The Alaafin of Oyo-elect, Oba Abimbola Owoade, is set to embark on a 21-day traditional rites as he prepares for his ascension to the throne.
The announcement of Owoade’s selection as the new monarch of the ancient Yoruba town was made by Oyo State Governor, Seyi Makinde, on Friday. On Monday, the governor officially presented him with the staff of office, marking the formal recognition of his new role.
Oba Owoade succeeds the late Alaafin, Oba Lamidi Adeyemi III, who passed away three years ago, leaving a significant void in the revered monarchy.
The presentation ceremony was attended by the kingmakers, known as the Oyomesi, alongside top government officials and notable personalities from across the state.
Following the event, an anonymous source informed PUNCH Online that the newly appointed Alaafin had left for Oyo town, where he is expected to be welcomed by the community. The source further disclosed that Oba Owoade will begin his mandatory 21-day traditional rites for his ascension to the throne immediately.
“Oba Owoade has traveled to Oyo town to meet with the sons and daughters of the town, and his 21-day traditional rites for his ascension to the throne will commence without delay,” the source said.
Introduction
Types of Steroids
Effects and Side Effects
History and Usage
# Contents
## Steroid
Steroids are a class of organic compounds characterized by a specific type of chemical structure.
They are primarily found in animals, plants, fungi, and some bacteria, where they play diverse roles in biological processes.
Steroids have three interconnected rings, with functional groups such as hydroxyl or ketone groups attached to
the molecule. Their structure is crucial for their activity, enabling them to act as hormones, vitamins, or other bioactive compounds.
## Page version status
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It has been reviewed and updated by experts in the field.
For more detailed information, please refer to the original
source materials.
## Nomenclature
The nomenclature of steroids refers to the systematic naming of these
compounds. Steroids are named based on their structural features or biological
functions. For example, “cholesterol” refers to a specific steroid molecule produced in the liver and
used in animal cell membranes. Other examples include “sex hormones,” such as estrogen and testosterone,
which are steroidal molecules involved in reproduction and endocrine regulation.
## Rings and functional groups
Steroids have a unique structure with three interconnected
rings. The core of the steroid framework consists of two cyclohexane
rings fused together, forming a bicyclic system. Functional groups,
such as hydroxyl (-OH) or ketone (C=O) groups, are attached to this framework and play a critical role in determining the biological activity of the
molecule. These functional groups can influence steroid behavior, such as their
affinity for specific receptors or their solubility in different
environments.
## Naming convention
The naming convention for steroids follows specific rules that help differentiate between the various types
of steroidal molecules. The name often includes a
prefix derived from the class of compounds (e.g.,
“sterol” for cholesterol, “keto” for ketone-containing sterols).
Additional suffixes may indicate modifications or functional groups present on the molecule.
This system ensures clarity and precision in communication within scientific communities.
## Species distribution
Steroids are distributed across a wide range of species.
Their presence is not limited to one type of organism, as they can be found in both eukaryotes and prokaryotes.
For example:
– **Eukaryotic organisms**: Steroids are abundant in animals, plants, fungi, and single-celled eukaryotes like protozoa.
– **Prokaryotic organisms**: Sterols, a type of steroid, are found
in bacterial cell membranes and play a role in maintaining membrane
integrity.
## Eukaryotic
In eukaryotic organisms, steroids serve various biological functions.
For instance:
– Animals produce a wide variety of steroids, including sex hormones (e.g.,
estrogen, testosterone) that regulate reproduction and metabolism.
– Plants synthesize sterols as part of their cell membranes, contributing to the
strength and structure of these cellular structures.
– Fungi also produce sterols, such as ergosterol, which is essential
for the integrity of fungal cell membranes.
## Prokaryotic
In prokaryotic organisms, sterols are a key component of bacterial cell membranes.
These sterols help maintain membrane fluidity and flexibility, ensuring that the cell can function under various environmental conditions.
While sterols are common in bacteria and archaea, they are
not typically found in other types of prokaryotes, such as viruses.
## Fungal
Fungi produce a variety of sterols, including ergosterol, which is a
fundamental component of fungal cell membranes.
Ergosterol’s structure differs slightly from cholesterol,
the primary sterol in animals, but it serves similar functions in maintaining membrane integrity and facilitating
the transport of ions and nutrients across the membrane.
## Plant
In plants, sterols are essential for the structural integrity of cellular membranes.
Unlike animals, plants do not synthesize cholesterol but instead produce a related molecule called phytosterol.
Phytosterols share some structural similarities with animal sterols but have unique features that
make them suited to plant biology. These compounds contribute to membrane stability and help regulate growth and development in plants.
## Animal
Animals are perhaps the most complex users of
steroids, producing a vast array of these molecules for various
purposes. For example:
– **Sex hormones**: Steroids such as testosterone (male) and
estrogen (female) play critical roles in reproduction and sexual differentiation.
– **Adrenal steroids**: The adrenal glands produce corticosteroids, which are involved in stress response
and immune function.
– **Vitamin D**: A steroid molecule derived from cholesterol that is essential for bone health and calcium absorption.
– **Other sterols**: Cholesterol itself is a vital component
of animal cell membranes and precursor to various hormones and other bioactive compounds.
## Types
Steroids can be categorized based on their function or
structure:
– **By function**: Sex steroids (e.g., estrogen, testosterone), adrenal steroids (e.g.,
cortisol), vitamin D derivatives, and sterols like cholesterol.
– **By structure**: Intact ring systems, cleaved rings, contracted rings,
or expanded rings.
## Rings and functional groups
The number and arrangement of rings in the steroid
framework influence its biological activity.
For example:
– **Intact ring system**: Steroids with all three rings intact often retain their basic structural features,
allowing them to interact with specific receptors and perform normal cellular functions.
– **Cleaved rings**: Modified steroids where one or more rings have
been broken or altered can result in compounds with different properties.
These derivatives may be more effective at targeting specific cellular pathways or receptors.
– **Contracted rings**: Steroids with one ring contracted into a smaller, often five-membered structure are
common in certain hormones and signaling molecules.
– **Expanded rings**: Some steroid derivatives have additional carbons added to the ring system,
altering their shape and function.
## Biological significance
Steroids are biologically significant compounds with diverse roles in organisms.
They serve as signaling molecules, hormone precursors, and structural components
of cell membranes. For example:
– **Signaling**: Steroids can act as hormones, transmitting signals within and
between cells to regulate gene expression and cellular
activity.
– **Vitamin D**: A steroid derivative that is essential for bone
health and calcium absorption.
– **Cholesterol**: A major component of animal cell membranes, which also serves as a precursor for sex hormones and other steroidal
molecules.
## Biosynthesis and metabolism
The biosynthesis of steroids involves complex biochemical pathways that convert simple precursors into highly
structured molecules. The two primary pathways for steroid synthesis are
the Mevalonate pathway (also known as the cholesterol
biosynthesis pathway) and the alternative pathways, such as the reverse transport of sterols in cells.
### Mevalonate pathway
The Mevalonate pathway is a series of enzymatic reactions that convert acetyl-CoA into mevalonic acid, which serves as a
precursor for the synthesis of cholesterol and other steroids.
This pathway is active in most animals and plays a critical role in maintaining cellular
health and homeostasis.
### Steroidogenesis
Steroidogenesis refers to the process by which sterols
are synthesized and modified into biologically active molecules.
For example, cholesterol can be converted into vitamin D in sunlight, or transformed into sex hormones like estrogen and testosterone.
This process is tightly regulated by the body to ensure that steroid levels remain within a healthy
range.
### Alternative pathways
In addition to the Mevalonate pathway, alternative pathways for steroid biosynthesis exist, particularly
in certain tissues and organisms. These pathways may involve different precursors or unique
enzymatic modifications, allowing for the production of specialized sterols tailored to specific
biological needs.
### Catabolism and excretion
Once steroids have fulfilled their biological function,
they are broken down by enzymes known as steroid
sulfatases and sulfotransferases. This process, known as catabolism,
converts the steroids into inactive metabolites that can be safely excreted from the body.
The excretion of sterols is a critical step in maintaining homeostasis and preventing the buildup of potentially harmful levels of these
molecules.
## Isolation, structure determination, and methods of analysis
The isolation and structural determination of steroids are essential for understanding their
biological roles and developing new therapies. Techniques
such as chromatography, mass spectrometry, and nuclear magnetic resonance (NMR) spectroscopy are commonly used to isolate and analyze steroidal compounds.
These methods allow researchers to identify unknown steroids or study the structure of
known molecules in detail.
## Chemical synthesis
The chemical synthesis of steroids involves the use of organic chemistry techniques to construct
these molecules from simpler precursors. While natural methods dominate in biological contexts, synthetic
approaches have been developed for the purposes
of research and drug development. Synthesis can be challenging due to the complexity of
the steroid framework, but advanced methodologies have made it possible to create sterols
with specific structural modifications.
### Precursors
The synthesis of steroids begins with precursors such as mevalonic
acid or isopentenyl pyrophosphate (IPP), which are derived from
acetyl-CoA. These compounds undergo a series of enzymatic reactions to produce the steroid nucleus, the core structure of all sterols.
### Semisynthesis
Semisynthesis involves the chemical manipulation of
naturally occurring steroids or their derivatives to create new molecules
with desired properties. This approach is particularly useful
for modifying existing sterols to enhance their biological activity or improve their pharmacokinetics.
### Total synthesis
Total synthesis refers to the de novo construction of steroids from non-steroidal precursors, without relying on natural sources.
This method is often used in drug discovery to create molecules with
therapeutic potential. The challenge lies in replicating the complex structure and biological activity of
naturally occurring sterols.
## Research awards
Over the years, significant research has been conducted
into the chemistry, biology, and applications of steroids.
Notable scientists in this field have received awards for
their contributions to understanding steroid metabolism, biosynthesis, and function. These achievements have led to advancements
in fields such as medicine, nutrition, and pharmacology.
## See also
– **Lipid metabolism**
– **Endocrinology**
– **Biochemistry**
## References
This article is based on publicly available information and does not
constitute medical advice. Always consult a healthcare professional
for medical concerns or before starting any new treatment regimen.
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