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Drugs of Abuse, Immunomodulation, and Aids

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Cover of 'Drugs of Abuse, Immunomodulation, and Aids'

Table of Contents

  1. Altmetric Badge
    Book Overview
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    Chapter 1 Cellular Mechanisms Involved in the Modulation of the Immune System by Drugs of Abuse
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    Chapter 2 Immunomodulation of Macrophage Functions by Opioids
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    Chapter 3 Morphine Accelerates the Progression of Sepsis in an Experimental Sepsis Model
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    Chapter 4 Morphine Depresses Macrophage Numbers and Function in Mouse Spleens
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    Chapter 5 Centrally-Mediated Opioid-Induced Immunosuppression
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    Chapter 6 The Expression of Interleukin-1β Converting Enzyme (ICE) in Rat is Decreased Following Chronic Exposure to Morphine
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    Chapter 7 Opioid Receptor Gene Expression in the Porcine Immune System
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    Chapter 8 The Effects of Interaction Between Morphine and Interleukin-1 on the Immune Response
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    Chapter 9 Morphine Alters the Immune Response to Influenza Virus Infection in Lewis Rats
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    Chapter 10 Orphan Opioid Receptor Oligonucleotides Inhibit HIV-1 Expression in Human Brain Cells
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    Chapter 11 Opiate Effects on In Vitro Human Retroviral Infection
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    Chapter 12 FIV
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    Chapter 13 Changes in Kappa Opioid Receptor Expression During Maturation of Mouse Lymphocytes
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    Chapter 14 Modulation of DPK Cell Function by the Kappa Opioid Agonist U50,488H
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    Chapter 15 Properties of µ3 Opiate Alkaloid Receptors in Macrophages, Astrocytes, and HL-60 Human Promyelocytic Leukemia Cells
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    Chapter 16 Morphine During Pregnancy in the Rat
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    Chapter 17 Western Blot Analysis of the Delta (δ)-Opioid Receptor in Activated Murine T Cells
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    Chapter 18 Morphine’s Immunologic and Analgesic Effects
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    Chapter 19 Immunomodulation Mediated by Microinjection of Morphine into the Periaqueductal Gray Matter of the Mesencephalon
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    Chapter 20 Novel Non-Peptidic Opioid Compounds with Immunopotentiating Effects
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    Chapter 21 Cocaine-Induced Release of Corticosterone Mediates Differential Effects on T-Helper1 and T-Helper2 Cell Responses
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    Chapter 22 Cocaine Enhances Monocyte Migration Across the Blood-Brain Barrier
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    Chapter 23 The role of macrophages in THC-induced alteration of the cytokine network.
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    Chapter 24 Cannabinoid receptors and the cytokine network.
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    Chapter 25 Cannabinoid Receptor Agonists Enhance Syncytia Formation in MT-2 Cells Infected with Cell Free HIV-1MN
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    Chapter 26 Cannabinoids Alter Neurotoxicity Produced by Interleukin-6 in Central Nervous System Neurons
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    Chapter 27 Viral and Host Determinants of Neurovirulence of HIV-1 Infection
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    Chapter 28 Immunity and Prenatal Alcohol Exposure
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    Chapter 29 Isobutyl Nitrite Liberates Nitric Oxide Which is not Responsible for the Immunotoxicity of the Inhalant
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    Chapter 30 The Role of Norepinephrine and Beta-2-Adrenergic Receptor Stimulation in the Modulation of Th1, Th2, and B Lymphocyte Function
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    Chapter 31 Nicotine-Induced Modulation of T Cell Function
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    Chapter 32 Regulated Expression of an Endopeptidase that Hydrolyses β-Endorphin During Differentiation of Macrophages and T Cells
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    Chapter 33 Cytokine Induction During Methionine Enkephalin and AZT Therapy for Murine Retrovirus Infection
Attention for Chapter 24: Cannabinoid receptors and the cytokine network.
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Chapter title
Cannabinoid receptors and the cytokine network.
Chapter number 24
Book title
Drugs of Abuse, Immunomodulation, and Aids
Published in
Advances in experimental medicine and biology, January 1998
DOI 10.1007/978-1-4615-5347-2_24
Pubmed ID
Book ISBNs
978-1-4613-7439-8, 978-1-4615-5347-2
Authors

T W Klein, C Newton, H Friedman, Klein, Thomas W., Newton, Catherine, Friedman, Herman, Thomas W. Klein, Catherine Newton, Herman Friedman

Abstract

Splenocyte cultures from BALB/c mice were treated with THC and mitogen and shown to produce less Th1 cytokine, IFN gamma, and more Th2 cytokines, IL-4 and IL-10. This suggested that drug treatment caused a shift in the development of Th1 and Th2 cells. In studies designed to look at molecular mechanisms, the CBI antagonist, SR141716A, did not attenuate the THC enhancement of IL-4 production, but pertussis toxin attenuated the drug effect and the CB2 agonist, JWH-051, increased IL-4 production similar to THC. These results suggest that cannabinoids may increase Th2 development and IL-4 production in cultured immune cells through the activity of the CB2 receptor subtype. Studies are currently in progress to further define the molecular and cellular mechanisms involved.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 3 30%
Student > Bachelor 2 20%
Student > Ph. D. Student 2 20%
Other 1 10%
Professor > Associate Professor 1 10%
Other 0 0%
Unknown 1 10%
Readers by discipline Count As %
Agricultural and Biological Sciences 3 30%
Pharmacology, Toxicology and Pharmaceutical Science 2 20%
Biochemistry, Genetics and Molecular Biology 1 10%
Medicine and Dentistry 1 10%
Neuroscience 1 10%
Other 0 0%
Unknown 2 20%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 3. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 24 December 2021.
All research outputs
#7,444,500
of 22,757,090 outputs
Outputs from Advances in experimental medicine and biology
#1,226
of 4,926 outputs
Outputs of similar age
#19,463
of 93,763 outputs
Outputs of similar age from Advances in experimental medicine and biology
#11
of 34 outputs
Altmetric has tracked 22,757,090 research outputs across all sources so far. This one is in the 44th percentile – i.e., 44% of other outputs scored the same or lower than it.
So far Altmetric has tracked 4,926 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 6.0. This one has gotten more attention than average, scoring higher than 65% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 93,763 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 18th percentile – i.e., 18% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 34 others from the same source and published within six weeks on either side of this one. This one is in the 29th percentile – i.e., 29% of its contemporaries scored the same or lower than it.