus
- plain_language
- The potassium loss pattern did not require a measured rise in circulating aldosterone in this experiment.
- primary_references
- [maeoka-2025-enac-romk] Hypomagnesaemia-associated hypokalaemia requires activation of both ENaC and ROMK (2025). https://pubmed.ncbi.nlm.nih.gov/41137719/ DOI: 10.1113/JP287704
- tissue_or_cell_type
- Kidney distal nephron
- trigger_kind
- nutrient_deficiency Imported condition classification; unverified.
Magnesium: cross-nutrient mechanisms and deficiency (2026-09-17) · lines 191–201
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Dietary restriction in C57BL/6J mice with renal transport assays · source_derived_draft · unverified_draft
### combined-na-mg-restriction-aldosterone-not-elevated Plasma aldosterone in combined Na/Mg-restricted mice was not higher than with normal diet, although sodium restriction alone increased it. Condition category: nutrient_deficiency nutrient_topic: Magnesium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The potassium loss pattern did not require a measured rise in circulating aldosterone in this experiment. organism: Mus musculus tissue_or_cell_type: Kidney distal nephron experimental_model: Dietary restriction in C57BL/6J mice with renal transport assays limitations: Unchanged concentration does not imply absent mineralocorticoid action or exclude other ENaC regulators. cross_nutrient: magnesium -> sodium -> potassium [maeoka-2025-enac-romk] Hypomagnesaemia-associated hypokalaemia requires activation of both ENaC and ROMK (2025). https://pubmed.ncbi.nlm.nih.gov/41137719/ DOI: 10.1113/JP287704
Complete structured claim and evidenceCombined Na/Mg restriction increased native ROMK activity in DCT2/CNT and lowered plasma K, while ENaC cleavage markers were preserved relative to normal diet.
Experimental context and source evidence
- availability_state
- nutrient_deficiency Imported condition classification; unverified.
- cross_nutrient
- magnesium -> sodium -> potassium
- duration
- Seven days
- experimental_contrast
- {"combination": "joint", "comparator": "Normal diet", "conditions": [{"entity_slug": "sodium", "state": "Restricted"}, {"entity_slug": "magnesium", "state": "Restricted"}], "effect_direction": "increase", "endpoint": "Native ROMK activity in DCT2/CNT", "intervention": "Combined dietary sodium and magnesium restriction"} Primary abstract PMID 41137719 / DOI 10.1113/JP287704 rechecked 2026-09-20. This comparison must not be separated into two single-deficiency effects.
- experimental_model
- Dietary restriction in C57BL/6J mice with renal transport assays
- limitations
- Co-occurrence supports the proposed mechanism; intracellular Mg and distal Na delivery were not directly measured.
- nutrient_topic
- Magnesium research collection; topical membership is not evidence of a direct dietary effect. · Magnesium
- organism
- Mus musculus
- plain_language
- In this combined shortage, the Mg-sensitive potassium pathway was more active while the sodium pathway that supports potassium exit remained available.
- primary_references
- [maeoka-2025-enac-romk] Hypomagnesaemia-associated hypokalaemia requires activation of both ENaC and ROMK (2025). https://pubmed.ncbi.nlm.nih.gov/41137719/ DOI: 10.1113/JP287704
- tissue_or_cell_type
- Kidney distal nephron
- trigger_kind
- nutrient_deficiency Imported condition classification; unverified.
Magnesium: cross-nutrient mechanisms and deficiency (2026-09-17) · lines 178–189
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Dietary restriction in C57BL/6J mice with renal transport assays · source_derived_draft · unverified_draft
### combined-na-mg-restriction-romk-hypokalemia Combined Na/Mg restriction increased native ROMK activity in DCT2/CNT and lowered plasma K, while ENaC cleavage markers were preserved relative to normal diet. Condition category: nutrient_deficiency nutrient_topic: Magnesium research collection; topical membership is not evidence of a direct dietary effect. plain_language: In this combined shortage, the Mg-sensitive potassium pathway was more active while the sodium pathway that supports potassium exit remained available. organism: Mus musculus tissue_or_cell_type: Kidney distal nephron experimental_model: Dietary restriction in C57BL/6J mice with renal transport assays limitations: Co-occurrence supports the proposed mechanism; intracellular Mg and distal Na delivery were not directly measured. cross_nutrient: magnesium -> sodium -> potassium duration: Seven days [maeoka-2025-enac-romk] Hypomagnesaemia-associated hypokalaemia requires activation of both ENaC and ROMK (2025). https://pubmed.ncbi.nlm.nih.gov/41137719/ DOI: 10.1113/JP287704
Complete structured claim and evidencePotassium supplementation reduced 24-hour pressure by approximately 3.9/1.6 mmHg under controlled feeding.
Experimental context and source evidence
- experimental_model
- Four-week crossover; 36 completers.
- limitations
- Untreated elevated-pressure adults with relatively low baseline sodium/potassium intake; no detected pulse-wave-velocity benefit.
- nutrient_topic
- Potassium research collection; topical membership is not evidence of a direct dietary effect. · Potassium
- organism
- Homo sapiens
- plain_language
- The blood-pressure effect was measured directly in this trial.
- primary_references
- [k-gijsbers2015-bp] Effects of sodium and potassium supplementation on blood pressure and arterial stiffness: a fully controlled dietary intervention study (2015). https://pubmed.ncbi.nlm.nih.gov/25673113/ DOI: 10.1038/jhh.2015.3
- tissue_or_cell_type
- Systemic circulation
Potassium: cross-nutrient mechanisms and deficiency (2026-09-17) · lines 1546–1555
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Four-week crossover; 36 completers. · source_derived_draft · unverified_draft
### k-controlled-feeding-pressure Potassium supplementation reduced 24-hour pressure by approximately 3.9/1.6 mmHg under controlled feeding. Condition category: normal nutrient_topic: Potassium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The blood-pressure effect was measured directly in this trial. organism: Homo sapiens tissue_or_cell_type: Systemic circulation experimental_model: Four-week crossover; 36 completers. limitations: Untreated elevated-pressure adults with relatively low baseline sodium/potassium intake; no detected pulse-wave-velocity benefit. [k-gijsbers2015-bp] Effects of sodium and potassium supplementation on blood pressure and arterial stiffness: a fully controlled dietary intervention study (2015). https://pubmed.ncbi.nlm.nih.gov/25673113/ DOI: 10.1038/jhh.2015.3
Complete structured claim and evidenceRat NIS expressed in Xenopus oocytes transported iodide with two sodium ions per anion and generated inward electrogenic transport.
Experimental context and source evidence
- cross_nutrient
- true
- experimental_model
- Rat NIS expressed in Xenopus laevis oocytes; electrophysiology and tracer uptake
- exposure
- Tracer uptake and electrophysiology; apparent sodium affinity 28 ± 3 mM and iodide affinity 33 ± 9 micromolar.
- limitations
- Rat-protein assay parameters are not dietary sodium requirements or human iodide thresholds.
- nutrient_topic
- Iodine research collection; topical membership is not evidence of a direct dietary effect. · Iodine
- organism
- Rat protein in Xenopus laevis oocytes
- plain_language
- NIS uses sodium movement to carry iodide into cells.
- primary_references
- [iodine-trans-stoichiometry1997] Thyroid Na+/I- symporter. Mechanism, stoichiometry, and specificity. (1997). https://pubmed.ncbi.nlm.nih.gov/9341168/ DOI: 10.1074/jbc.272.43.27230
- tissue_or_cell_type
- Oocyte plasma membrane
Iodine: thyroid hormone production, deficiency, excess and nutrient interactions (2026-09-17) · lines 167–178
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Rat NIS expressed in Xenopus laevis oocytes; electrophysiology and tracer uptake · source_derived_draft · unverified_draft
### iodine-trans-sodium-coupling Rat NIS expressed in Xenopus oocytes transported iodide with two sodium ions per anion and generated inward electrogenic transport. Condition category: normal nutrient_topic: Iodine research collection; topical membership is not evidence of a direct dietary effect. plain_language: NIS uses sodium movement to carry iodide into cells. organism: Rat protein in Xenopus laevis oocytes tissue_or_cell_type: Oocyte plasma membrane experimental_model: Rat NIS expressed in Xenopus laevis oocytes; electrophysiology and tracer uptake limitations: Rat-protein assay parameters are not dietary sodium requirements or human iodide thresholds. exposure: Tracer uptake and electrophysiology; apparent sodium affinity 28 ± 3 mM and iodide affinity 33 ± 9 micromolar. cross_nutrient: true [iodine-trans-stoichiometry1997] Thyroid Na+/I- symporter. Mechanism, stoichiometry, and specificity. (1997). https://pubmed.ncbi.nlm.nih.gov/9341168/ DOI: 10.1074/jbc.272.43.27230
Complete structured claim and evidencePectin increased sodium output in ileal effluent.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/pectin-research/6307932.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "fd45607a7ff1d1a20dd52d145134da591847919c3db47ef8a8cf5693fb9f80a1", "start_char": 0, "end_char": 1593, "text_sha256": "fd45607a7ff1d1a20dd52d145134da591847919c3db47ef8a8cf5693fb9f80a1"}
- experimental_model
- Within-person ileostomy balance study; six participants
- exposure
- 15 g/day citrus pectin on days 5-7 of a 10-day low-fiber feeding protocol
- limitations
- Ileal apparent absorption and output are not whole-body status or clinical deficiency; the colon was bypassed.
- nutrient_topic
- Pectin research collection; topical membership is not evidence of a direct dietary effect. · Pectin, structurally heterogeneous plant polysaccharides
- organism
- Homo sapiens
- plain_language
- More sodium left through the ileostomy; this is not proof of low blood sodium.
- primary_references
- [pectin-p6307932] The effect of citrus pectin on the absorption of nutrients in the small intestine. (1983). https://pubmed.ncbi.nlm.nih.gov/6307932/
- tissue_or_cell_type
- Small intestine; ileal effluent
Pectin: metabolism, signaling and nutrient connections (2026-09-17) · lines 555–566
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Within-person ileostomy balance study; six participants · source_derived_draft · unverified_draft
### pectin-ileal-sodium Pectin increased sodium output in ileal effluent. Condition category: normal nutrient_topic: Pectin research collection; topical membership is not evidence of a direct dietary effect. plain_language: More sodium left through the ileostomy; this is not proof of low blood sodium. organism: Homo sapiens tissue_or_cell_type: Small intestine; ileal effluent experimental_model: Within-person ileostomy balance study; six participants limitations: Ileal apparent absorption and output are not whole-body status or clinical deficiency; the colon was bypassed. exposure: 15 g/day citrus pectin on days 5-7 of a 10-day low-fiber feeding protocol evidence_span: {"source_cache": "artifacts/pectin-research/6307932.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "fd45607a7ff1d1a20dd52d145134da591847919c3db47ef8a8cf5693fb9f80a1", "start_char": 0, "end_char": 1593, "text_sha256": "fd45607a7ff1d1a20dd52d145134da591847919c3db47ef8a8cf5693fb9f80a1"} [pectin-p6307932] The effect of citrus pectin on the absorption of nutrients in the small intestine. (1983). https://pubmed.ncbi.nlm.nih.gov/6307932/
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