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Chapter 5: Problem 10

Which molecules do not possess immunosuppressive properties? a. free cortisol b. IL-1 receptor antagonist c. substance \(P\) d. rhodopsin e. vasoactive intestinal peptide

Short Answer

Expert verified
a. Free cortisol b. Interleukin-1 (IL-1) receptor antagonist c. Substance P d. Rhodopsin e. Vasoactive Intestinal Peptide (VIP) Answer: c. Substance P and d. Rhodopsin

Step by step solution

01

Definition of immunosuppressive properties

Immunosuppressive properties refer to the ability of certain molecules to suppress or weaken the immune system. Identifying the molecules with immunosuppressive properties requires knowledge about each of the given molecules and their function in the immune system.
02

Analyzing the options

Here is a brief description and analysis for each of the options: a. Free cortisol: Known as a stress hormone, cortisol has immunosuppressive effects because it can reduce inflammation and inhibit the action of certain immune cells. Therefore, free cortisol possesses immunosuppressive properties. b. Interleukin-1 (IL-1) receptor antagonist: As an antagonist to IL-1 receptor, it blocks the pro-inflammatory cytokine IL-1 and plays a role in controlling inflammation. Although it has anti-inflammatory properties, its primary effect is not immunosuppression, making it a candidate for the answer. c. Substance P: A neuropeptide involved in transmitting pain signals to the brain, it does not have a known immunosuppressive function. d. Rhodopsin: A light-sensitive receptor protein found in the retina, it has no known relationship to the immune system or immunosuppressive properties. e. Vasoactive Intestinal Peptide (VIP): VIP has known immunosuppressive effects, such as inhibiting the production of pro-inflammatory cytokines and promoting an anti-inflammatory response.
03

Identifying the correct answer

Based on the analysis of each option, the correct answer is: Which molecules do not possess immunosuppressive properties? c. Substance P d. Rhodopsin Substance P and Rhodopsin do not have known immunosuppressive properties, as they serve different functions related to pain transmission and light detection, respectively.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Neuroimmune Pharmacology
Neuroimmune pharmacology explores the complex interactions between the nervous system, immune system, and drugs. This field combines principles from neuroscience, immunology, and pharmacology to understand how drugs affect neuroimmune communication. For example, certain medications can target neurotransmitters and neuropeptides, like substance P, which is known to transmit pain signals rather than suppress immune function.

This distinction is crucial in education about drug development and therapy for diseases with a neuroimmune component, such as multiple sclerosis or rheumatoid arthritis. Understanding this helps students realize why not all neurotransmitters and neuropeptides possess immunosuppressive properties. Moreover, knowledge in this area aids in the identification of potential therapeutic targets for managing neurodegenerative or autoimmune disorders.
Cortisol and the Immune System
Cortisol, often termed the 'stress hormone', plays a multifaceted role in regulating the immune system. High levels of cortisol, particularly free cortisol, can suppress the immune response by inhibiting inflammation and the activity of various immune cells, such as T cells and macrophages.

In the context of immunosuppressive properties, cortisol's function in dampening immune responses is used therapeutically in conditions where the immune system is overly active, leading to inflammation and tissue damage. Despite its critical role, prolonged exposure to high cortisol levels due to chronic stress or long-term use of corticosteroids can lead to weakened immune defense and increased susceptibility to infections. This dichotomy underscores the importance of understanding the immune-modulating effects of cortisol in neuroimmune pharmacology and the education of healthcare professionals.
Cytokines and Inflammation
Cytokines are small proteins released by cells that have a significant impact on the communication between cells, playing a pivotal role in immune responses and inflammation. They can be pro-inflammatory, like interleukin-1 (IL-1), driving the immune response towards inflammation, or anti-inflammatory, serving to reduce inflammation and promote healing.

The IL-1 receptor antagonist is a naturally occurring inhibitor of the pro-inflammatory cytokine IL-1. By blocking IL-1, the antagonist can reduce inflammation but doesn't directly suppress the immune system – it regulates its response. IL-1 receptor antagonists can be used therapeutically in conditions characterized by excessive inflammation, such as auto-inflammatory syndromes. Understanding cytokine modulation is fundamental in developing anti-inflammatory therapies and forms a cornerstone of education in the area of immunopharmacology.

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Most popular questions from this chapter

Visual cortex occupies the following structures: a. occipital and parts of the parietal and temporal lobes of the cerebral cortex b. parietal and parts of occipital and temporal lobes of the cerebral cortex c. lateral geniculate body, occipital and frontal lobes of the cerebral cortex d. frontal and parts of occipital and temporal lobes of the cerebral cortex e. occipital and parts of frontal and parietal lobes of the cerebral cortex

Aqueous is produced by: a. ciliary epithelium b. corneal endothelium c. Schlemm's canal d. trabecular meshwork e. iris roots

Which statement is not true regarding immune privilege? a. The phenomenon of immune privilege was initially described in the nineteenth century. b. Immune privilege is defined as a prolonged, sometimes indefinite, survival of organ or tissue grafts at special body/organ sites. c. Immune privilege is a dynamic process maintained by anatomic structures and immunoregulatory forces. d. Grafts placed in immune privileged sites remain sequestered from the immune environment. e. Both active and passive factors of immune privileged sites and tissues contribute to the privileged status.

All the following is true about anterior chamber immune associated deviation (ACAID) except: a. ACAID is an antigen-specific systemic immune response to eye-derived antigens. b. ACAID is an actively acquired and actively maintained manifestation of ocular immune privilege. c. In ACAID aqueous humor possesses immunomodulatory properties and inhibits all immune reactions. d. ACAID is a form of peripheral tolerance, unlike central tolerance, where clonal deletion and/or anergy occur within the thymus. e. Once induced, ACAID persists for a very long period of time.

Which substance found in the eye is not uveitogenic? a. S-antigen (arrestin) b. TGF- \(\beta\) c. interphotoreceptor retinoid-binding protein (IRBP) d. recoverin e. phosduscin
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