Cited by 162Regulation of Appetite and ObesityAdipokines, Inflammation, and Metabolic DiseasesHypothalamic control of reproductive hormones

The DOI matches its Crossref record; 165 of the 165 references it cites were found in a registry or an index.

Selective leptin resistance revisited

Open access
Mark, Allyn L.·2013·American Journal of Physiology-Regulatory, Integrative and Comparative Physiology

Abstract

In addition to effects on appetite and metabolism, leptin influences many neuroendocrine and physiological systems, including the sympathetic nervous system. Building on my Carl Ludwig Lecture of the American Physiological Society, I review the sympathetic and cardiovascular actions of leptin. The review focuses on a critical analysis of the concept of selective leptin resistance (SLR) and the role of leptin in the pathogenesis of obesity-induced hypertension in both experimental animals and humans. We introduced the concept of SLR in 2002 to explain how leptin might increase blood pressure (BP) in obese states, such as diet-induced obesity (DIO), that are accompanied by partial leptin resistance. This concept, analogous to selective insulin resistance in the metabolic syndrome, holds that in several genetic and acquired models of obesity, there is preservation of the renal sympathetic and pressor actions of leptin despite attenuation of the appetite and weight-reducing actions. Two potential overlapping mechanisms of SLR are reviewed: 1) differential leptin molecular signaling pathways that mediate selective as opposed to universal leptin action and 2) brain site-specific leptin action and resistance. Although the phenomenon of SLR in DIO has so far focused on preservation of sympathetic and BP actions of leptin, consideration should be given to the possibility that this concept may extend to preservation of other actions of leptin. Finally, I review perplexing data on the effects of leptin on sympathetic activity and BP in humans and its role in human obesity-induced hypertension.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1152/ajpregu.00180.2013

Cites

165 of 165 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

1 retracted

Show all 165 references

Research works printed but not linked: 3

  1. Landsberg L, 1986, Q J Med, 61, 1081
  2. Rosmond R, 2000, J Clin Endocrinol Metab, 85, 3126
  3. Tanida M, 2003, In Vivo, 17, 213

Cited by

Sorted by citations

See all 162

Metadata

Authors
Mark, A. L.
Affiliations
University of Iowa (US)
Corresponding author
Mark, Allyn L.
Venue
American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
Published
2013-09-15
Volume
305
Issue
6
Pages
R566-R581
ISSN
  • 0363-6119 (ISSN-L)
  • 1522-1490
OpenAlex
W2064109637
Cited by
162
References
165
Citations by year
2026: 7 · 2025: 4 · 2024: 12 · 2023: 6 · 2022: 6 · 2021: 16 · 2020: 13 · 2019: 12 · 2018: 11 · 2017: 14 · 2016: 17 · 2015: 19 · 2014: 22 · 2013: 3
FWCI
2.45
Type
journal article
Language
en
Open access
Locations
  • American Journal of Physiology-Regulatory, Integrative and Comparative Physiology (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5p50hl044546-05)
  • National Heart, Lung, and Blood Institute (HL-55006, HL-96571, R01HL063887, HL-63887, HL-14388, HL-84207, HL-44546, P50HL055006, P01HL014388, P01HL084207, P01HL096571)
Topics
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
  • Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
Keywords
leptin, obesity-related hypertension, diet-induced obesity, sympathetic nervous system, blood pressure regulation, leptin signaling, appetite regulation
MeSH terms
Animals, Brain, Humans, Hypertension, Myocardium, Obesity, Sympathetic Nervous System, Leptin

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review