Evidence map›Paper›PMID 20304807›Full record

ArticleBlood2010

Pain-related behaviors and neurochemical alterations in mice expressing sickle hemoglobin: modulation by cannabinoids.

Divyanshoo R Kohli, Yunfang Li, Sergey G Khasabov, Pankaj Gupta, Lois J Kehl, Marna E Ericson, Julia Nguyen, Vinita Gupta, Robert P Hebbel, Donald A Simone and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

126 citing papers in PubMed, 1 synthesis or guideline pooled it, 182 citations in OpenAlex.

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  17. ΔThe Journal of pharmacology and experimental therapeutics · 2024
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66 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Divyanshoo R KohliVascular Biology Center, Division of Hematology, Oncology & Transplantation, Department of Medicine, University of Minnesota, Minneapolis 55455, USA.
Yunfang Li
Sergey G Khasabov
Pankaj Gupta
Lois J Kehl
Marna E Ericson
Julia Nguyen
Vinita Gupta
Robert P Hebbel
Donald A Simone
Kalpna Gupta
Center for Vascular Biology Research · USUniversity of Minnesota · USBio-Rad (United States) · USUniversity of Minnesota Medical Center · US

Funding

VASCULAR PATHOBIOLOGY OF SICKLE CELL DISEASEP01HL055552 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI HEBBEL, ROBERT P · 1995 to 2011
$17.3M
CANNABINOID MODULATION OF HYPERALGESIAR01DA011471 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SIMONE, DONALD · 2000 to 2014
$4.2M
Opioid Activity in Endothelium in Sickle Cell Disease R01HL068802 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI GUPTA, KALPNA · 2002 to 2012
$2.6M
Characteristics and mechanisms of pain in sickle cell diseaseR01HL103733 · NHLBI · UNIVERSITY OF MINNESOTA · PI GUPTA, KALPNA, SIMONE, DONALD · 2010 to 2014
$1.9M
NHLBI NIH HHS HL068802NHLBI NIH HHS HL55552NHLBI NIH HHS P01 HL055552NHLBI NIH HHS R01 HL068802NHLBI NIH HHS R01 HL103733NIDA NIH HHS DA011471NIDA NIH HHS R01 DA011471
6 · The paper itself

Abstract

Sickle cell disease causes severe pain. We examined pain-related behaviors, correlative neurochemical changes, and analgesic effects of morphine and cannabinoids in transgenic mice expressing human sickle hemoglobin (HbS). Paw withdrawal threshold and withdrawal latency (to mechanical and thermal stimuli, respectively) and grip force were lower in homozygous and hemizygous Berkley mice (BERK and hBERK1, respectively) compared with control mice expressing human hemoglobin A (HbA-BERK), indicating deep/musculoskeletal and cutaneous hyperalgesia. Peripheral nerves and blood vessels were structurally altered in BERK and hBERK1 skin, with decreased expression of mu opioid receptor and increased calcitonin gene-related peptide and substance P immunoreactivity. Activators of neuropathic and inflammatory pain (p38 mitogen-activated protein kinase, STAT3, and mitogen-activated protein kinase/extracellular signal-regulated kinase) showed increased phosphorylation, with accompanying increase in COX-2, interleukin-6, and Toll-like receptor 4 in the spinal cord of hBERK1 compared with HbA-BERK. These neurochemical changes in the periphery and spinal cord may contribute to hyperalgesia in mice expressing HbS. In BERK and hBERK1, hyperalgesia was markedly attenuated by morphine and cannabinoid receptor agonist CP 55940. We show that mice expressing HbS exhibit characteristics of pain observed in sickle cell disease patients, and neurochemical changes suggestive of nociceptor and glial activation. Importantly, cannabinoids attenuate pain in mice expressing HbS.

Indexed as

Anemia, Sickle CellAnimalsBehavior, AnimalCalcitonin Gene-Related PeptideCannabinoid Receptor AgonistsCannabinoidsCyclohexanolsDisease Models, AnimalFemaleHemoglobin, SickleHumansHyperalgesiaMaleMiceMice, KnockoutMice, Transgenic3-(2-hydroxy-4-(1,1-dimethylheptyl)phenyl)-4-(3-hydroxypropyl)cyclohexanolCalcitonin Gene-Related PeptideCannabinoid Receptor AgonistsCannabinoidsCyclohexanolsHemoglobin, SickleMorphineReceptors, Opioid, muRecombinant ProteinsSubstance P

Identifiers

PMID20304807
PMCPMC2913454
OpenAlexW2033626184

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.