Placental lactogen Iγ, a variant of the placental lactogen (PL) hormone, plays a multifaceted role during pregnancy, akin to its closely related counterparts in the prolactin/growth hormone family. Synthesized predominantly by the syncytiotrophoblast cells within the placenta, Placental lactogen Iγ serves as a critical mediator in the complex orchestration of maternal and fetal physiological adaptations throughout gestation.The actions of Placental lactogen Iγ are diverse, reflecting its structural homology to both prolactin (PRL) and growth hormone (GH). Its involvement in metabolic regulation is paramount, as it aids in ensuring sufficient glucose availability for the developing fetus. By promoting lipolysis, Placental lactogen Iγ elevates free fatty acid levels in maternal blood, which can be utilized as an alternative energy source, thereby sparing glucose for fetal use. Additionally, it has been implicated in the modulation of insulin sensitivity, contributing to gestational diabetogenic effects that favor fetal nutrient supply.
Beyond its metabolic contributions, Placental lactogen Iγ also influences mammary gland development, preparing the mother's breasts for milk production and lactation after childbirth. It achieves this by stimulating the growth of mammary ducts and alveoli, as well as by inducing the expression of enzymes critical for milk synthesis, thereby complementing the actions of estrogen and progesterone during pregnancy.On a molecular level, Placental lactogen Iγ achieves its biological effects by interacting with PRL and GH receptors on target tissues, triggering a cascade of intracellular signaling pathways that govern growth, metabolism, and developmental processes. An imbalance in Placental lactogen Iγ levels can have significant repercussions, potentially leading to gestational complications or influencing fetal growth patterns, underscoring its importance in the maintenance of a healthy pregnancy.
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제품명 | CAS # | 카탈로그 번호 | 수량 | 가격 | 引用 | RATING |
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Bromocriptine | 25614-03-3 | sc-337602A sc-337602B sc-337602 | 10 mg 100 mg 1 g | $56.00 $260.00 $556.00 | 4 | |
뇌하수체의 프로락틴 분비를 억제하여 잠재적으로 프로락틴 계열의 활동에 영향을 미치는 도파민 D2 수용체 작용제입니다. | ||||||
Cabergoline | 81409-90-7 | sc-203864 sc-203864A | 10 mg 50 mg | $300.00 $1055.00 | ||
브로모크립틴과 마찬가지로 지속성 도파민 수용체 작용제로서 프로락틴 수치를 감소시켜 프로락틴 가족 구성원의 활동에 잠재적으로 영향을 미칩니다. | ||||||
Dopamine | 51-61-6 | sc-507336 | 1 g | $290.00 | ||
자연적으로 프로락틴 억제 인자로 작용하여 특정 프로락틴 계열의 발현 또는 작용을 잠재적으로 감소시킵니다. | ||||||
Metergoline | 17692-51-2 | sc-204079 sc-204079A | 10 mg 50 mg | $78.00 $286.00 | ||
세로토닌 및 도파민 수용체 길항제로, 특정 조건에서 프로락틴 수치를 감소시키는 것으로 나타났습니다. | ||||||
Ropinirole Hydrochloride | 91374-20-8 | sc-205843 sc-205843A | 25 mg 100 mg | $82.00 $311.00 | 1 | |
또한 도파민 작용제 작용으로 인해 프로락틴 수치를 낮출 수 있습니다. | ||||||
(S)-Pramipexole Dihydrochloride | 104632-25-9 | sc-212895 | 10 mg | $164.00 | ||
프로락틴 수치를 낮출 수 있는 또 다른 도파민 수용체 작용제입니다. | ||||||
Domperidone | 57808-66-9 | sc-203032 sc-203032A | 50 mg 250 mg | $60.00 $281.00 | 2 | |
주로 도파민 D2 수용체 길항제이지만, 프로락틴 수치를 높이는 데 사용되지만 프로락틴 신호 경로와 복잡한 상호작용을 할 수 있습니다. |