在黑色皮质素系统的发展和功能中的性二态化
Marc Claret1,2,3, Roberta Haddad-Tóvolli4
1Neuronal Control of Metabolism (NeuCoMe) Laboratory, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Reviews in endocrine & metabolic disorders
|June 24, 2025
概括
黑色皮质素系统中的性别差异会影响能量平衡和新陈代谢. 了解这些变异对于开发针对肥胖和代谢障碍的向疗法至关重要.
科学领域:
- 神经内分泌学神经内分泌学
- 代谢调节 代谢调节 代谢调节
- 在生理学的性别差异.
背景情况:
- 黑色皮质素系统,涉及亲opiomelanocortin (POMC) 和agouti相关 (AgRP) 神经元,对于能量稳定至关重要.
- 在这个系统中存在显著的解剖学和功能性差异,影响了代谢适应.
- 这些差异受到性激素,遗传学,环境和神经电路的影响.
研究的目的:
- 审查有关黑色皮质素系统发育和功能性差异的当前知识.
- 探索这些差异如何促进代谢的性别二态控制.
- 强调在代谢研究和临床实践中将性别视为变量的重要性.
主要方法:
- 对调查黑色皮质素系统和性别差异的研究进行文献综述.
- 对神经电路,荷尔蒙影响和遗传/环境因素的研究分析.
- 综合了与代谢适应,食欲和能量消耗有关的发现.
主要成果:
- 黑色皮质素系统表现出不同的男性和女性调节机制.
- 这些性别特定的途径影响食欲,能量消耗和对代谢障碍的易感性.
- 性差异是由荷尔蒙环境,遗传学和神经组织所塑造的.
结论:
- 黑色皮质素系统中的性别差异对于理解性别二态代谢至关重要.
- 纳入性别作为一个变量对于推动代谢研究和临床研究至关重要.
- 阐明这些机制可以导致更精确的代谢障碍和肥胖的治疗策略.
相关概念视频
The Ratio of X Chromosome to Autosomes
8.8K
In most organisms, sex is determined by the ratio of X and Y chromosomes. However, in some organisms, such as Drosophila and C.elegans, sex is determined by the ratio of the number of X chromosomes to the number of sets of autosomes. The Y chromosome in Drosophila is active but does not determine sex. It contains genes responsible for the production of sperms in adult flies.
Normal male Drosophila has a ratio of one X chromosome to two sets of autosomes. In contrast, normal female...
Normal male Drosophila has a ratio of one X chromosome to two sets of autosomes. In contrast, normal female...
8.8K
Background and Environment Affect Phenotype
6.7K
Although the genetic makeup of an organism plays a major role in determining the phenotype, there are also several environmental factors, such as temperature, oxygen availability, presence of mutagens, that can alter an organism’s phenotype.
An example of how genetic background affects phenotype can be seen in horses. The Extension gene in horses is responsible for their coat color. A wild-type gene (EE) produces black pigment in the coat, while a mutant gene (ee) produces red pigment. A...
An example of how genetic background affects phenotype can be seen in horses. The Extension gene in horses is responsible for their coat color. A wild-type gene (EE) produces black pigment in the coat, while a mutant gene (ee) produces red pigment. A...
6.7K
Dosage Compensation
6.3K
In animals, gender is determined by the number and type of sex chromosome. For example, human females have two X chromosomes, and males have one X and one Y chromosome, whereas C.elegans with one X chromosome is a male, and the one with two X chromosomes is a hermaphrodite.
In addition to sexual development, the X chromosome has genes involved in autosomal functions such as brain development and the immune system. Therefore, males and females with distinct numbers of X chromosomes will...
In addition to sexual development, the X chromosome has genes involved in autosomal functions such as brain development and the immune system. Therefore, males and females with distinct numbers of X chromosomes will...
6.3K
Pigmentation
2.8K
The color of the skin is influenced by a number of pigments, including melanin, carotene, and hemoglobin. Recall that melanin is produced by cells called melanocytes, which are found scattered throughout the stratum basale of the epidermis. The melanin is transferred to the keratinocytes via melanosomes.
Melanin occurs in two primary forms: eumelanin that provides black and brown pigment and pheomelanin that provides red color. Dark-skinned individuals produce more melanin than those with pale...
Melanin occurs in two primary forms: eumelanin that provides black and brown pigment and pheomelanin that provides red color. Dark-skinned individuals produce more melanin than those with pale...
2.8K
Epistasis
47.8K
In addition to multiple alleles at the same locus influencing traits, numerous genes or alleles at different locations may interact and influence phenotypes in a phenomenon called epistasis. For example, rabbit fur can be black or brown depending on whether the animal is homozygous dominant or heterozygous at a TYRP1 locus. However, if the rabbit is also homozygous recessive at a locus on the tyrosinase gene (TYR), it will have an unshaded coat that appears white, regardless of its TYRP1...
47.8K
Pleiotropy
41.2K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
41.2K


