Department of Internal Medicine, School of Medical Science, University of Campinas (UNICAMP), Campinas, SP, Brazil.
Department of Radiology, University of Campinas (UNICAMP), Campinas, SP, Brazil.
Front Endocrinol (Lausanne). 2023 Aug 10;14:1172835. doi: 10.3389/fendo.2023.1172835. eCollection 2023.
Cdc2-like kinase (CLK2) is a member of CLK kinases expressed in hypothalamic neurons and is activated in response to refeeding, leptin, or insulin. Diet-induced obesity and leptin receptor-deficient mice lack CLK2 signal in the hypothalamic neurons. The neurotransmiter gamma-aminobutyric acid (GABA) is among the most prevalent in the central nervous system (CNS), particularly in the hypothalamus. Given the abundance of GABA-expressing neurons and their potential influence on regulating energy and behavioral homeostasis, we aimed to explore whether the deletion of CLK2 in GABAergic neurons alters energy homeostasis and behavioral and cognitive functions in both genders of mice lacking CLK2 in Vgat-expressing neurons (Vgat-Cre; Clk2) on chow diet.
We generated mice lacking Clk2 in Vgat-expressing neurons (Vgat-Cre; Clk2) by mating Clk2 mice with Vgat-IRES-Cre transgenic mice and employed behavior, and physiological tests, and molecular approaches to investigate energy metabolism and behavior phenotype of both genders.
We showed that deletion of CLK2 in GABAergic neurons increased adiposity and food intake in females. The mechanisms behind these effects were likely due, at least in part, to hypothalamic insulin resistance and upregulation of hypothalamic Npy and Agrp expression. Besides normal insulin and pyruvate sensitivity, Vgat-Cre; Clk2 females were glucose intolerant. Male Vgat-Cre; Clk2 mice showed an increased energy expenditure (EE). Risen EE may account for avoiding weight and fat mass gain in male Vgat-Cre; Clk2 mice. Vgat-Cre; Clk2 mice had no alteration in cognition or memory functions in both genders. Interestingly, deleting CLK2 in GABAergic neurons changed anxiety-like behavior only in females, not males. These findings suggest that CLK2 in GABAergic neurons is critical in regulating energy balance and anxiety-like behavior in a gender-specific fashion and could be a molecular therapeutic target for combating obesity associated with psychological disorders in females.
Cdc2 样激酶 (CLK2) 是在下丘脑神经元中表达的 CLK 激酶家族的成员,它在重新进食、瘦素或胰岛素的刺激下被激活。饮食诱导的肥胖和瘦素受体缺陷的小鼠在下丘脑神经元中缺乏 CLK2 信号。神经递质γ-氨基丁酸 (GABA) 是中枢神经系统 (CNS) 中最常见的神经递质之一,特别是在下丘脑。鉴于 GABA 表达神经元的丰富性及其对调节能量和行为平衡的潜在影响,我们旨在探索在缺乏 Vgat 表达神经元中 CLK2 的小鼠 (Vgat-Cre; Clk2) 上,GABA 能神经元中 CLK2 的缺失是否会改变能量平衡以及雄性和雌性小鼠的行为和认知功能。
我们通过将 Clk2 小鼠与 Vgat-IRES-Cre 转基因小鼠交配,生成了在 Vgat 表达神经元中缺乏 Clk2 的小鼠 (Vgat-Cre; Clk2),并采用行为和生理测试以及分子方法来研究雌雄两性的能量代谢和行为表型。
我们发现,GABA 能神经元中 CLK2 的缺失会增加雌性肥胖和食物摄入。这些影响的机制可能至少部分归因于下丘脑胰岛素抵抗和下丘脑 Npy 和 Agrp 表达的上调。除了正常的胰岛素和丙酮酸敏感性外,Vgat-Cre; Clk2 雌性小鼠表现出葡萄糖不耐受。雄性 Vgat-Cre; Clk2 小鼠的能量消耗 (EE) 增加。升高的 EE 可能解释了雄性 Vgat-Cre; Clk2 小鼠避免体重和脂肪量增加的原因。Vgat-Cre; Clk2 小鼠在雌雄两性的认知或记忆功能上均无改变。有趣的是,GABA 能神经元中 CLK2 的缺失仅在雌性小鼠中改变了焦虑样行为,而在雄性小鼠中没有改变。这些发现表明,GABA 能神经元中的 CLK2 以性别特异性的方式在调节能量平衡和焦虑样行为方面至关重要,并且可能成为治疗女性肥胖相关心理障碍的分子治疗靶点。