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Is dysfunction of the tissue plasminogen activator (tPA)-plasmin pathway a link between major depression and
Sheue-Jane Hou1, Feng-Chang Yen, Shih-Jen Tsai
1Division of Psychiatry, Cheng-Hsin Rehabilitation and Medical Center, Taipei, Taiwan, Republic of China.
Insights
Major depressive disorder (MDD) is a risk factor for cardiovascular disease (CVD). The tissue-type plasminogen activator (tPA)-plasmin pathway may link MDD and CVD, offering new management strategies.
Area of Science:
- Neuroscience
- Cardiology
- Psychiatry
Background:
- Major depressive disorder (MDD) and cardiovascular disease (CVD) are epidemiologically linked.
- MDD is a risk factor for CVD, and patients with both conditions face increased cardiac event risk.
- The underlying mechanisms connecting MDD and CVD remain largely unknown.
Purpose of the Study:
- To explore the potential role of the tissue-type plasminogen activator (tPA)-plasmin pathway in the comorbidity of MDD and CVD.
- To investigate how tPA and its related pathways might mediate the interaction between depression and heart disease.
Main Methods:
- Review of epidemiological, genetic, and clinical studies.
- Examination of preclinical and clinical evidence on the tPA-plasmin system and brain-derived neurotrophic factor (BDNF).
- Analysis of proposed mediating factors such as stress, smoking, inactivity, and inflammation.
Main Results:
- The tPA-plasmin proteolytic cascade is involved in stress response and depression.
- tPA plays a role in cleaving pro-brain-derived neurotrophic factor (proBDNF) to BDNF, influencing its action.
- Dysfunction in the tPA-plasmin pathway is proposed as a potential link between MDD and CVD.
Conclusions:
- The tPA-plasmin pathway dysfunction may contribute to the association between MDD and CVD.
- Further research into the tPA-plasminogen system in comorbid patients could yield novel insights.
- Investigating this pathway may lead to new therapeutic strategies for managing MDD and CVD.
Abstract:
Epidemiological, genetic and clinical studies have demonstrated an association between major depressive disorder (MDD) and cardiovascular disease (CVD). For example, MDD is a risk factor for the development of CVD, while around one fifth of patients with CVD have MDD and a significantly larger percentage have subsyndromal symptoms of depression. Furthermore, patients with CVD and depression have an increased risk of future cardiac events compared to similar cohorts without depression, independent of baseline cardiac dysfunction. Despite evidence that CVD and MDD are epidemiologically linked, the cause of this correlation is still unknown. Several risk factors including physical and psychological stress, smoking, physical inactivity and inflammation have been proposed to mediate the interaction between MDD and CVD. The tissue-type plasminogen activator (tPA)-plasminogen proteolytic cascade is widely expressed in the brain. Accumulating evidence from preclinical and clinical studies suggests that tPA and its inhibitor, plasminogen activator inhibitor-1, are related to stress reaction and depression. In addition, brain-derived neurotrophic factor (BDNF) is important for the pathogenesis of MDD and the tPA-plasminogen proteolytic cascade has been implicated in the cleavage of proBDNF to BDNF in the brain, by which the direction of BDNF action is controlled. Thus, it is proposed that tPA-plasmin pathway dysfunction may play a role in the link between MDD and CVD. Future study of the components in the tPA-plasminogen system in CVD patients comorbid with MDD may lead to new, potentially important insights into the link between MDD and CVD, and might also contribute to novel strategies for the management of these two common and devastating diseases.
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