Evidence map›Paper›PMID 24759771›Full record

ArticleNeuroscience2014

Differences in carbachol dose, pain condition, and sex following lateral hypothalamic stimulation.

J E Holden, E Wang, J R Moes, M Wagner, A Maduko, Y Jeong

Abstract read
In one paragraph

Article in Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

J E HoldenThe University of Michigan School of Nursing, 400 N. Ingalls Building, Ann Arbor, MI 48109-5482, United States; College of Nursing Science, Kyung Hee University, 26 Kyunghee-daero, Dongdaemun-gu, Seoul 130-701, Republic of Korea. Electronic address: holdenje@umich.edu.
E WangUniversity of Illinois at Chicago, College of Applied Health Sciences, 1919 W. Taylor Street, Chicago, IL 60612, United States. Electronic address: chewang@uic.edu.
J R MoesCalvin College Nursing Department, Science Building Room 245, 1734 Knollcrest Circle SE, Grand Rapids, MI, United States. Electronic address: jrm3@calvin.edu.
M WagnerThe University of Michigan School of Nursing, 400 N. Ingalls Building, Ann Arbor, MI 48109-5482, United States. Electronic address: mawag@umich.edu.
A MadukoThe University of Michigan School of Nursing, 400 N. Ingalls Building, Ann Arbor, MI 48109-5482, United States. Electronic address: amaduko@umich.edu.
Y JeongCollege of Nursing Science, Kyung Hee University, 26 Kyunghee-daero, Dongdaemun-gu, Seoul 130-701, Republic of Korea. Electronic address: yjeong2@khu.ac.kr.
University of Michigan–Ann Arbor · USCalvin University · USKyung Hee University · KRUniversity of Illinois Chicago · US

Funding

NEUROBIOLOGY OF HYPOTHALAMIC PAIN MODULATIONR01NR004778 · NINR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOLDEN, JANEAN E · 1999 to 2012
$3.0M
Posterior hypothalamic modulation of painR01NR013861 · NINR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOLDEN, JANEAN E · 2012 to 2016
$1.9M
NINR NIH HHS NR04778NINR NIH HHS R01 NR004778NINR NIH HHS R01 NR013861
6 · The paper itself

Abstract

Lateral hypothalamic (LH) stimulation produces antinociception in female rats in acute, nociceptive pain. Whether this effect occurs in neuropathic pain or whether male-female sex differences exist is unknown. We examined the effect of LH stimulation in male and female rats using conditions of nociceptive and neuropathic pain. Neuropathic groups received chronic constriction injury (CCI) to induce thermal hyperalgesia, a sign of neuropathic pain. Nociceptive rats were naive for CCI, but received the same thermal stimulus following LH stimulation. To demonstrate that CCI ligation produced thermal hyperalgesia, males and females received either ligation or sham surgery for control. Both males and females demonstrated significant thermal hyperalgesia following CCI ligation (p<0.05), but male sham surgery rats also showed a significant left-right difference not present in female sham rats. In the second experiment, rats randomly assigned to CCI or nociceptive groups were given one of three doses of the cholinergic agonist carbachol (125, 250, or 500 nmol) or normal saline for control, microinjected into the left LH. Paw withdrawal from a thermal stimulus (paw withdrawal latency; PWL) was measured every 5 min for 45 min. Linear mixed models analysis showed that males and females in both pain conditions demonstrated significant antinociception, with the 500-nmol dose producing the greatest effect across groups compared with controls for the left paw (p<0.05). Female CCI rats showed equivalent responses to the three doses, while male CCI rats showed more variability for dose. However, nociceptive females responded only to the 500-nmol dose, while nociceptive males responded to all doses (p<0.05). For right PWL, only nociceptive males showed a significant carbachol dose response. These findings are suggestive that LH stimulation produces antinociception in male and female rats in both nociceptive and neuropathic pain, but dose response differences exist based on sex and pain condition.

Indexed as

Sex CharacteristicsAnalgesics, Non-NarcoticAnimalsBlood PressureBody TemperatureCarbacholCholinergic AgonistsDose-Response Relationship, DrugEstrous CycleFemaleFunctional LateralityHeart RateHot TemperatureHyperalgesiaHypothalamic Area, LateralMaleAnalgesics, Non-NarcoticCarbacholCholinergic Agonistsanalgesiaantinociceptionlateral hypothalamusnociceptionsex differences

Identifiers

PMID24759771
PMCPMC6025747
OpenAlexW2028044292

What OpenQuestion holds

Textmetadata
LicenceTDM
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.