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Receptor Mechanisms (PHAR0012)

Key information

Faculty
Faculty of Life Sciences
Teaching department
Division of Biosciences
Credit value
15
Restrictions
Co or pre-requisite: normally, students will also be taking or have taken PHAR0011 Molecular Pharmacology.
Timetable

Alternative credit options

There are no alternative credit options available for this module.

Description

This module builds on the material covered in PHAR0011 Molecular Pharmacology. It covers the mechanisms involved in the generation of a response following receptor activation, either by a natural hormone or neurotransmitter or by drug action, and how drugs may interfere with receptor-mediated responses.Ìý

Mechanisms involving ligand-gated ion channels, voltage-dependent sodium, calcium and potassium channels, G-proteins, second messengers (e.g. inositol phosphates, cAMP) and cellular kinases are then considered in detail, together with the role of calcium. The material is supplemented by group presentations and discussion of selected research papers related to the core lectures and by the preparation of an essay (Level-6 students) or data interpretation exercise (Level-7 students).Ìý

On completion of the module, students should be able to demonstrate critical understanding of the following topics:Ìý

1) Mechanism of action of G-protein coupled receptors.Ìý

2) Secondary messengers: Ca2+, Ìýinositol phosphates, cAMP and protein kinasesÌý

3) Ligand gated ion channel receptor mechanisms.Ìý

4) Voltage-gated ion channel structure and function.Ìý

This module is an option for students in BSc/MSci Pharmacology and related degree programmes (including Neuroscience, and relevant streams of Biomedical and Natural Sciences) and postgraduate students studying MSc Biomedical Sciences or appropriate MRes programmes. It is assumed that students taking this module will have studied aspects of physiology and biochemistry for at least two years at University level. It is normally a pre-requisite that students taking this module will have also or be studying PHAR0011: Molecular Pharmacology.Ìý

Indicative lecture list (based on 2023/24 syllabus)Ìý

Receptor DesensitisationÌý

LGIC Receptor Mechanisms and Synaptic CurrentsÌý

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NMDA receptor activationÌý

Receptor traffickingÌý

GPCR Desensitisation and Trafficking (2 lectures)Ìý

Receptor Tyrosine Kinase and G Proteins (2 lectures)Ìý

Structure and Function of Voltage-dependent Sodium and Calcium Channels (2 lectures)

Potassium Channel Structure and Function (3 lectures)Ìý

G-Protein Modulation of K-ChannelsÌý

PIP2 Regulation of M-Type K-ChannelsÌý

IP3 and Ca2+ SignallingÌý

cAMP dependent Signalling (2 lectures)Ìý

Inositol Lipids – Cell Signalling (2 lectures)Ìý

Module deliveries for 2024/25 academic year

Intended teaching term: Term 1 ÌýÌýÌý Undergraduate (FHEQ Level 6)

Teaching and assessment

Mode of study
In person
Methods of assessment
85% Fixed-time remote activity
15% Coursework
Mark scheme
Numeric Marks

The methods of assessment for affiliate students may be different to those indicated above. Please contact the department for more information.

Other information

Number of students on module in previous year
29
Module leader
Professor Alasdair Gibb
Who to contact for more information
a.gibb@ucl.ac.uk

Intended teaching term: Term 1 ÌýÌýÌý Undergraduate (FHEQ Level 7)

Teaching and assessment

Mode of study
In person
Methods of assessment
85% Fixed-time remote activity
15% Coursework
Mark scheme
Numeric Marks

Other information

Number of students on module in previous year
6
Module leader
Professor Alasdair Gibb
Who to contact for more information
a.gibb@ucl.ac.uk

Intended teaching term: Term 1 ÌýÌýÌý Postgraduate (FHEQ Level 7)

Teaching and assessment

Mode of study
In person
Methods of assessment
85% Fixed-time remote activity
15% Coursework
Mark scheme
Numeric Marks

Other information

Number of students on module in previous year
4
Module leader
Professor Alasdair Gibb
Who to contact for more information
a.gibb@ucl.ac.uk

Last updated

This module description was last updated on 8th April 2024.

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