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.

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.

Recorded relationships

What it acts on

  1. Low-sodium DASH versus high-sodium control produced mean systolic differences of 7.1 mmHg without hypertension and 11.5 mmHg with hypertension.

    Sodium → Arterial blood pressure source_derived_draftungraded
    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 evidence
  2. 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.

    Sodium → Arterial blood pressure source_derived_draftungraded
    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 evidence
  3. Length 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 evidence
  4. Supplemented preterm infants had fewer recorded serum sodium values below 135 mmol/L.

    Sodium → Plasma or serum sodium concentration source_derived_draftungraded
    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 evidence
  5. Mean weight-gain velocity was 26.9 versus 22.9 g/kg/day with supplementation versus placebo.

    Sodium → Preterm infant weight-gain velocity source_derived_draftungraded
    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)

  1. Plasma aldosterone in combined Na/Mg-restricted mice was not higher than with normal diet, although sodium restriction alone increased it.

    Magnesium → Aldosterone source_derived_draftungraded
    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 evidence
  2. 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.

    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 evidence
  3. Potassium supplementation reduced 24-hour pressure by approximately 3.9/1.6 mmHg under controlled feeding.

    Potassium → Arterial blood pressure source_derived_draftungraded
    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 evidence
  4. Rat 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 evidence
  5. Pectin 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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In the sources

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    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards